Gene Details



INPP5E and homologs in 7 species are found in 886 GeneSets:


- Entrez   - GeneNetwork   - 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 1246 Genes GS165707: MP:0000428 abnormal craniofacial morphology
Expand Tier I Mouse GO 7755 Genes GS185131: GO:0044699 single-organism process
Expand Tier I Human 144 Genes GS228967: MSigDB Geneset - MORF_TPR
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 249 Genes GS205884: GO:0016311 dephosphorylation
Expand Tier II Human 10505 Genes GS238504: [MeSH] Tissues : D014024
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier II Human 5416 Genes GS237717: [MeSH] Tissue Distribution : D014018
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 II Human 14353 Genes GS244882: [MeSH] Epithelial Cells : D004847
Expand Tier II Human 8563 Genes GS234210: [MeSH] HeLa Cells : D006367
Expand Tier I Mouse GO 1822 Genes GS190997: GO:0044281 small molecule metabolic process
Expand Tier I Mouse MP 3520 Genes GS169830: MP:0005384 cellular phenotype
Expand Tier II Human 1164 Genes GS237543: [MeSH] Glycerophospholipids : D020404
Expand Tier I Human 267 Genes GS172261: HP:0000357 Abnormal location of ears
Expand Tier I Human 5 Genes GS172633: HP:0002871 Central apnea
Expand Tier II Human 11812 Genes GS236947: [MeSH] Brain : D001921
Expand Tier I Human 840 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier II Human 70216 Genes GS235234: [MeSH] Biochemical Phenomena : D001669
Expand Tier I Mouse 199 Genes GS229492: MSigDB Geneset - GSE17721_POLYIC_VS_PAM3CSK4_2H_BMDM_UP
Expand Tier I Human CTD 200 Genes GS125369: Lamivudine interacting genes (MeSH:D019259) in CTD
Expand Tier II Human 31959 Genes GS237114: [MeSH] Regulatory Elements, Transcriptional : D050436
Expand Tier I Mouse MP 328 Genes GS165382: MP:0001260 increased body weight
Expand Tier I Mouse MP 190 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 417 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 508 Genes GS167046: MP:0003881 abnormal nephron morphology
Expand Tier II Human 4661 Genes GS238716: [MeSH] Genetic Linkage : D008040
Expand Tier I Human 17 Genes GS172643: HP:0002365 Hypoplasia of the brainstem
Expand Tier III Rat 364 Genes GS223210: Gastric cancer resistance QTL 2 (Gcr2 Published QTL Chr 3)
Expand Tier I Mouse MP 368 Genes GS166406: MP:0002110 abnormal digit morphology
Expand Tier I Human 70 Genes GS175439: HP:0009136 Duplication involving bones of the feet
Expand Tier II Human 15702 Genes GS245264: [MeSH] Nervous System : D009420
Expand Tier I Human 178 Genes GS176151: HP:0000256 Macrocephaly
Expand Tier I Human 489 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Human 357 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Human 135 Genes GS170969: HP:0000157 Abnormality of the tongue
Expand Tier I Human 156 Genes GS172363: HP:0004324 Increased body weight
Expand Tier II Human 813 Genes GS236472: [MeSH] Phosphatidylinositols : D010716
Expand Tier II Mouse 61 Genes GS35675: Whole Brain Gene expression correlates of Morphine photocell counts minutes 75-90 in Males BXD
Expand Tier I Mouse MP 667 Genes GS170021: MP:0011087 complete neonatal lethality
Expand Tier I Human 782 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 237 Genes GS206874: GO:0006650 glycerophospholipid metabolic process
Expand Tier II Human 3455 Genes GS239907: [MeSH] Cell Surface Extensions : D022081
Expand Tier II Mouse 60 Genes GS36697: Whole Brain Gene expression correlates of Morphine Vertical Activity 30-45 min in Females BXD
Expand Tier II Mouse 40 Genes GS35705: Whole Brain Gene expression correlates of Morphine distance (cm) travelled minutes 105-120 in Males BXD
Expand Tier II Human 14581 Genes GS241611: [MeSH] Organic Chemistry Processes : D055602
Expand Tier I Human 423 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Mouse MP 121 Genes GS166938: MP:0002828 abnormal renal glomerular capsule morphology
Expand Tier I Human GO 441 Genes GS209602: GO:0051960 regulation of nervous system development
Expand Tier I Human 69 Genes GS172825: HP:0001829 Polydactyly (feet)
Expand Tier I Human 102 Genes GS229797: MSigDB Geneset - MORF_ERCC2
Expand Tier II Human 7025 Genes GS239838: [MeSH] Luminescent Proteins : D008164
Expand Tier I Mouse 543 Genes GS136612: colon tumor susceptibility 2 (Scc2, Published QTL Chr 2)
Expand Tier II Mouse 92 Genes GS35700: Whole Brain Gene expression correlates of Morphine distance (cm) travelled minutes 105-120 in Females BXD
Expand Human 195 Genes GS222320: Genes associated with high risk of intellectual disability.
