Gene Details



INPP5E and homologs in 3 species are found in 654 GeneSets:


- Entrez   - Ensembl   - GeneNetwork   - STRING   - Allen Brain Atlas   - Comparative Toxicogenomics Database  

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier I Mouse MP 1350 Genes GS165707: MP:0000428 abnormal craniofacial morphology
Expand Tier I Mouse GO 7755 Genes GS185131: GO:0044699 single-organism process
Expand Tier I Mouse MP 47 Genes GS168997: MP:0009640 abnormal renal tubule epithelium morphology
Expand Tier I Mouse GO 254 Genes GS184027: GO:0006066 alcohol metabolic process
Expand Tier I Mouse MP 21 Genes GS165342: MP:0001890 anencephaly
Expand Tier I Human GO 250 Genes GS205884: GO:0016311 dephosphorylation
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 6 Genes GS174960: HP:0011932 Abnormality of the superior cerebellar peduncle
Expand Tier I Mouse GO 12 Genes GS188385: GO:0034593 phosphatidylinositol bisphosphate phosphatase activity
Expand Tier I Human 99 Genes GS175130: HP:0000750 Delayed speech and language development
Expand Tier I Mouse MP 3631 Genes GS169830: MP:0005384 cellular phenotype
Expand Tier I Mouse GO 1822 Genes GS190997: GO:0044281 small molecule metabolic process
Expand Tier I Human 269 Genes GS172261: HP:0000357 Abnormal location of ears
Expand Tier I Human 5 Genes GS172633: HP:0002871 Central apnea
Expand Tier I Human 845 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human CTD 200 Genes GS125369: Lamivudine interacting genes (MeSH:D019259) in CTD
Expand Tier I Mouse MP 521 Genes GS165382: MP:0001260 increased body weight
Expand Tier I Mouse MP 192 Genes GS166394: MP:0003728 abnormal retinal photoreceptor layer morphology
Expand Tier I Human GO 15 Genes GS202709: GO:0052745 inositol phosphate phosphatase activity
Expand Tier II Mouse 378 Genes GS36049: Neocortex Gene expression correlates of Light- Dark Box Total seconds spent in light compartment in Females & Males BXD
Expand Tier I Mouse MP 546 Genes GS167046: MP:0003881 abnormal nephron morphology
Expand Tier I Human 17 Genes GS172643: HP:0002365 Hypoplasia of the brainstem
Expand Tier I Mouse MP 385 Genes GS166406: MP:0002110 abnormal digit morphology
Expand Tier I Human 70 Genes GS175439: HP:0009136 Duplication involving bones of the feet
Expand Tier I Human 178 Genes GS176151: HP:0000256 Macrocephaly
Expand Tier I Human 491 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Human 360 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Human 135 Genes GS170969: HP:0000157 Abnormality of the tongue
Expand Tier I Human 157 Genes GS172363: HP:0004324 Increased body weight
Expand Tier II Mouse 60 Genes GS35675: Whole Brain Gene expression correlates of Morphine photocell counts minutes 75-90 in Males BXD
Expand Tier I Mouse MP 679 Genes GS170021: MP:0011087 complete neonatal lethality
Expand Tier I Human 786 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 38 Genes GS176220: HP:0011620 Abnormality of abdominal situs
Expand Tier I Human 222 Genes GS173995: HP:0000508 Ptosis
Expand Tier I Human GO 236 Genes GS206874: GO:0006650 glycerophospholipid metabolic process
Expand Tier II Mouse 58 Genes GS36697: Whole Brain Gene expression correlates of Morphine Vertical Activity 30-45 min in Females BXD
Expand Tier II Mouse 36 Genes GS35705: Whole Brain Gene expression correlates of Morphine distance (cm) travelled minutes 105-120 in Males BXD
Expand Tier I Human 426 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Mouse MP 123 Genes GS166938: MP:0002828 abnormal renal glomerular capsule morphology
Expand Tier I Human GO 440 Genes GS209602: GO:0051960 regulation of nervous system development
Expand Tier I Human 69 Genes GS172825: HP:0001829 Polydactyly (feet)
Expand Tier I Mouse 543 Genes GS136612: colon tumor susceptibility 2 (Scc2, Published QTL Chr 2)
Expand Tier II Mouse 91 Genes GS35700: Whole Brain Gene expression correlates of Morphine distance (cm) travelled minutes 105-120 in Females BXD
Expand Tier I Human 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Mouse GO 8406 Genes GS177404: GO:0005737 cytoplasm
Expand Tier I Mouse GO 3080 Genes GS177265: GO:0048731 system development
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier II Mouse 63 Genes GS36702: Whole Brain Gene expression correlates of Morphine Vertical Activity 30-45 min in Males BXD
Expand Tier I Mouse GO 3615 Genes GS178359: GO:0071840 cellular component organization or biogenesis
Expand Tier I Mouse GO 2955 Genes GS181893: GO:0048522 positive regulation of cellular process
Expand Tier I Mouse GO 3597 Genes GS188142: GO:0048856 anatomical structure development
Expand Tier I Human 66 Genes GS176263: HP:0100259 Postaxial polydactyly
Expand Tier II Mouse 456 Genes GS84122: ethanol conditioned taste aversion (Published QTL, Chr 2)
Expand Tier I Mouse MP 700 Genes GS165194: MP:0001533 abnormal skeleton physiology
Expand Tier I Mouse MP 1350 Genes GS165228: MP:0005382 craniofacial phenotype
Expand Tier I Mouse MP 257 Genes GS170425: MP:0004508 abnormal pectoral girdle bone morphology
