Gene Details



TMEM216 and homologs in 3 species are found in 444 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 II Mouse 34 Genes GS34307: Hippocampus Gene expression correlates of Cue Conditioning - Activity suppression after 3rd tone/shock pairing in Males BXD
Expand Tier I Human 187 Genes GS171907: HP:0004299 Hernia of the abdominal wall
Expand Tier I Human 387 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Human GO 12 Genes GS203273: GO:0036038 TCTN-B9D complex
Expand Tier I Human 63 Genes GS175327: HP:0000568 Microphthalmos
Expand Tier I Human 271 Genes GS176826: HP:0000202 Oral cleft
Expand Tier I Human GO 675 Genes GS204996: GO:0048858 cell projection morphogenesis
Expand Tier I Human 38 Genes GS173462: HP:0001651 Dextrocardia
Expand Tier I Human 832 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 275 Genes GS170962: HP:0000159 Abnormality of the lip
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 537 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Tier I Human 282 Genes GS175900: HP:0009118 Aplasia/Hypoplasia of the mandible
Expand Tier I Mouse 645 Genes GS136227: mandible length 19 (Manln19, Published QTL Chr 19)
Expand Tier I Human 6 Genes GS174960: HP:0011932 Abnormality of the superior cerebellar peduncle
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Human 85 Genes GS173946: HP:0002438 Cerebellar malformation
Expand Tier I Human 50 Genes GS173113: HP:0002186 Apraxia
Expand Tier I Human 269 Genes GS172261: HP:0000357 Abnormal location of ears
Expand Tier I Human 156 Genes GS174002: HP:0000189 Narrow palate
Expand Tier I Human 5 Genes GS172633: HP:0002871 Central apnea
Expand Tier I Human 6 Genes GS175837: HP:0002419 Molar tooth sign on MRI
Expand Tier I Human 170 Genes GS174488: HP:0000525 Abnormality of the iris
Expand Tier I Human 845 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human 84 Genes GS175531: HP:0000003 Multicystic kidney dysplasia
Expand Tier I Human 129 Genes GS173247: HP:0007957 Reduction of corneal clarity
Expand Tier I Human 189 Genes GS176004: HP:0100656 Thoracoabdominal wall defects
Expand Tier I Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Human 17 Genes GS172643: HP:0002365 Hypoplasia of the brainstem
Expand Tier I Mouse 645 Genes GS135832: fluctuating asymmetry QTL 10 (Faq10, Published QTL Chr 19)
Expand Tier I Human 70 Genes GS175439: HP:0009136 Duplication involving bones of the feet
Expand Tier I Mouse 522 Genes GS136295: modifier of p53-deficiency 1 (Mp53d1, Published QTL Chr 19)
Expand Tier I Human 49 Genes GS173605: HP:0004426 Abnormality of the cheeks
Expand Tier I Human 178 Genes GS176151: HP:0000256 Macrocephaly
Expand Tier I Mouse 558 Genes GS136805: tibia bone quality traits 7 (Tbqt7, Published QTL Chr 19)
Expand Tier I Human 146 Genes GS170968: HP:0000156 High-arched palate
Expand Tier I Human 52 Genes GS171623: HP:0008055 Aplasia/Hypoplasia affecting the uvea
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 602 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Human 51 Genes GS175893: HP:0000932 Abnormality of the posterior cranial fossa
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 4024 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human 168 Genes GS170916: HP:0008056 Aplasia/Hypoplasia affecting the eye
Expand Tier I Mouse 440 Genes GS135479: bone response to mechanical loading 12 (Brml12, Published QTL Chr 19)
Expand Tier I Mouse 648 Genes GS136241: macrophage-associated risk inflammatory factor 3 (Marif3, Published QTL Chr 19)
Expand Tier I Human 533 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier I Human 786 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human GO 1287 Genes GS205610: GO:0044430 cytoskeletal part
Expand Tier I Human 264 Genes GS173014: HP:0010936 Abnormality of the lower urinary tract
Expand Tier I Mouse GO 5734 Genes GS190713: GO:0016021 integral to membrane
Expand Tier I Human 639 Genes GS172032: HP:0000366 Abnormality of the nose
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 490 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Human 13 Genes GS175255: HP:0010459 True hermaphroditism