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier II Human 2660 Genes GS244236: [MeSH] Homozygote : D006720
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 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Mouse GO 3615 Genes GS178359: GO:0071840 cellular component organization or biogenesis
Expand Tier II Mouse 62 Genes GS36702: Whole Brain Gene expression correlates of Morphine Vertical Activity 30-45 min in Males BXD
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 453 Genes GS84122: ethanol conditioned taste aversion (Published QTL, Chr 2)
Expand Tier I Mouse MP 619 Genes GS165194: MP:0001533 abnormal skeleton physiology
Expand Tier I Mouse MP 1246 Genes GS165228: MP:0005382 craniofacial phenotype
Expand Tier I Mouse MP 254 Genes GS170425: MP:0004508 abnormal pectoral girdle bone morphology
Expand Tier I Mouse MP 902 Genes GS164333: MP:0000516 abnormal renal/urinary system morphology
Expand Tier I Human 116 Genes GS172063: HP:0000107 Renal cysts
Expand Tier I Human 46 Genes GS172570: HP:0000341 Narrow forehead
Expand Tier I Human GO 1006 Genes GS196988: GO:0045595 regulation of cell differentiation
Expand Tier I Human GO 253 Genes GS195576: GO:0016791 phosphatase activity
Expand Tier II Human 9858 Genes GS242870: [MeSH] Polymorphism, Genetic : D011110
Expand Tier I Mouse GO 2762 Genes GS178357: GO:0071842 cellular component organization at cellular level
Expand Tier I Human 200 Genes GS176242: HP:0004207 Abnormality of the 5th finger
Expand Tier I Human GO 4338 Genes GS205500: GO:0071944 cell periphery
Expand Tier II Human 4022 Genes GS234926: [MeSH] Epithelium : D004848
Expand Tier I Human 454 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier II Human 12291 Genes GS238872: [MeSH] Central Nervous System : D002490
Expand Tier I Monkey 98 Genes GS233062: KEGG Geneset - "Phosphatidylinositol signaling system" pathway genes
Expand Tier I Mouse MP 2070 Genes GS163824: MP:0001259 abnormal body weight
Expand Tier I Human 5 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 17 Genes GS198911: GO:0046839 phospholipid dephosphorylation
Expand Tier I Human 122 Genes GS173242: HP:0001337 Tremor
Expand Tier I Mouse MP 323 Genes GS163432: MP:0006069 abnormal retinal neuronal layer morphology
Expand Tier III Rat 165 Genes GS224578: Estrogen-induced pituitary tumorigenesis QTL 17 (Ept17 Published QTL Chr 3)
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 67 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 Human 101 Genes GS175263: HP:0001161 Polydactyly (hands)
Expand Tier I Human 737 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 68 Genes GS176437: HP:0002334 Abnormality of the cerebellar vermis
Expand Tier I Human 260 Genes GS170933: HP:0001288 Gait disturbance
Expand Tier I Mouse GO 1209 Genes GS178284: GO:0031090 organelle membrane
Expand Tier II Human 56846 Genes GS235305: [MeSH] DNA, Complementary : D018076
Expand Tier II Human 24839 Genes GS237194: [MeSH] Physiological Phenomena : D010829
Expand Tier II Human 8660 Genes GS239079: [MeSH] Cell Membrane : D002462
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 1766 Genes GS194455: GO:0051239 regulation of multicellular organismal process
Expand Tier I Human 532 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human 18 Genes GS175110: HP:0000570 Abnormality of saccadic eye movements
Expand Tier I Human 178 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 395 Genes GS167615: MP:0003935 abnormal craniofacial development
Expand Tier II Human 67553 Genes GS240572: [MeSH] DNA : D004247
Expand Tier II Human 31495 Genes GS241930: [MeSH] Mutation : D009154
Expand Tier I Mouse GO 244 Genes GS179362: GO:0005929 cilium
Expand Tier I Human GO 1762 Genes GS196284: GO:0012505 endomembrane system
Expand Tier I Mouse GO 12 Genes GS184537: GO:0071545 inositol phosphate catabolic process
Expand Tier I Human 532 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 II Human 20510 Genes GS237794: [MeSH] Oligodeoxyribonucleotides : D009838
Expand Tier I Human 36 Genes GS174701: HP:0000556 Retinal dystrophy
Expand Tier I Human GO 3116 Genes GS197892: GO:0043228 non-membrane-bounded organelle