Expand Tier I Mouse MP 1008 Genes GS164333: MP:0000516 abnormal renal/urinary system morphology
Expand Tier I Human 117 Genes GS172063: HP:0000107 Renal cysts
Expand Tier I Human 46 Genes GS172570: HP:0000341 Narrow forehead
Expand Tier I Human GO 1010 Genes GS196988: GO:0045595 regulation of cell differentiation
Expand Tier I Human GO 258 Genes GS195576: GO:0016791 phosphatase activity
Expand Tier I Mouse GO 2762 Genes GS178357: GO:0071842 cellular component organization at cellular level
Expand Tier I Human 202 Genes GS176242: HP:0004207 Abnormality of the 5th finger
Expand Tier I Human GO 4371 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Human 456 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Mouse MP 2357 Genes GS163824: MP:0001259 abnormal body weight
Expand Tier I Human 6 Genes GS172511: HP:0002335 Agenesis of cerebellar vermis
Expand Tier I Mouse GO 912 Genes GS179236: GO:0048699 generation of neurons
Expand Tier I Human GO 18 Genes GS198911: GO:0046839 phospholipid dephosphorylation
Expand Tier I Human 123 Genes GS173242: HP:0001337 Tremor
Expand Tier I Mouse MP 331 Genes GS163432: MP:0006069 abnormal retinal neuronal layer morphology
Expand Tier I Human 13 Genes GS172095: HP:0000588 Optic nerve coloboma
Expand Tier II Mouse 109 Genes GS35680: Whole Brain Gene expression correlates of Morphine distance (cm) travelled minutes 90-105 in Females & Males BXD
Expand Tier II Mouse 69 Genes GS33944: Whole Brain Gene expression correlates of Morphine distance (cm) travelled minutes 120-135 in Females & Males BXD
Expand Tier I Mouse 459 Genes GS135533: cobblestone area-forming cell number QTL 1 (Cafcnq1, Published QTL Chr 2)
Expand Tier I Mouse MP 994 Genes GS168502: MP:0002058 neonatal lethality
Expand Tier I Human 101 Genes GS175263: HP:0001161 Polydactyly (hands)
Expand Tier I Human 741 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 69 Genes GS176437: HP:0002334 Abnormality of the cerebellar vermis
Expand Tier I Human 260 Genes GS170933: HP:0001288 Gait disturbance
Expand Tier I Human 489 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Mouse GO 1209 Genes GS178284: GO:0031090 organelle membrane
Expand Tier I Human 36 Genes GS172842: HP:0000480 Retinal coloboma
Expand Tier I Human GO 541 Genes GS196667: GO:0008610 lipid biosynthetic process
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 1770 Genes GS194455: GO:0051239 regulation of multicellular organismal process
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human GO 346 Genes GS202602: GO:0006644 phospholipid metabolic process
Expand Tier I Human 19 Genes GS175110: HP:0000570 Abnormality of saccadic eye movements
Expand Tier I Human 51 Genes GS171787: HP:0001395 Hepatic fibrosis
Expand Tier I Human 179 Genes GS176589: HP:0001273 Abnormality of the corpus callosum
Expand Tier I Mouse GO 80 Genes GS181135: GO:0010976 positive regulation of neuron projection development
Expand Tier I Mouse MP 399 Genes GS167615: MP:0003935 abnormal craniofacial development
Expand Tier I Mouse MP 258 Genes GS169057: MP:0000914 exencephaly
Expand Tier I Mouse 548 Genes GS136471: periosteal circumference and femur length 1 (Pcfm1, Published QTL Chr 2)
Expand Tier I Mouse GO 244 Genes GS179362: GO:0005929 cilium
Expand Tier I Human GO 1771 Genes GS196284: GO:0012505 endomembrane system
Expand Tier I Mouse GO 12 Genes GS184537: GO:0071545 inositol phosphate catabolic process
Expand Tier I Human 534 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier I Mouse 548 Genes GS135816: ethanol induced ataxia 3 (Etax3, Published QTL Chr 2)
Expand Tier I Human 36 Genes GS174701: HP:0000556 Retinal dystrophy
Expand Tier I Human GO 3125 Genes GS197892: GO:0043228 non-membrane-bounded organelle
Expand Tier I Mouse MP 1183 Genes GS166409: MP:0002114 abnormal axial skeleton morphology
Expand Tier I Mouse GO 2565 Genes GS192299: GO:0006793 phosphorus metabolic process
Expand Tier I Human GO 1096 Genes GS208716: GO:2000026 regulation of multicellular organismal development
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Mouse GO 1079 Genes GS178401: GO:0019637 organophosphate metabolic process
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Mouse GO 224 Genes GS188750: GO:0044431 Golgi apparatus part
Expand Tier I Human 179 Genes GS171047: HP:0008736 Hypoplasia of penis
Expand Tier I Human 154 Genes GS175880: HP:0007370 Aplasia/Hypoplasia of the corpus callosum
Expand Tier I Mouse MP 105 Genes GS167521: MP:0005306 abnormal phalanx morphology
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier I Human GO 700 Genes GS205439: GO:0031175 neuron projection development
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier III Mouse 6105 Genes GS213074: Genes with suggestive difference in (B6PF1) vs (PB6F1 + B6 + PWD) comparison
Expand Tier III Mouse 8003 Genes GS213041: Expression profiles of aging in C57BL/6 mouse hippocampal tissue
Expand Tier I Mouse MP 18 Genes GS165346: MP:0009883 palatal shelf hypoplasia
Expand Tier I Mouse MP 1402 Genes GS169832: MP:0005381 digestive/alimentary phenotype