Expand Tier I Mouse GO 1464 Genes GS182313: GO:0044085 cellular component biogenesis
Expand Tier I Human 426 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Human 324 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier I Human 13 Genes GS174063: HP:0100732 Pancreatic fibrosis
Expand Tier I Human 69 Genes GS172825: HP:0001829 Polydactyly (feet)
Expand Tier II Mouse 131 Genes GS36765: Hippocampus Gene expression correlates of Zero Maze - Percentage open time in Females & Males BXD
Expand Tier I Human GO 938 Genes GS210237: GO:0000902 cell morphogenesis
Expand Tier I Human GO 137 Genes GS194127: GO:0010927 cellular component assembly involved in morphogenesis
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 137 Genes GS175674: HP:0007360 Aplasia/Hypoplasia of the cerebellum
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
Expand Tier I Mouse GO 8406 Genes GS177404: GO:0005737 cytoplasm
Expand Tier I Mouse GO 3493 Genes GS177570: GO:0016043 cellular component organization
Expand Tier I Mouse GO 808 Genes GS192584: GO:0032989 cellular component morphogenesis
Expand Tier I Human GO 1789 Genes GS208893: GO:0005856 cytoskeleton
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Mouse GO 3615 Genes GS178359: GO:0071840 cellular component organization or biogenesis
Expand Tier I Mouse GO 3597 Genes GS188142: GO:0048856 anatomical structure development
Expand Tier I Human 303 Genes GS172416: HP:0002242 Abnormality of the intestine
Expand Tier I Human 66 Genes GS176263: HP:0100259 Postaxial polydactyly
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 486 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human 392 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Mouse GO 2762 Genes GS178357: GO:0071842 cellular component organization at cellular level
Expand Tier I Human 174 Genes GS171806: HP:0005656 Positional foot deformities
Expand Tier I Human 30 Genes GS174729: HP:0010322 Abnormality of the 5th toe
Expand Tier I Mouse 645 Genes GS135445: bone length and organs 11 (Bod11, Published QTL Chr 19)
Expand Tier I Human 202 Genes GS176242: HP:0004207 Abnormality of the 5th finger
Expand Tier I Human 237 Genes GS171395: HP:0000175 Cleft palate
Expand Tier II Mouse 685 Genes GS84316: alcohol preference locus (Published QTL, Chr 19)
Expand Tier I Human 545 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human 344 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human 215 Genes GS172139: HP:0010993 Abnormality of the cerebral subcortex
Expand Tier I Human 453 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Human 239 Genes GS174066: HP:0100737 Abnormality of the hard palate
Expand Tier I Human 737 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human 456 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Mouse 465 Genes GS136458: postnatal body weight growth 20 (Pbwg20, Published QTL Chr 19)
Expand Tier I Human 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
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 II Mouse 786 Genes GS84315: METH responses for body temperature (Published QTL, Chr 19)
Expand Tier I Human 159 Genes GS176900: HP:0000218 High palate
Expand Tier I Human 6 Genes GS172511: HP:0002335 Agenesis of cerebellar vermis
Expand Tier I Human 416 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier I Mouse GO 469 Genes GS188136: GO:0048858 cell projection morphogenesis
Expand Tier I Human GO 687 Genes GS197017: GO:0032990 cell part morphogenesis
Expand Tier I Human 89 Genes GS176824: HP:0000204 Cleft upper lip
Expand Tier I Human 348 Genes GS176615: HP:0000277 Abnormality of the mandible
Expand Tier I Human 123 Genes GS173242: HP:0001337 Tremor
Expand Tier II Mouse 685 Genes GS84317: alcohol preference locus (Published QTL, Chr 19)
Expand Tier I Human 4 Genes GS176837: HP:0002790 Neonatal breathing dysregulation
Expand Tier I Human 13 Genes GS172095: HP:0000588 Optic nerve coloboma
Expand Tier I Human 21 Genes GS171661: HP:0000617 Abnormality of ocular smooth pursuit
Expand Tier I Human 397 Genes GS173137: HP:0011821 Abnormality of facial skeleton
Expand Tier I Human 23 Genes GS171937: HP:0004346 Increased respiratory rate or depth of breathing