Expand Tier I Mouse MP 1052 Genes GS166409: MP:0002114 abnormal axial skeleton morphology
Expand Tier II Human 43280 Genes GS236911: [MeSH] Transcription, Genetic : D014158
Expand Tier II Human 65203 Genes GS235942: [MeSH] Genetic Processes : D039361
Expand Tier I Mouse GO 2565 Genes GS192299: GO:0006793 phosphorus metabolic process
Expand Tier I Human GO 1095 Genes GS208716: GO:2000026 regulation of multicellular organismal development
Expand Tier II Human 390 Genes GS237939: [MeSH] Chromosomes, Human, Pair 9 : D002899
Expand Tier II Human 253 Genes GS236399: [MeSH] Consanguinity : D003241
Expand Tier I Human 57 Genes GS230619: MSigDB Geneset - MORF_REV3L
Expand Tier II Human 14624 Genes GS236362: [MeSH] Organic Chemistry Phenomena : D055601
Expand Tier I Human GO 5623 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 177 Genes GS171047: HP:0008736 Hypoplasia of penis
Expand Tier I Human 153 Genes GS175880: HP:0007370 Aplasia/Hypoplasia of the corpus callosum
Expand Tier I Mouse MP 94 Genes GS167521: MP:0005306 abnormal phalanx morphology
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier I Human GO 699 Genes GS205439: GO:0031175 neuron projection development
Expand Tier I Human 199 Genes GS227831: MSigDB Geneset - V$HSF_Q6
Expand Tier II Human 79329 Genes GS243722: [MeSH] Genetic Structures : D040342
Expand Tier I Human GO 9155 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier III Mouse 6189 Genes GS213074: Genes with suggestive difference in (B6PF1) vs (PB6F1 + B6 + PWD) comparison
Expand Tier II Human 67130 Genes GS241889: [MeSH] Molecular Structure : D015394
Expand Tier III Mouse 7843 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 1317 Genes GS169832: MP:0005381 digestive/alimentary phenotype
Expand Tier I Human 248 Genes GS176844: HP:0000429 Abnormality of the nasal alae
Expand Tier I Human GO 2509 Genes GS207903: GO:0044281 small molecule metabolic process
Expand Tier I Human 833 Genes GS232630: PC Geneset - "Neuronal System" pathway genes
Expand Tier I Human 576 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human GO 9088 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human 1220 Genes GS233833: KEGG Geneset - "Metabolic pathways" pathway genes
Expand Tier I Human 280 Genes GS176231: HP:0010938 Abnormality of the external nose
Expand Tier I Human GO 547 Genes GS205302: GO:0000139 Golgi membrane
Expand Tier II Human 4790 Genes GS243290: [MeSH] Substrate Specificity : D013379
Expand Tier I Mouse MP 543 Genes GS170680: MP:0003744 abnormal orofacial morphology
Expand Tier I Human 60 Genes GS174300: HP:0000718 Aggressive behavior
Expand Tier II Human 59585 Genes GS234621: [MeSH] Chemical Actions and Uses : D020164
Expand Tier II Human 62071 Genes GS235061: [MeSH] Amino Acids, Peptides, and Proteins : D000602
Expand Tier I Human GO 11 Genes GS201341: GO:0071545 inositol phosphate catabolic process
Expand Tier II Mouse 432 Genes GS34243: Neocortex Gene expression correlates of Light-Dark Box Percentage time in light in Males BXD
Expand Tier II Human 219 Genes GS234888: [MeSH] Phosphatidylinositol 4,5-Diphosphate : D019269
Expand Tier I Human 17 Genes GS175676: HP:0007362 Aplasia/Hypoplasia of the brainstem
Expand Tier II Mouse 56 Genes GS35525: Whole Brain Gene expression correlates of Morphine photocell counts minutes 90-105 in Males BXD
Expand Tier I Human 401 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Mouse GO 2190 Genes GS191129: GO:0016787 hydrolase activity
Expand Tier I Mouse 469 Genes GS136890: voluntary alcohol consumption QTL 4 (Vacq4, Published QTL Chr 2)
Expand Tier I Human 825 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Mouse 200 Genes GS227197: MSigDB Geneset - GSE30083_SP3_VS_SP4_THYMOCYTE_DN
Expand Tier I Human 110 Genes GS172484: HP:0009997 Duplication of phalanx of hand
Expand Tier II Human 8099 Genes GS236751: [MeSH] Polymorphism, Single Nucleotide : D020641
Expand Tier I Mouse GO 639 Genes GS192628: GO:0048666 neuron development
Expand Tier II Human 1261 Genes GS243450: [MeSH] Virus Physiological Phenomena : D018406