Expand Tier I Human 249 Genes GS176844: HP:0000429 Abnormality of the nasal alae
Expand Tier I Human GO 2511 Genes GS207903: GO:0044281 small molecule metabolic process
Expand Tier I Human 579 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human 281 Genes GS176231: HP:0010938 Abnormality of the external nose
Expand Tier I Human GO 553 Genes GS205302: GO:0000139 Golgi membrane
Expand Tier I Mouse MP 558 Genes GS170680: MP:0003744 abnormal orofacial morphology
Expand Tier I Human 60 Genes GS174300: HP:0000718 Aggressive behavior
Expand Tier I Human GO 11 Genes GS201341: GO:0071545 inositol phosphate catabolic process
Expand Tier II Mouse 405 Genes GS34243: Neocortex Gene expression correlates of Light-Dark Box Percentage time in light in Males BXD
Expand Tier I Human 17 Genes GS175676: HP:0007362 Aplasia/Hypoplasia of the brainstem
Expand Tier II Mouse 53 Genes GS35525: Whole Brain Gene expression correlates of Morphine photocell counts minutes 90-105 in Males BXD
Expand Tier I Human 403 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Mouse 469 Genes GS136890: voluntary alcohol consumption QTL 4 (Vacq4, Published QTL Chr 2)
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Mouse GO 2190 Genes GS191129: GO:0016787 hydrolase activity
Expand Tier I Human 110 Genes GS172484: HP:0009997 Duplication of phalanx of hand
Expand Tier I Mouse GO 639 Genes GS192628: GO:0048666 neuron development
Expand Tier I Mouse GO 786 Genes GS179519: GO:0012505 endomembrane system
Expand Tier I Mouse MP 857 Genes GS166118: MP:0002109 abnormal limb morphology
Expand Tier I Human GO 4097 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Mouse MP 3716 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier I Human 123 Genes GS171946: HP:0002269 Abnormality of neuronal migration
Expand Tier I Human 358 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Human 472 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Mouse MP 384 Genes GS165361: MP:0004624 abnormal thoracic cage morphology
Expand Tier I Mouse GO 8386 Genes GS189751: GO:0050794 regulation of cellular process
Expand Tier I Human 364 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human GO 1852 Genes GS209010: GO:1901575 organic substance catabolic process
Expand Tier I Mouse MP 437 Genes GS163318: MP:0000521 abnormal kidney cortex morphology
Expand Tier I Mouse 3115 Genes GS128575: Ethanol induced LORR Chr# 2
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 699 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Mouse GO 8942 Genes GS185492: GO:0050789 regulation of biological process
Expand Tier I Human 544 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 17 Genes GS173187: HP:0007772 Impaired smooth pursuit
Expand Tier I Mouse GO 781 Genes GS184010: GO:0030030 cell projection organization
Expand Tier II Mouse 385 Genes GS36029: Neocortex Gene expression correlates of Light-Dark Box Total seconds spent in dark compartment in Males BXD
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 2 Genes GS172232: HP:0002195 Dysgenesis of the cerebellar vermis
Expand Tier I Human 512 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Mouse GO 5892 Genes GS180036: GO:0032501 multicellular organismal process
Expand Tier I Mouse GO 825 Genes GS187237: GO:0030182 neuron differentiation
Expand Tier I Human GO 8622 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Mouse GO 5103 Genes GS192512: GO:0003824 catalytic activity
Expand Tier I Human GO 8 Genes GS194970: GO:0046030 inositol trisphosphate phosphatase activity
Expand Tier I Mouse MP 118 Genes GS169298: MP:0009655 abnormal secondary palate development
Expand Tier I Mouse MP 242 Genes GS166294: MP:0011109 partial lethality throughout fetal growth and development
Expand Tier I Human GO 7808 Genes GS207616: GO:0016020 membrane
Expand Tier I Human 784 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier II Mouse 54 Genes GS36677: Whole Brain Gene expression correlates of Morphine vertical activity counts minutes 15-30 in Females & Males BXD
Expand Tier I Mouse GO 3614 Genes GS180229: GO:0005886 plasma membrane
Expand Tier I Human GO 1724 Genes GS198004: GO:0007399 nervous system development
Expand Tier I Mouse GO 1166 Genes GS191779: GO:2000026 regulation of multicellular organismal development
Expand Tier I Human 534 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier I Mouse 338 Genes GS129163: proteoglycan induced spondylitis 2 (Pgis2 Published QTL Chr 2)
Expand Tier I Mouse MP 3437 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Mouse GO 943 Genes GS177094: GO:0006629 lipid metabolic process
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human 72 Genes GS171658: HP:0000612 Iris coloboma
Expand Tier I Human GO 216 Genes GS196055: GO:0008654 phospholipid biosynthetic process
Expand Tier I Human 61 Genes GS175264: HP:0001162 Postaxial polydactyly (hands)
Expand Tier I Mouse GO 666 Genes GS179132: GO:0044255 cellular lipid metabolic process
Expand Tier I Mouse GO 609 Genes GS185024: GO:0044463 cell projection part