Expand Tier I Human 398 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Human 212 Genes GS176185: HP:0100790 Hernia
Expand Tier I Human 39 Genes GS175468: HP:0001177 Preaxial polydactyly (hands)
Expand Tier I Human 487 Genes GS171789: HP:0001392 Abnormality of the liver
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 II Mouse 22 Genes GS35900: Whole Brain Gene expression correlates of Number of entries into open arms of plus maze in Males BXD
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 Human 36 Genes GS172842: HP:0000480 Retinal coloboma
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human 19 Genes GS175110: HP:0000570 Abnormality of saccadic eye movements
Expand Tier I Human 44 Genes GS175961: HP:0000062 Ambiguous genitalia
Expand Tier I Human 46 Genes GS173882: HP:0001305 Dandy-Walker malformation
Expand Tier I Human 492 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Human 51 Genes GS171628: HP:0008053 Aplasia/Hypoplasia of the iris
Expand Tier I Human 51 Genes GS171787: HP:0001395 Hepatic fibrosis
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 179 Genes GS176589: HP:0001273 Abnormality of the corpus callosum
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 Human 281 Genes GS171204: HP:0011314 Abnormality of long bone morphology
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Mouse GO 244 Genes GS179362: GO:0005929 cilium
Expand Tier I Human 94 Genes GS174879: HP:0002104 Apnea
Expand Tier I Human 33 Genes GS173194: HP:0012090 Abnormality of pancreas morphology
Expand Tier I Human 47 Genes GS172604: HP:0005445 Widened posterior fossa
Expand Tier I Human 20 Genes GS172391: HP:0000221 Furrowed tongue
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 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 229 Genes GS171908: HP:0004298 Abnormality of the abdominal wall
Expand Tier I Human 30 Genes GS172587: HP:0001830 Postaxial polydactyly of foot
Expand Tier I Mouse GO 87 Genes GS190034: GO:0031513 nonmotile primary cilium
Expand Tier I Mouse GO 135 Genes GS177398: GO:0010927 cellular component assembly involved in morphogenesis
Expand Tier I Human 680 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human 67 Genes GS172844: HP:0000482 Microcornea
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Human 274 Genes GS172372: HP:0000648 Optic atrophy
Expand Tier I Human 154 Genes GS175880: HP:0007370 Aplasia/Hypoplasia of the corpus callosum
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier I Mouse GO 2876 Genes GS181102: GO:0043228 non-membrane-bounded organelle
Expand Tier II Mouse 119 Genes GS36775: Hippocampus Gene expression correlates of Zero Maze - Percentage open time in Males BXD
Expand Tier I Human 50 Genes GS174418: HP:0010950 Abnormality of the fourth ventricle
Expand Tier I Human 142 Genes GS171178: HP:0000238 Hydrocephalus
Expand Tier I Mouse GO 5859 Genes GS182404: GO:0031224 intrinsic to membrane
Expand Tier I Human 249 Genes GS176844: HP:0000429 Abnormality of the nasal alae
Expand Tier I Human GO 6278 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human 579 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human 599 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Human 281 Genes GS176231: HP:0010938 Abnormality of the external nose
Expand Tier I Human GO 2050 Genes GS203406: GO:0009653 anatomical structure morphogenesis
Expand Tier I Human 19 Genes GS174878: HP:0100957 Abnormality of the renal medulla
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 5320 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Human 28 Genes GS171678: HP:0002612 Congenital hepatic fibrosis
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human 75 Genes GS174446: HP:0001120 Abnormality of corneal size
Expand Tier I Human 41 Genes GS172019: HP:0001360 Holoprosencephaly
Expand Tier I Human 20 Genes GS173717: HP:0002323 Anencephaly
Expand Tier I Human 65 Genes GS174481: HP:0010576 Intracranial cystic lesion
Expand Tier I Human 17 Genes GS175676: HP:0007362 Aplasia/Hypoplasia of the brainstem
Expand Tier II Mouse 632 Genes GS84314: METH responses for body temperature (Published QTL, Chr 19)