Expand Tier II Human 47536 Genes GS236298: [MeSH] Gene Expression : D015870
Expand Tier I Mouse 200 Genes GS228446: MSigDB Geneset - GSE27786_LIN_NEG_VS_NEUTROPHIL_DN
Expand Tier I Mouse GO 786 Genes GS179519: GO:0012505 endomembrane system
Expand Tier I Mouse MP 779 Genes GS166118: MP:0002109 abnormal limb morphology
Expand Tier II Human 3287 Genes GS237404: [MeSH] Chromosomes, Human, 6-12 and X : D002906
Expand Tier I Human GO 4085 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Mouse MP 3522 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier I Rat 1275 Genes GS233121: KEGG Geneset - "Metabolic pathways" pathway genes
Expand Tier I Human 122 Genes GS171946: HP:0002269 Abnormality of neuronal migration
Expand Tier I Human 356 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Human 471 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier II Human 36279 Genes GS241850: [MeSH] Genetic Variation : D014644
Expand Tier I Mouse MP 378 Genes GS165361: MP:0004624 abnormal thoracic cage morphology
Expand Tier II Human 3296 Genes GS238113: [MeSH] Membrane Lipids : D008563
Expand Tier I Mouse GO 8386 Genes GS189751: GO:0050794 regulation of cellular process
Expand Tier II Human 38809 Genes GS236076: [MeSH] Protein Conformation : D011487
Expand Tier I Human 361 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human GO 1853 Genes GS209010: GO:1901575 organic substance catabolic process
Expand Tier I Mouse MP 400 Genes GS163318: MP:0000521 abnormal kidney cortex morphology
Expand Tier I Mouse 3092 Genes GS128575: Ethanol induced LORR Chr# 2
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 1068 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 20 Genes GS231759: PC Geneset - "1D-myo-inositol hexakisphosphate biosynthesis II (mammalian)" pathway genes
Expand Tier I Human 695 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 541 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 16 Genes GS173187: HP:0007772 Impaired smooth pursuit
Expand Tier I Mouse GO 781 Genes GS184010: GO:0030030 cell projection organization
Expand Tier II Mouse 418 Genes GS36029: Neocortex Gene expression correlates of Light-Dark Box Total seconds spent in dark compartment in Males BXD
Expand Tier I Human 2114 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 510 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 8578 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 239 Genes GS166294: MP:0011109 partial lethality throughout fetal growth and development
Expand Tier I Human GO 7717 Genes GS207616: GO:0016020 membrane
Expand Tier I Human 780 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 244 Genes GS228933: MSigDB Geneset - MORF_MT4
Expand Tier I Mouse GO 3614 Genes GS180229: GO:0005886 plasma membrane
Expand Tier I Human GO 1722 Genes GS198004: GO:0007399 nervous system development
Expand Tier II Mouse 56 Genes GS36677: Whole Brain Gene expression correlates of Morphine vertical activity counts minutes 15-30 in Females & Males BXD
Expand Tier I Monkey 1267 Genes GS232962: KEGG Geneset - "Metabolic pathways" pathway genes
Expand Tier II Human 1441 Genes GS244148: [MeSH] Phosphatidic Acids : D010712
Expand Tier I Mouse GO 1166 Genes GS191779: GO:2000026 regulation of multicellular organismal development
Expand Tier I Human 532 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier II Human 50108 Genes GS239769: [MeSH] Gene Library : D015723
Expand Tier I Mouse 338 Genes GS129163: proteoglycan induced spondylitis 2 (Pgis2 Published QTL Chr 2)
Expand Tier II Human 58105 Genes GS242107: [MeSH] Chemical Processes : D055599
Expand Tier II Human 32929 Genes GS243578: [MeSH] Reading Frames : D016364
Expand Tier I Mouse MP 3051 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 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human 72 Genes GS171658: HP:0000612 Iris coloboma
Expand Tier I Human GO 217 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 Human 29996 Genes GS237597: [MeSH] Cell Physiological Processes : D055648
Expand Tier I Human GO 3506 Genes GS193991: GO:0048731 system development