Expand Tier II Mouse 85 Genes GS35535: Whole Brain Gene expression correlates of Morphine photocell counts minutes 105-120 in Females BXD
Expand Tier I Human GO 3513 Genes GS193991: GO:0048731 system development
Expand Tier I Human GO 474 Genes GS200117: GO:0051130 positive regulation of cellular component organization
Expand Tier I Human 4 Genes GS175631: HP:0100951 Enlarged fossa interpeduncularis
Expand Tier I Mouse GO 11 Genes GS190065: GO:0046855 inositol phosphate dephosphorylation
Expand Tier I Mouse 446 Genes GS135721: variability in response to cholestrol enriched atherogenic diet (Diet1, Published QTL Chr 2)
Expand Tier I Mouse MP 290 Genes GS168654: MP:0000111 cleft palate
Expand Tier I Mouse GO 14 Genes GS193068: GO:0046174 polyol catabolic process
Expand Tier I Human 6 Genes GS173139: HP:0002418 Abnormality of the midbrain
Expand Tier I Mouse 333 Genes GS135244: adiposity 10 (Adip10, Published QTL Chr 2)
Expand Tier I Human 298 Genes GS174145: HP:0005918 Abnormality of phalanx of finger
Expand Tier I Human GO 238 Genes GS196129: GO:0005929 cilium
Expand Tier I Mouse MP 4173 Genes GS165527: MP:0005378 growth/size phenotype
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human 35 Genes GS171655: HP:0000611 Choroid coloboma
Expand Tier I Mouse MP 28 Genes GS169385: MP:0004320 split sternum
Expand Tier I Mouse GO 229 Genes GS185770: GO:0006644 phospholipid metabolic process
Expand Tier II Mouse 88 Genes GS36722: Whole Brain Gene expression correlates of Morphine vertical activity counts minutes 60-75 in Females & Males BXD
Expand Tier I Human GO 315 Genes GS201237: GO:0046486 glycerolipid metabolic process
Expand Tier I Human GO 493 Genes GS200286: GO:0060284 regulation of cell development
Expand Tier I Human GO 637 Genes GS201839: GO:0044463 cell projection part
Expand Tier I Human GO 672 Genes GS205609: GO:0044431 Golgi apparatus part
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Human GO 1993 Genes GS207862: GO:0009056 catabolic process
Expand Tier I Mouse 542 Genes GS136087: lean body mass 1 (Lbm1, Published QTL Chr 2)
Expand Tier I Mouse GO 2872 Genes GS178360: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Human 201 Genes GS176660: HP:0000050 Hypoplastic genitalia
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Human GO 519 Genes GS198012: GO:0046434 organophosphate catabolic process
Expand Tier II Mouse 90 Genes GS35685: Whole Brain Gene expression correlates of Morphine distance (cm) travelled minutes 90-105 in Females BXD
Expand Tier I Human 607 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human GO 2373 Genes GS195036: GO:0031090 organelle membrane
Expand Tier I Human 221 Genes GS172288: HP:0000358 Posteriorly rotated ears
Expand Tier I Mouse MP 72 Genes GS167286: MP:0008528 polycystic kidney
Expand Tier I Human 42 Genes GS172670: HP:0002363 Abnormality of the brainstem
Expand Tier I Human GO 59 Genes GS197926: GO:0010976 positive regulation of neuron projection development
Expand Tier I Human GO 17 Genes GS210010: GO:0046174 polyol catabolic process
Expand Tier I Human GO 1263 Genes GS197087: GO:0016310 phosphorylation
Expand Tier I Human 47 Genes GS174712: HP:0002553 Highly arched eyebrow
Expand Tier I Mouse GO 197 Genes GS185584: GO:0044712 single-organism catabolic process
Expand Tier I Human 315 Genes GS176568: HP:0000486 Strabismus
Expand Tier I Human 474 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Mouse GO 6 Genes GS192328: GO:0004439 phosphatidylinositol-4,5-bisphosphate 5-phosphatase activity
Expand Tier I Human GO 135 Genes GS202025: GO:0031346 positive regulation of cell projection organization
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 28 Genes GS173311: HP:0010651 Abnormality of the meninges
Expand Tier I Mouse MP 121 Genes GS167974: MP:0009653 abnormal palate development
Expand Tier II Mouse 473 Genes GS84124: ethanol consumption (Published QTL, Chr 2)
Expand Tier I Human 388 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Mouse GO 7644 Genes GS188399: GO:0044238 primary metabolic process
Expand Tier I Human 514 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human GO 7689 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier II Mouse 55 Genes GS36712: Whole Brain Gene expression correlates of Morphine vertical activity counts minutes 45-60 in Females BXD
Expand Tier I Human 76 Genes GS172219: HP:0010301 Spinal dysraphism
Expand Tier I Human GO 72 Genes GS195616: GO:0032580 Golgi cisterna membrane
Expand Tier I Mouse 550 Genes GS136074: insulin QTL 7 (Insq7, Published QTL Chr 2)
Expand Tier I Human GO 259 Genes GS202414: GO:0044712 single-organism catabolic process
Expand Tier I Mouse MP 21 Genes GS163832: MP:0011065 abnormal kidney epithelial cell primary cilium morphology
Expand Tier I Human GO 3409 Genes GS195113: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier III Mouse 2289 Genes GS216489: Genes that are binding sites of CREB and zif268, transcription factors mediating neuronal activity and plasticity, in Mus musculus.