Expand Tier I Human 232 Genes GS170999: HP:0000082 Abnormality of renal physiology
Expand Tier I Human 403 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Mouse GO 1466 Genes GS180001: GO:0048646 anatomical structure formation involved in morphogenesis
Expand Tier II Mouse 134 Genes GS36790: Hippocampus Gene expression correlates of Zero Maze - Time in Closed Arms in Males BXD
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier II Mouse 55 Genes GS36852: Whole Brain Gene expression correlates of Percentage of entries into closed arms of plus maze in Males BXD
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 I Human 110 Genes GS172484: HP:0009997 Duplication of phalanx of hand
Expand Tier I Mouse GO 6473 Genes GS184448: GO:0044425 membrane part
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 Human 258 Genes GS172272: HP:0001197 Abnormality of prenatal development or birth
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 16 Genes GS176249: HP:0002789 Tachypnea
Expand Tier I Human GO 863 Genes GS209634: GO:0015630 microtubule cytoskeleton
Expand Tier I Human GO 4097 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human 8 Genes GS173783: HP:0010297 Bifid tongue
Expand Tier I Human 246 Genes GS176806: HP:0003812 Phenotypic variability
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 Human GO 993 Genes GS209525: GO:0032989 cellular component morphogenesis
Expand Tier I Human 282 Genes GS172572: HP:0000347 Micrognathia
Expand Tier I Human 123 Genes GS171946: HP:0002269 Abnormality of neuronal migration
Expand Tier I Human GO 1126 Genes GS195108: GO:0071844 cellular component assembly at cellular level
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 II Mouse 88 Genes GS36098: Hippocampus Gene expression correlates of Baseline activity in fear conditioning apparatus in Females BXD
Expand Tier II Mouse 52 Genes GS35872: Striatum Gene expression correlates of Number of entries into closed arms of plus maze in Females & Males BXD
Expand Tier I Human 106 Genes GS171336: HP:0001732 Abnormality of the pancreas
Expand Tier I Human 58 Genes GS171822: HP:0000112 Nephropathy
Expand Tier II Mouse 134 Genes GS36805: Hippocampus Gene expression correlates of Zero Maze - total time in open quadrants in Males BXD
Expand Tier I Human GO 75 Genes GS198474: GO:0042384 cilium assembly
Expand Tier II Mouse 22 Genes GS36867: Whole Brain Gene expression correlates of Percentage of entries into open arms of plus maze in Males BXD
Expand Tier I Human 551 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human 337 Genes GS174076: HP:0009122 Aplasia/Hypoplasia affecting bones of the axial skeleton
Expand Tier I Human 364 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human 31 Genes GS172499: HP:0000037 Male pseudohermaphroditism
Expand Tier I Human 391 Genes GS175537: HP:0011277 Abnormality of the urinary system physiology
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier II Mouse 519 Genes GS84313: METH responses for body temperature (Published QTL, Chr 19)
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 426 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Human 699 Genes GS177031: HP:0011442 Abnormality of central motor function
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 I Human GO 1685 Genes GS199112: GO:0044085 cellular component biogenesis
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 Human 186 Genes GS171144: HP:0005280 Depressed nasal bridge
Expand Tier I Mouse 510 Genes GS135495: brain volume 2 (Brnvl2, Published QTL Chr 19)
Expand Tier I Human 228 Genes GS172470: HP:0001743 Abnormality of the spleen
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 Human 162 Genes GS175958: HP:0000795 Abnormality of the urethra
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 GO 7808 Genes GS207616: GO:0016020 membrane
Expand Tier I Human 780 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human 59 Genes GS171588: HP:0001562 Oligohydramnios
Expand Tier I Human 784 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 435 Genes GS175979: HP:0009115 Aplasia/Hypoplasia involving the skeleton