Expand Tier II Mouse 90 Genes GS35535: Whole Brain Gene expression correlates of Morphine photocell counts minutes 105-120 in Females BXD
Expand Tier I Human GO 473 Genes GS200117: GO:0051130 positive regulation of cellular component organization
Expand Tier I Human 1878 Genes GS232001: PC Geneset - "Transmembrane transport of small molecules" pathway genes
Expand Tier I Mouse GO 11 Genes GS190065: GO:0046855 inositol phosphate dephosphorylation
Expand Tier I Human 4 Genes GS175631: HP:0100951 Enlarged fossa interpeduncularis
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 285 Genes GS168654: MP:0000111 cleft palate
Expand Tier I Human 1021 Genes GS231597: PC Geneset - "Metabolic pathways" pathway genes
Expand Tier I Mouse GO 14 Genes GS193068: GO:0046174 polyol catabolic process
Expand Tier II Human 216 Genes GS242464: [MeSH] Gene Products, gag : D015683
Expand Tier I Mouse 200 Genes GS227774: MSigDB Geneset - GSE27786_LIN_NEG_VS_NKTCELL_DN
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 II Human 20421 Genes GS237820: [MeSH] DNA Primers : D017931
Expand Tier I Human 296 Genes GS174145: HP:0005918 Abnormality of phalanx of finger
Expand Tier I Human GO 237 Genes GS196129: GO:0005929 cilium
Expand Tier I Mouse MP 3761 Genes GS165527: MP:0005378 growth/size phenotype
Expand Tier II Human 23569 Genes GS235276: [MeSH] Signal Transduction : D015398
Expand Tier II Human 14819 Genes GS244426: [MeSH] Tumor Cells, Cultured : D014407
Expand Tier II Human 8645 Genes GS234354: [MeSH] Cytoskeletal Proteins : D003598
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 35 Genes GS171655: HP:0000611 Choroid coloboma
Expand Tier II Human 3244 Genes GS240069: [MeSH] Microtubule Proteins : D008868
Expand Tier I Mouse MP 27 Genes GS169385: MP:0004320 split sternum
Expand Tier I Mouse GO 229 Genes GS185770: GO:0006644 phospholipid metabolic process
Expand Tier III Rat 165 Genes GS223557: Estrogen-induced pituitary tumorigenesis QTL 6 (Ept6 Published QTL Chr 3)
Expand Tier II Mouse 92 Genes GS36722: Whole Brain Gene expression correlates of Morphine vertical activity counts minutes 60-75 in Females & Males BXD
Expand Tier I Human GO 316 Genes GS201237: GO:0046486 glycerolipid metabolic process
Expand Tier I Human GO 494 Genes GS200286: GO:0060284 regulation of cell development
Expand Tier I Human GO 636 Genes GS201839: GO:0044463 cell projection part
Expand Tier I Human GO 665 Genes GS205609: GO:0044431 Golgi apparatus part
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Human 199 Genes GS229107: MSigDB Geneset - GSE360_CTRL_VS_B_MALAYI_HIGH_DOSE_DC_DN
Expand Tier I Human GO 1994 Genes GS207862: GO:0009056 catabolic process
Expand Tier I Human 2477 Genes GS231582: PC Geneset - "Signaling Pathways" pathway genes
Expand Tier I Mouse 542 Genes GS136087: lean body mass 1 (Lbm1, Published QTL Chr 2)
Expand Tier II Human 11815 Genes GS238961: [MeSH] Nerve Tissue Proteins : D009419
Expand Tier II Human 279 Genes GS239193: [MeSH] Polyproteins : D020815
Expand Tier II Human 18755 Genes GS242691: [MeSH] Embryonic Structures : D004628
Expand Tier I Mouse GO 2872 Genes GS178360: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier II Human 58261 Genes GS239502: [MeSH] Nucleic Acid Probes : D015341
Expand Tier I Human 199 Genes GS176660: HP:0000050 Hypoplastic genitalia
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier II Human 30111 Genes GS244835: [MeSH] Chromosomes : D002875
Expand Tier I Human GO 519 Genes GS198012: GO:0046434 organophosphate catabolic process
Expand Tier II Mouse 91 Genes GS35685: Whole Brain Gene expression correlates of Morphine distance (cm) travelled minutes 90-105 in Females BXD
Expand Tier I Human 139 Genes GS230425: MSigDB Geneset - MORF_RAP1A
Expand Tier I Human 604 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human GO 2361 Genes GS195036: GO:0031090 organelle membrane
Expand Tier I Human 219 Genes GS172288: HP:0000358 Posteriorly rotated ears
Expand Tier I Human 98 Genes GS233867: KEGG Geneset - "Phosphatidylinositol signaling system" pathway genes
Expand Tier I Mouse MP 54 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 1257 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 313 Genes GS176568: HP:0000486 Strabismus