Expand Tier I Mouse MP 1416 Genes GS164261: MP:0002081 perinatal lethality
Expand Tier I Human 72 Genes GS176835: HP:0000426 Prominent nasal bridge
Expand Tier I Mouse GO 3293 Genes GS186214: GO:0048518 positive regulation of biological process
Expand Tier I Mouse GO 1221 Genes GS187576: GO:0051128 regulation of cellular component organization
Expand Tier I Mouse MP 43 Genes GS164887: MP:0003073 abnormal metacarpal bone morphology
Expand Tier I Human GO 1456 Genes GS205144: GO:0048468 cell development
Expand Tier I Human 64 Genes GS174379: HP:0002084 Encephalocele
Expand Tier II Mouse 69 Genes GS33992: Whole Brain Gene expression correlates of Morphine distance (cm) travelled minutes 75-90 in Females & Males BXD
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 262 Genes GS172033: HP:0000369 Low-set ears
Expand Tier II Mouse 87 Genes GS35665: Whole Brain Gene expression correlates of Morphine photocell counts minutes 75-90 in Females & Males BXD
Expand Tier I Human 442 Genes GS176801: HP:0001263 Global developmental delay
Expand Tier I Human 81 Genes GS171773: HP:0000532 Chorioretinal abnormality
Expand Tier I Human 414 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human GO 137 Genes GS201235: GO:0046488 phosphatidylinositol metabolic process
Expand Tier I Human 92 Genes GS171656: HP:0000610 Abnormality of the choroid
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Mouse MP 1817 Genes GS168149: MP:0005508 abnormal skeleton morphology
Expand Tier I Mouse MP 3110 Genes GS167020: MP:0003956 abnormal body size
Expand Tier I Mouse GO 305 Genes GS189020: GO:0016311 dephosphorylation
Expand Tier I Mouse MP 132 Genes GS169887: MP:0008272 abnormal endochondral bone ossification
Expand Tier I Mouse MP 323 Genes GS170380: MP:0003755 abnormal palate morphology
Expand Tier I Human 163 Genes GS176478: HP:0002119 Ventriculomegaly
Expand Tier II Mouse 101 Genes GS35515: Whole Brain Gene expression correlates of Morphine photocell counts minutes 90-105 in Females & Males BXD
Expand Tier I Mouse MP 77 Genes GS164164: MP:0009887 abnormal palatal shelf fusion at midline
Expand Tier I Human 50 Genes GS176834: HP:0002793 Abnormal respiratory patterns
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Human 553 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier II Mouse 106 Genes GS36587: Whole Brain Gene expression correlates of Morphine vertical activity counts minutes 90-105 in Females & Males BXD
Expand Tier I Human 411 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human GO 258 Genes GS197043: GO:0044282 small molecule catabolic process
Expand Tier I Human GO 1067 Genes GS196002: GO:0048699 generation of neurons
Expand Tier I Human GO 97 Genes GS194400: GO:0006661 phosphatidylinositol biosynthetic process
Expand Tier I Human GO 355 Genes GS198370: GO:0042578 phosphoric ester hydrolase activity
Expand Tier I Mouse MP 1989 Genes GS169530: MP:0005390 skeleton phenotype
Expand Tier I Human 34 Genes GS173140: HP:0011534 Abnormal spatial orientation of the cardiac segments
Expand Tier I Human 291 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier I Mouse MP 185 Genes GS164411: MP:0000562 polydactyly
Expand Tier I Human 46 Genes GS173617: HP:0011220 Prominent forehead
Expand Tier I Human 1006 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Mouse GO 2876 Genes GS182474: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Mouse MP 45 Genes GS163319: MP:0000522 kidney cortex cysts
Expand Tier I Human 13 Genes GS171055: HP:0002342 Intellectual disability, moderate
Expand Tier I Human CTD 377 Genes GS121976: Zidovudine interacting genes (MeSH:D015215) in CTD
Expand Tier I Mouse MP 2485 Genes GS168012: MP:0010832 lethality during fetal growth through weaning
Expand Tier I Human GO 2368 Genes GS207365: GO:0005829 cytosol
Expand Tier I Human 378 Genes GS176038: HP:0002795 Functional respiratory abnormality
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human CTD 223 Genes GS125187: Sulindac interacting genes (MeSH:D013467) in CTD
Expand Tier I Human 81 Genes GS175635: HP:0002251 Aganglionic megacolon
Expand Tier I Human GO 65 Genes GS204325: GO:0019751 polyol metabolic process
Expand Tier I Mouse GO 1451 Genes GS180305: GO:0016310 phosphorylation
Expand Tier I Human GO 231 Genes GS202625: GO:0045017 glycerolipid biosynthetic process
Expand Tier I Human CTD 1148 Genes GS121437: Fluorouracil interacting genes (MeSH:D005472) in CTD
Expand Tier I Human 70 Genes GS171543: HP:0000276 Long face
Expand Tier I Mouse 549 Genes GS136554: pentylenetetrazol induced seizure susceptibility 1b (Ptz1b, Published QTL Chr 2)
Expand Tier I Human GO 12 Genes GS205241: GO:0034593 phosphatidylinositol bisphosphate phosphatase activity
Expand Tier I Human 211 Genes GS173206: HP:0003241 Genital hypoplasia
Expand Tier I Mouse MP 61 Genes GS170285: MP:0004967 abnormal kidney epithelium morphology