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 141 Genes GS174847: HP:0000940 Abnormal diaphysis morphology
Expand Tier I Human GO 110 Genes GS210006: GO:0044441 cilium part
Expand Tier II Mouse 27 Genes GS36857: Whole Brain Gene expression correlates of Percentage of entries into open arms of plus maze in Females & Males BXD
Expand Tier I Human 232 Genes GS173288: HP:0000316 Hypertelorism
Expand Tier I Mouse GO 4333 Genes GS184452: GO:0044422 organelle part
Expand Tier I Mouse GO 4073 Genes GS180034: GO:0032502 developmental process
Expand Tier I Human GO 4213 Genes GS195112: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human 543 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human 65 Genes GS176627: HP:0000457 Flat nose
Expand Tier I Human 534 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier I Mouse 645 Genes GS136687: skull morphology 26 (Skull26, Published QTL Chr 19)
Expand Tier I Human GO 66 Genes GS200476: GO:0005932 microtubule basal body
Expand Tier III Mouse 34 Genes GS34312: Hippocampus Gene expression correlates of Cue Conditioning - Activity suppression after 3rd tone/shock pairing [Basal Behavior] in Males BXD
Expand Tier I Human 72 Genes GS171658: HP:0000612 Iris coloboma
Expand Tier I Human 13 Genes GS171212: HP:0000090 Nephronophthisis
Expand Tier I Human 107 Genes GS172094: HP:0000589 Coloboma
Expand Tier I Human 61 Genes GS175264: HP:0001162 Postaxial polydactyly (hands)
Expand Tier I Mouse GO 609 Genes GS185024: GO:0044463 cell projection part
Expand Tier I Human 421 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human 302 Genes GS176029: HP:0009116 Aplasia/Hypoplasia involving bones of the skull
Expand Tier I Human 19 Genes GS172315: HP:0010295 Aplasia/Hypoplasia of the tongue
Expand Tier I Human 111 Genes GS173651: HP:0009142 Duplication of bones involving the upper extremities
Expand Tier I Mouse 522 Genes GS135752: experimental allergic encephalomyelitis susceptibility 19 (Eae19, Published QTL Chr 19)
Expand Tier I Human 4 Genes GS175631: HP:0100951 Enlarged fossa interpeduncularis
Expand Tier I Mouse 552 Genes GS135277: "alcohol preference locus 23, male specific" (Alcp23, Published QTL Chr 19)
Expand Tier I Human 311 Genes GS174899: HP:0100886 Abnormality of globe location
Expand Tier I Human 6 Genes GS173139: HP:0002418 Abnormality of the midbrain
Expand Tier I Human GO 930 Genes GS200809: GO:0030030 cell projection organization
Expand Tier I Human 346 Genes GS171309: HP:0000252 Microcephaly
Expand Tier II Mouse 148 Genes GS36795: Hippocampus Gene expression correlates of Zero Maze - total time in open quadrants in Females & Males BXD
Expand Tier I Human 298 Genes GS174145: HP:0005918 Abnormality of phalanx of finger
Expand Tier I Human 271 Genes GS174948: HP:0100763 Abnormality of the lymphatic system
Expand Tier I Human 416 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Human GO 238 Genes GS196129: GO:0005929 cilium
Expand Tier I Human 21 Genes GS172367: HP:0000647 Sclerocornea
Expand Tier I Human 198 Genes GS174236: HP:0000534 Abnormality of the eyebrow
Expand Tier I Mouse 645 Genes GS136430: pulmonary adenoma susceptibility 3 (Pas3, Published QTL Chr 19)
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Mouse GO 74 Genes GS193065: GO:0044441 cilium part
Expand Tier I Human 35 Genes GS171655: HP:0000611 Choroid coloboma
Expand Tier I Human 445 Genes GS175423: HP:0010461 Abnormality of the male genitalia
Expand Tier I Human 118 Genes GS172076: HP:0001163 Abnormality of the metacarpal bones
Expand Tier II Mouse 52 Genes GS36839: Striatum Gene expression correlates of Percentage of entries into closed arms of plus maze in Females & Males BXD
Expand Tier I Human 34 Genes GS172513: HP:0001696 Situs inversus totalis
Expand Tier I Human 4 Genes GS175402: HP:0002876 Tachypnea, episodic
Expand Tier I Mouse GO 197 Genes GS184011: GO:0030031 cell projection assembly
Expand Tier I Human GO 97 Genes GS198206: GO:0060271 cilium morphogenesis
Expand Tier I Human GO 637 Genes GS201839: GO:0044463 cell projection part
Expand Tier I Human 38 Genes GS174087: HP:0003363 Abdominal situs inversus