Expand Tier II Human 73996 Genes GS244482: [MeSH] Nucleic Acids, Nucleotides, and Nucleosides : D009706
Expand Tier I Human 469 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 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 28 Genes GS173311: HP:0010651 Abnormality of the meninges
Expand Tier II Human 58105 Genes GS235797: [MeSH] DNA Probes : D015342
Expand Tier II Human 29719 Genes GS237296: [MeSH] RNA, Antisense : D016372
Expand Tier I Mouse MP 121 Genes GS167974: MP:0009653 abnormal palate development
Expand Tier II Mouse 468 Genes GS84124: ethanol consumption (Published QTL, Chr 2)
Expand Tier I Mouse GO 7644 Genes GS188399: GO:0044238 primary metabolic process
Expand Tier I Human 386 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Human 511 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human GO 7650 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier II Mouse 56 Genes GS36712: Whole Brain Gene expression correlates of Morphine vertical activity counts minutes 45-60 in Females BXD
Expand Tier II Human 52588 Genes GS245685: [MeSH] RNA : D012313
Expand Tier I Human 75 Genes GS172219: HP:0010301 Spinal dysraphism
Expand Tier I Human GO 71 Genes GS195616: GO:0032580 Golgi cisterna membrane
Expand Tier I Mouse 550 Genes GS136074: insulin QTL 7 (Insq7, Published QTL Chr 2)
Expand Tier II Human 1210 Genes GS235850: [MeSH] Virus Physiological Processes : D055681
Expand Tier III Rat 474 Genes GS224899: Alcohol consumption QTL 8 (Alc8 Published QTL Chr 3)
Expand Tier I Human GO 259 Genes GS202414: GO:0044712 single-organism catabolic process
Expand Tier II Human 307 Genes GS239709: [MeSH] Culture Media, Serum-Free : D016895
Expand Tier I Mouse MP 20 Genes GS163832: MP:0011065 abnormal kidney epithelial cell primary cilium morphology
Expand Tier I Human 140 Genes GS228394: MSigDB Geneset - MORF_CDC2L5
Expand Tier II Human 20860 Genes GS239302: [MeSH] Oligonucleotides : D009841
Expand Tier I Human GO 3402 Genes GS195113: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier III Mouse 2256 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 1376 Genes GS164261: MP:0002081 perinatal lethality
Expand Tier I Human 72 Genes GS176835: HP:0000426 Prominent nasal bridge
Expand Tier I Human 262 Genes GS229002: MSigDB Geneset - MORF_BRCA1
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 1454 Genes GS205144: GO:0048468 cell development
Expand Tier II Human 3263 Genes GS237180: [MeSH] Genetic Markers : D005819
Expand Tier I Human 64 Genes GS174379: HP:0002084 Encephalocele
Expand Tier II Mouse 72 Genes GS33992: Whole Brain Gene expression correlates of Morphine distance (cm) travelled minutes 75-90 in Females & Males BXD
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier II Human 13987 Genes GS237817: [MeSH] Cell Line, Tumor : D045744
Expand Tier I Human 260 Genes GS172033: HP:0000369 Low-set ears
Expand Tier I Human 442 Genes GS176801: HP:0001263 Global developmental delay
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 II Human 28877 Genes GS238592: [MeSH] Cells, Cultured : D002478
Expand Tier II Human 423 Genes GS244985: [MeSH] Phosphatidylinositol Phosphates : D018129
Expand Tier I Mouse 97 Genes GS233407: KEGG Geneset - "Phosphatidylinositol signaling system" pathway genes
Expand Tier I Human 71 Genes GS233697: KEGG Geneset - "Inositol phosphate metabolism" pathway genes
Expand Tier I Human 81 Genes GS171773: HP:0000532 Chorioretinal abnormality
Expand Tier I Human 411 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 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Mouse MP 1562 Genes GS168149: MP:0005508 abnormal skeleton morphology
Expand Tier I Mouse GO 305 Genes GS189020: GO:0016311 dephosphorylation
Expand Tier I Mouse MP 2788 Genes GS167020: MP:0003956 abnormal body size
Expand Tier I Mouse MP 131 Genes GS169887: MP:0008272 abnormal endochondral bone ossification
Expand Tier I Mouse MP 317 Genes GS170380: MP:0003755 abnormal palate morphology
Expand Tier I Human 163 Genes GS176478: HP:0002119 Ventriculomegaly