Expand Tier I Human 941 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human GO 741 Genes GS208043: GO:0016788 hydrolase activity, acting on ester bonds
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier II Mouse 35 Genes GS36687: Whole Brain Gene expression correlates of Morphine vertical activity counts minutes 15-30 in Males BXD
Expand Tier I Mouse MP 399 Genes GS165567: MP:0008271 abnormal bone ossification
Expand Tier I Mouse MP 14488 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Mouse GO 2538 Genes GS190893: GO:0030154 cell differentiation
Expand Tier I Human GO 4283 Genes GS197009: GO:0005886 plasma membrane
Expand Tier II Mouse 63 Genes GS36622: Whole Brain Gene expression correlates of Morphine vertical activity counts minutes 120-135 in Females BXD
Expand Tier I Human 2 Genes GS175455: HP:0002508 Malformation of brainstem structures
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Tier II Mouse 63 Genes GS35550: Whole Brain Gene expression correlates of Morphine photocell counts minutes 120-135 in Females BXD
Expand Tier I Human 525 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Human 405 Genes GS173743: HP:0001999 Abnormal facial shape
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 470 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier I Human GO 331 Genes GS206569: GO:0045664 regulation of neuron differentiation
Expand Tier I Mouse 338 Genes GS135222: aromatase activity QTL 3 (Aaiq3, Published QTL Chr 2)
Expand Tier I Human 416 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier I Human GO 2824 Genes GS209411: GO:0048869 cellular developmental process
Expand Tier I Mouse GO 9 Genes GS178220: GO:0046030 inositol trisphosphate phosphatase activity
Expand Tier II Mouse 70 Genes GS36692: Whole Brain Gene expression correlates of Morphine Vertical Activity 30-45 min in Females & Males BXD
Expand Tier I Mouse GO 5879 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Human 62 Genes GS172992: HP:0001320 Cerebellar vermis hypoplasia
Expand Tier I Human 5 Genes GS173217: HP:0005957 Breathing dysregulation
Expand Tier I Human 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 409 Genes GS175670: HP:0007364 Aplasia/Hypoplasia of the cerebrum
Expand Tier I Mouse GO 3605 Genes GS190682: GO:0007275 multicellular organismal development
Expand Tier I Human 210 Genes GS175990: HP:0000463 Anteverted nares
Expand Tier I Mouse GO 1681 Genes GS191954: GO:0005856 cytoskeleton
Expand Tier I Mouse 537 Genes GS136515: plasma plant sterol 2a (Plast2a, Published QTL Chr 2)
Expand Tier I Human GO 3307 Genes GS195110: GO:0071842 cellular component organization at cellular level
Expand Tier I Mouse GO 4224 Genes GS193059: GO:0044446 intracellular organelle part
Expand Tier I Human GO 10 Genes GS205244: GO:0034595 phosphatidylinositol phosphate 5-phosphatase activity
Expand Tier I Human 5 Genes GS176393: HP:0011933 Elongated superior cerebellar peduncle
Expand Tier I Human 261 Genes GS176172: HP:0001251 Ataxia
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse GO 18 Genes GS182118: GO:0046839 phospholipid dephosphorylation
Expand Tier I Human 46 Genes GS170961: HP:0000158 Macroglossia
Expand Tier I Mouse GO 8 Genes GS188388: GO:0034595 phosphatidylinositol phosphate 5-phosphatase activity
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Mouse GO 1038 Genes GS180208: GO:0045595 regulation of cell differentiation
Expand Tier I Human GO 209 Genes GS200626: GO:0044262 cellular carbohydrate metabolic process
Expand Tier II Mouse 51 Genes GS36727: Whole Brain Gene expression correlates of Morphine vertical activity counts minutes 60-75 in Females BXD
Expand Tier I Human GO 986 Genes GS204095: GO:0030182 neuron differentiation
Expand Tier I Mouse GO 980 Genes GS188826: GO:0022008 neurogenesis
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier II Mouse 101 Genes GS35545: Whole Brain Gene expression correlates of Morphine photocell counts minutes 120-135 in Females & Males BXD
Expand Tier I Mouse MP 953 Genes GS165160: MP:0006207 embryonic lethality during organogenesis
Expand Tier I Mouse MP 15 Genes GS170534: MP:0011066 abnormal renal tubule epithelial cell primary cilium morphology
Expand Tier I Mouse 459 Genes GS136228: mandible length 2 (Manln2, Published QTL Chr 2)
Expand Tier I Human GO 3125 Genes GS199272: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier I Mouse MP 951 Genes GS165427: MP:0000432 abnormal head morphology
Expand Tier I Human 114 Genes GS173262: HP:0000864 Abnormality of the hypothalamus-pituitary axis
Expand Tier I Human GO 13 Genes GS206950: GO:0046856 phosphatidylinositol dephosphorylation
Expand Tier I Human 529 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human GO 22 Genes GS206952: GO:0046854 phosphatidylinositol phosphorylation
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Mouse GO 165 Genes GS185207: GO:0031346 positive regulation of cell projection organization