Expand Tier I Human 4 Genes GS173635: HP:0002404 Thickened superior cerebellar peduncle
Expand Tier I Human 358 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Human GO 16 Genes GS196524: GO:0035869 ciliary transition zone
Expand Tier I Human 64 Genes GS172899: HP:0011815 Cephalocele
Expand Tier I Mouse 552 Genes GS135278: "alcohol preference locus 24, female specific" (Alcp24, Published QTL Chr 19)
Expand Tier I Human 308 Genes GS172100: HP:0000587 Abnormality of the optic nerve
Expand Tier I Human GO 486 Genes GS208302: GO:0005815 microtubule organizing center
Expand Tier II Mouse 55 Genes GS34193: Whole Brain Gene expression correlates of Number of entries into closed arms of plus maze in Males BXD
Expand Tier I Human 397 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human 203 Genes GS174706: HP:0000553 Abnormality of the uvea
Expand Tier I Human 515 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Mouse GO 2991 Genes GS182469: GO:0043234 protein complex
Expand Tier I Human 115 Genes GS172148: HP:0010442 Polydactyly
Expand Tier I Mouse GO 2872 Genes GS178360: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Mouse GO 17 Genes GS179761: GO:0035869 ciliary transition zone
Expand Tier I Human 201 Genes GS176660: HP:0000050 Hypoplastic genitalia
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Mouse GO 1334 Genes GS178975: GO:0022607 cellular component assembly
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Human 236 Genes GS174257: HP:0000309 Abnormality of the midface
Expand Tier I Human 384 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 607 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human 38 Genes GS172855: HP:0004307 Abnormal anatomic location of the heart
Expand Tier I Human 49 Genes GS175305: HP:0000293 Full cheeks
Expand Tier I Human 221 Genes GS172288: HP:0000358 Posteriorly rotated ears
Expand Tier I Mouse GO 926 Genes GS178355: GO:0071844 cellular component assembly at cellular level
Expand Tier I Human 42 Genes GS172670: HP:0002363 Abnormality of the brainstem
Expand Tier I Human 990 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Human GO 1588 Genes GS196772: GO:0048646 anatomical structure formation involved in morphogenesis
Expand Tier I Human 47 Genes GS174712: HP:0002553 Highly arched eyebrow
Expand Tier I Human 63 Genes GS174833: HP:0006817 Aplasia/Hypoplasia of the cerebellar vermis
Expand Tier I Mouse GO 3583 Genes GS180236: GO:0032991 macromolecular complex
Expand Tier I Human 315 Genes GS176568: HP:0000486 Strabismus
Expand Tier I Mouse GO 482 Genes GS180237: GO:0032990 cell part morphogenesis
Expand Tier I Mouse GO 1850 Genes GS186562: GO:0009653 anatomical structure morphogenesis
Expand Tier I Mouse 440 Genes GS136111: long free running period 3 (Lfp3, Published QTL Chr 19)
Expand Tier I Human 474 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Mouse GO 102 Genes GS178598: GO:0072372 primary cilium
Expand Tier I Human GO 6151 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human 433 Genes GS172260: HP:0000356 Abnormality of the outer ear
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 172 Genes GS173476: HP:0002311 Incoordination
Expand Tier I Human 34 Genes GS172418: HP:0000567 Chorioretinal coloboma
Expand Tier II Mouse 49 Genes GS36038: Hippocampus Gene expression correlates of Light-Dark Box Total distance traveled in light and dark compartments in Females BXD
Expand Tier I Mouse GO 13 Genes GS186427: GO:0036038 TCTN-B9D complex
Expand Tier I Human GO 1224 Genes GS208482: GO:0042995 cell projection
Expand Tier I Human 388 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Mouse GO 747 Genes GS193294: GO:0000902 cell morphogenesis
Expand Tier I Human 567 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human 514 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier II Mouse 507 Genes GS84312: METH responses for body temperature (Published QTL, Chr 19)
Expand Tier I Human 56 Genes GS176885: HP:0002693 Abnormality of the skull base
Expand Tier I Human 126 Genes GS170894: HP:0006487 Bowing of the long bones
Expand Tier I Mouse GO 72 Genes GS181684: GO:0042384 cilium assembly