Expand Tier I Mouse MP 77 Genes GS164164: MP:0009887 abnormal palatal shelf fusion at midline
Expand Tier II Mouse 102 Genes GS35515: Whole Brain Gene expression correlates of Morphine photocell counts minutes 90-105 in Females & Males BXD
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 550 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human 407 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human GO 258 Genes GS197043: GO:0044282 small molecule catabolic process
Expand Tier II Mouse 112 Genes GS36587: Whole Brain Gene expression correlates of Morphine vertical activity counts minutes 90-105 in Females & Males BXD
Expand Tier I Mouse 199 Genes GS228041: MSigDB Geneset - GSE2197_CPG_DNA_VS_UNTREATED_IN_DC_DN
Expand Tier I Human GO 1066 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 350 Genes GS198370: GO:0042578 phosphoric ester hydrolase activity
Expand Tier I Human 188 Genes GS228005: MSigDB Geneset - MORF_BNIP1
Expand Tier I Mouse MP 1674 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 288 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier I Mouse MP 179 Genes GS164411: MP:0000562 polydactyly
Expand Tier I Human 46 Genes GS173617: HP:0011220 Prominent forehead
Expand Tier I Human 1002 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 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier II Human 10133 Genes GS235960: [MeSH] Connective Tissue Cells : D003239
Expand Tier I Human 25 Genes GS232100: PC Geneset - "superpathway of D-myo-inositol (1,4,5)-trisphosphate metabolism" pathway genes
Expand Tier I Human 69 Genes GS232151: PC Geneset - "superpathway of inositol phosphate compounds" pathway genes
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 II Human 5185 Genes GS234976: [MeSH] Acylation : D000215
Expand Tier I Human CTD 377 Genes GS121976: Zidovudine interacting genes (MeSH:D015215) in CTD
Expand Tier I Mouse MP 2423 Genes GS168012: MP:0010832 lethality during fetal growth through weaning
Expand Tier I Human GO 2364 Genes GS207365: GO:0005829 cytosol
Expand Tier I Mouse 198 Genes GS229653: MSigDB Geneset - GSE9037_CTRL_VS_LPS_1H_STIM_BMDM_DN
Expand Tier I Human 375 Genes GS176038: HP:0002795 Functional respiratory abnormality
Expand Tier I Human 85 Genes GS229081: MSigDB Geneset - MORF_PTEN
Expand Tier II Human 305 Genes GS234923: [MeSH] Viral Core Proteins : D014758
Expand Tier I Human GO 9412 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 80 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 232 Genes GS202625: GO:0045017 glycerolipid biosynthetic process
Expand Tier I Human CTD 1151 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 II Human 58766 Genes GS243866: [MeSH] Laboratory Chemicals : D019995
Expand Tier I Human 209 Genes GS173206: HP:0003241 Genital hypoplasia
Expand Tier I Human 12202 Genes GS232685: PC Geneset - "Homo sapiens" pathway genes
Expand Tier I Mouse MP 60 Genes GS170285: MP:0004967 abnormal kidney epithelium morphology
Expand Tier I Human 936 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human 625 Genes GS232540: PC Geneset - "Amine compound SLC transporters" pathway genes
Expand Tier I Monkey 71 Genes GS233064: KEGG Geneset - "Inositol phosphate metabolism" pathway genes
Expand Tier I Human GO 731 Genes GS208043: GO:0016788 hydrolase activity, acting on ester bonds
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier II Human 338 Genes GS245473: [MeSH] Nucleocapsid Proteins : D019590
Expand Tier I Mouse MP 394 Genes GS165567: MP:0008271 abnormal bone ossification
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 11449 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Mouse GO 2538 Genes GS190893: GO:0030154 cell differentiation
Expand Tier I Human 211 Genes GS227356: MSigDB Geneset - MORF_ATRX
Expand Tier II Human 2037 Genes GS237303: [MeSH] Mutation, Missense : D020125
Expand Tier II Human 6867 Genes GS243608: [MeSH] Viral Proteins : D014764
Expand Tier II Human 58901 Genes GS243233: [MeSH] Specialty Uses of Chemicals : D020313
Expand Tier I Human GO 4250 Genes GS197009: GO:0005886 plasma membrane