Expand Tier I Human 545 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human 160 Genes GS175096: HP:0000286 Epicanthus
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human 215 Genes GS172139: HP:0010993 Abnormality of the cerebral subcortex
Expand Tier I Human 65 Genes GS170884: HP:0006919 Abnormal aggressive, impulsive or violent behavior
Expand Tier II Mouse 378 Genes GS36019: Neocortex Gene expression correlates of Light-Dark Box Total seconds spent in dark compartment in Females & Males BXD
Expand Tier II Mouse 42 Genes GS36742: Whole Brain Gene expression correlates of Morphine vertical activity counts minutes 75-90 in Females BXD
Expand Tier I Human 737 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Mouse MP 9 Genes GS167210: MP:0009744 postaxial polydactyly
Expand Tier II Mouse 385 Genes GS36059: Neocortex Gene expression correlates of Light- Dark Box Total seconds spent in light compartment in Males BXD
Expand Tier I Human 33 Genes GS172620: HP:0000657 Oculomotor apraxia
Expand Tier I Human 81 Genes GS173031: HP:0004362 Abnormality of the enteric ganglia
Expand Tier I Mouse MP 1385 Genes GS163971: MP:0002092 abnormal eye morphology
Expand Tier I Human CTD 5725 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
Expand Tier I Human GO 118 Genes GS201074: GO:0005795 Golgi stack
Expand Tier I Human 203 Genes GS171621: HP:0100851 Abnormal emotion/affect behavior
Expand Tier I Mouse GO 9323 Genes GS180152: GO:0065007 biological regulation
Expand Tier I Mouse MP 1211 Genes GS165536: MP:0005371 limbs/digits/tail phenotype
Expand Tier I Human 21 Genes GS171661: HP:0000617 Abnormality of ocular smooth pursuit
Expand Tier I Human 1 Genes GS171093: HP:0007271 Occipital myelomeningocele
Expand Tier I Human GO 52 Genes GS207989: GO:0035085 cilium axoneme
Expand Tier I Human 23 Genes GS171937: HP:0004346 Increased respiratory rate or depth of breathing
Expand Tier I Mouse 469 Genes GS135851: fecundity QTL 1 (Fecq1, Published QTL Chr 2)
Expand Tier I Human 487 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier I Human 21 Genes GS171403: HP:0001956 Truncal obesity
Expand Tier I Human 3 Genes GS172749: HP:0002436 Occipital meningocele
Expand Tier I Human GO 794 Genes GS209568: GO:0048666 neuron development
Expand Tier II Mouse 98 Genes GS36717: Whole Brain Gene expression correlates of Morphine vertical activity counts minutes 45-60 in Males BXD
Expand Tier I Human GO 1178 Genes GS201075: GO:0005794 Golgi apparatus
Expand Tier I Mouse GO 371 Genes GS189692: GO:0045664 regulation of neuron differentiation
Expand Tier I Human 22 Genes GS173165: HP:0002435 Meningocele
Expand Tier I Human 438 Genes GS173024: HP:0000811 Abnormal external genitalia
Expand Tier I Human GO 4567 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human GO 1434 Genes GS206618: GO:0050793 regulation of developmental process
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human 111 Genes GS171465: HP:0004275 Duplication of hand bones
Expand Tier I Mouse GO 1398 Genes GS181215: GO:0007399 nervous system development
Expand Tier I Human GO 87 Genes GS209547: GO:0031985 Golgi cisterna
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human 530 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human GO 32 Genes GS199561: GO:0043647 inositol phosphate metabolic process
Expand Tier I Human GO 1213 Genes GS204438: GO:0051128 regulation of cellular component organization
Expand Tier I Human 94 Genes GS174879: HP:0002104 Apnea
Expand Tier I Human GO 6769 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human GO 5152 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Tier II Mouse 93 Genes GS34352: Whole Brain Gene expression correlates of Morphine Open Field TOTAL distance (cm) travelled in Females & Males BXD
Expand Tier I Human 20 Genes GS173102: HP:0010808 Protruding tongue
Expand Tier I Mouse MP 574 Genes GS167217: MP:0001325 abnormal retina morphology
Expand Tier I Mouse MP 1848 Genes GS167622: MP:0002152 abnormal brain morphology
Expand Tier I Mouse MP 564 Genes GS170104: MP:0003723 abnormal long bone morphology
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse GO 2876 Genes GS181102: GO:0043228 non-membrane-bounded organelle
Expand Tier I Human GO 397 Genes GS209887: GO:0050767 regulation of neurogenesis
Expand Tier I Human 142 Genes GS171178: HP:0000238 Hydrocephalus
Expand Tier I Mouse MP 187 Genes GS164469: MP:0003675 kidney cysts
Expand Tier I Human GO 6278 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier II Mouse 105 Genes GS34233: Neocortex Gene expression correlates of Light-Dark Box Percentage of distance traveled in light compartment in Males BXD
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 8137 Genes GS202316: GO:0050789 regulation of biological process
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human 599 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Human 2 Genes GS171724: HP:0008915 Childhood-onset truncal obesity
Expand Tier I Human 24 Genes GS174509: HP:0100716 Autoagression
Expand Tier I Mouse MP 158 Genes GS169968: MP:0009890 cleft secondary palate
Expand Tier I Mouse MP 478 Genes GS170351: MP:0006208 lethality throughout fetal growth and development
Expand Tier I Mouse MP 815 Genes GS169062: MP:0000913 abnormal brain development
Expand Tier I Human 324 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Mouse MP 465 Genes GS164665: MP:0000572 abnormal autopod morphology
Expand Tier I Mouse GO 1860 Genes GS177717: GO:0051239 regulation of multicellular organismal process
Expand Tier I Human 344 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Human 398 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier II Mouse 91 Genes GS36602: Whole Brain Gene expression correlates of Morphine vertical activity counts minutes 105-120 in Females & Males BXD
Expand Tier I Human 5 Genes GS172725: HP:0007973 Retinal dysplasia
Expand Tier I Mouse GO 14 Genes GS190064: GO:0046856 phosphatidylinositol dephosphorylation
Expand Tier I Human GO 810 Genes GS195897: GO:0044255 cellular lipid metabolic process
Expand Tier I Human 196 Genes GS172034: HP:0000368 Low-set, posteriorly rotated ears
Expand Tier I Human 197 Genes GS175785: HP:0002500 Abnormality of the cerebral white matter
Expand Tier I Mouse 469 Genes GS135820: ethanol consumption 1 (Etohc1, Published QTL Chr 2)
Expand Tier I Mouse GO 196 Genes GS180264: GO:0044282 small molecule catabolic process
Expand Tier I Mouse GO 41 Genes GS180683: GO:0046164 alcohol catabolic process
Expand Tier I Mouse 448 Genes GS136889: voluntary alcohol consumption QTL 3 (Vacq3, Published QTL Chr 2)
Expand Tier I Human GO 6 Genes GS209265: GO:0004439 phosphatidylinositol-4,5-bisphosphate 5-phosphatase activity
Expand Tier I Mouse MP 756 Genes GS170683: MP:0003743 abnormal facial morphology
Expand Tier I Human 263 Genes GS176145: HP:0001780 Abnormality of toe
Expand Tier I Mouse GO 2710 Genes GS192471: GO:0048869 cellular developmental process
Expand Tier I Human GO 256 Genes GS195002: GO:0031344 regulation of cell projection organization
Expand Tier I Human 16 Genes GS176249: HP:0002789 Tachypnea
Expand Tier I Mouse GO 9049 Genes GS180166: GO:0008152 metabolic process
Expand Tier I Mouse MP 647 Genes GS164446: MP:0005195 abnormal posterior eye segment morphology
Expand Tier I Human 246 Genes GS176806: HP:0003812 Phenotypic variability
Expand Tier I Mouse MP 52 Genes GS164929: MP:0009888 palatal shelves fail to meet at midline
Expand Tier I Human 6 Genes GS173033: HP:0011931 Abnormality of the cerebellar peduncle
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Mouse GO 1006 Genes GS184267: GO:0005794 Golgi apparatus
Expand Tier II Mouse 124 Genes GS34361: Whole Brain Gene expression correlates of Morphine TOTAL vertical activity counts in Females & Males BXD
Expand Tier I Human GO 23 Genes GS198906: GO:0046834 lipid phosphorylation
Expand Tier I Mouse GO 137 Genes GS192255: GO:0030258 lipid modification
Expand Tier II Mouse 61 Genes GS35690: Whole Brain Gene expression correlates of Morphine distance (cm) travelled minutes 90-105 in Males BXD
Expand Tier I Mouse GO 524 Genes GS183321: GO:0051130 positive regulation of cellular component organization
Expand Tier I Mouse GO 555 Genes GS183122: GO:0005975 carbohydrate metabolic process
Expand Tier I Human 1 Genes GS172215: HP:0007910 Retinal dystrophy, congenital, nonprogressive
Expand Tier I Mouse GO 206 Genes GS183826: GO:0044262 cellular carbohydrate metabolic process
Expand Tier I Mouse MP 1476 Genes GS169531: MP:0005391 vision/eye phenotype
Expand Tier I Human 426 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Human 472 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human GO 1138 Genes GS193812: GO:0006629 lipid metabolic process
Expand Tier I Mouse MP 940 Genes GS165876: MP:0002135 abnormal kidney morphology
Expand Tier I Mouse MP 592 Genes GS165809: MP:0002864 abnormal ocular fundus morphology
Expand Tier I Mouse GO 8145 Genes GS190714: GO:0016020 membrane
Expand Tier I Human 263 Genes GS176477: HP:0002118 Abnormality of the cerebral ventricles
Expand Tier I Mouse GO 549 Genes GS183491: GO:0060284 regulation of cell development
Expand Tier I Human GO 19 Genes GS194874: GO:0052866 phosphatidylinositol phosphate phosphatase activity
Expand Tier I Human GO 90 Genes GS209548: GO:0031984 organelle subcompartment
Expand Tier I Human 221 Genes GS171139: HP:0005288 Abnormality of the nares
Expand Tier I Human 588 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human 780 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Mouse GO 1394 Genes GS191552: GO:0042995 cell projection
Expand Tier I Human 616 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human GO 110 Genes GS210006: GO:0044441 cilium part
Expand Tier I Mouse GO 4333 Genes GS184452: GO:0044422 organelle part
Expand Tier I Human 149 Genes GS172295: HP:0001513 Obesity
Expand Tier I Mouse GO 4073 Genes GS180034: GO:0032502 developmental process