Expand Tier I Human 2 Genes GS175455: HP:0002508 Malformation of brainstem structures
Expand Tier II Mouse 69 Genes GS36622: Whole Brain Gene expression correlates of Morphine vertical activity counts minutes 120-135 in Females BXD
Expand Tier I Human GO 6347 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human 521 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
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 192 Genes GS230228: MSigDB Geneset - GSE9006_HEALTHY_VS_TYPE_1_DIABETES_PBMC_1MONTH_POST_DX_DN
Expand Tier I Human 404 Genes GS173743: HP:0001999 Abnormal facial shape
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 468 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier I Human 242 Genes GS228700: MSigDB Geneset - V$NFAT_Q6
Expand Tier I Human GO 332 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 413 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier II Human 36882 Genes GS236241: [MeSH] Protein Structure, Tertiary : D017434
Expand Tier I Human GO 2816 Genes GS209411: GO:0048869 cellular developmental process
Expand Tier I Mouse GO 9 Genes GS178220: GO:0046030 inositol trisphosphate phosphatase activity
Expand Tier I Mouse GO 5879 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier II Mouse 72 Genes GS36692: Whole Brain Gene expression correlates of Morphine Vertical Activity 30-45 min in Females & Males BXD
Expand Tier I Human 81 Genes GS229511: MSigDB Geneset - MORF_HEAB
Expand Tier I Mouse GO 3605 Genes GS190682: GO:0007275 multicellular organismal development
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 886 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 407 Genes GS175670: HP:0007364 Aplasia/Hypoplasia of the cerebrum
Expand Tier I Mouse GO 1681 Genes GS191954: GO:0005856 cytoskeleton
Expand Tier I Human 209 Genes GS175990: HP:0000463 Anteverted nares
Expand Tier I Mouse 537 Genes GS136515: plasma plant sterol 2a (Plast2a, Published QTL Chr 2)
Expand Tier I Human GO 3300 Genes GS195110: GO:0071842 cellular component organization at cellular level
Expand Tier I Human 1261 Genes GS231784: PC Geneset - "Developmental Biology" pathway genes
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 259 Genes GS176172: HP:0001251 Ataxia
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse GO 18 Genes GS182118: GO:0046839 phospholipid dephosphorylation
Expand Tier III Rat 459 Genes GS223426: Blood pressure QTL 15 (Bp15 Published QTL Chr 3)
Expand Tier I Human 46 Genes GS170961: HP:0000158 Macroglossia
Expand Tier I Human 57 Genes GS232450: PC Geneset - "Inositol phosphate metabolism" pathway genes
Expand Tier I Mouse GO 8 Genes GS188388: GO:0034595 phosphatidylinositol phosphate 5-phosphatase activity
Expand Tier I Human 1055 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 52 Genes GS36727: Whole Brain Gene expression correlates of Morphine vertical activity counts minutes 60-75 in Females BXD
Expand Tier I Human GO 985 Genes GS204095: GO:0030182 neuron differentiation
Expand Tier I Mouse GO 980 Genes GS188826: GO:0022008 neurogenesis
Expand Tier II Human 8998 Genes GS240602: [MeSH] Biological Markers : D015415
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Mouse MP 944 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 II Mouse 99 Genes GS35545: Whole Brain Gene expression correlates of Morphine photocell counts minutes 120-135 in Females & Males BXD
Expand Tier I Mouse 459 Genes GS136228: mandible length 2 (Manln2, Published QTL Chr 2)
Expand Tier I Human 401 Genes GS229986: MSigDB Geneset - MORF_FOSL1
Expand Tier I Human GO 3116 Genes GS199272: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier I Mouse 70 Genes GS233500: KEGG Geneset - "Inositol phosphate metabolism" pathway genes
Expand Tier I Mouse MP 918 Genes GS165427: MP:0000432 abnormal head morphology
Expand Tier I Human 113 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 525 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human GO 22 Genes GS206952: GO:0046854 phosphatidylinositol phosphorylation
Expand Tier II Human 73356 Genes GS238415: [MeSH] Genome Components : D040481
Expand Tier I Human 837 Genes