Expand Tier I Human GO 3409 Genes GS195113: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Human 72 Genes GS176835: HP:0000426 Prominent nasal bridge
Expand Tier I Human 140 Genes GS175471: HP:0001172 Abnormality of the thumb
Expand Tier I Human 64 Genes GS174379: HP:0002084 Encephalocele
Expand Tier II Mouse 27 Genes GS34202: Whole Brain Gene expression correlates of Number of entries into open arms of plus maze in Females & Males BXD
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Mouse 522 Genes GS136110: long free running period 2 (Lfp2, Published QTL Chr 19)
Expand Tier I Human 262 Genes GS172033: HP:0000369 Low-set ears
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 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 Human 19 Genes GS173221: HP:0006706 Cystic liver disease
Expand Tier I Human 71 Genes GS174898: HP:0100887 Abnormality of globe size
Expand Tier I Human GO 1544 Genes GS195733: GO:0022607 cellular component assembly
Expand Tier I Human 49 Genes GS176262: HP:0100258 Preaxial polydactyly
Expand Tier I Human 68 Genes GS176574: HP:0008062 Aplasia/Hypoplasia affecting the anterior segment of the eye
Expand Tier I Mouse GO 98 Genes GS181416: GO:0060271 cilium morphogenesis
Expand Tier I Human 163 Genes GS176478: HP:0002119 Ventriculomegaly
Expand Tier I Human GO 204 Genes GS200810: GO:0030031 cell projection assembly
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 Mouse 645 Genes GS135421: bitterness sensitivity 4 (Bits4, Published QTL Chr 19)
Expand Tier I Human 553 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human GO 5436 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Human 50 Genes GS171919: HP:0002198 Dilated fourth ventricle
Expand Tier I Human 189 Genes GS176745: HP:0010866 Abdominal wall defect
Expand Tier I Human GO 3861 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Human 34 Genes GS173140: HP:0011534 Abnormal spatial orientation of the cardiac segments
Expand Tier I Human 126 Genes GS175665: HP:0006504 Abnormality involving the diaphyses of the limbs
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 705 Genes GS136848: thymic lymphoma resistance 1 (Tlyr1, Published QTL Chr 19)
Expand Tier I Human GO 78 Genes GS206917: GO:0031513 nonmotile primary cilium
Expand Tier I Human 145 Genes GS171586: HP:0001560 Abnormality of the amniotic fluid
Expand Tier I Human 285 Genes GS175125: HP:0000028 Cryptorchidism
Expand Tier I Human 139 Genes GS171000: HP:0000083 Renal insufficiency
Expand Tier I Human 378 Genes GS176038: HP:0002795 Functional respiratory abnormality
Expand Tier I Human 47 Genes GS176066: HP:0002350 Cerebellar cyst
Expand Tier II Mouse 148 Genes GS36780: Hippocampus Gene expression correlates of Zero Maze - Time in Closed Arms in Females & Males BXD
Expand Tier I Human 139 Genes GS171397: HP:0000177 Abnormality of upper lip
Expand Tier I Human 81 Genes GS175635: HP:0002251 Aganglionic megacolon
Expand Tier I Human 70 Genes GS171543: HP:0000276 Long face
Expand Tier I Mouse 705 Genes GS136033: induction of brown adipocytes 4 (Iba4, Published QTL Chr 19)
Expand Tier I Human 211 Genes GS173206: HP:0003241 Genital hypoplasia
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 54 Genes GS172571: HP:0000340 Sloping forehead
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Mouse 471 Genes GS136359: nerve sheath tumor resistance QTL 1 (Nstr1, Published QTL Chr 19)
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 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 416 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier I Mouse 609 Genes GS135586: cholesterol absorption 5 (Chab5, Published QTL Chr 19)
Expand Tier I Human GO 2824 Genes GS209411: GO:0048869 cellular developmental process
Expand Tier I Human CTD 5075 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Tier II Mouse 111 Genes GS34908: Hippocampus Gene expression correlates of Open Field - Total distance traveled 0-5 minutes in Females BXD
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 Human 210 Genes GS175990: HP:0000463 Anteverted nares
Expand Tier I Mouse GO 1681 Genes GS191954: GO:0005856 cytoskeleton
Expand Tier I Human GO 3275 Genes GS199267: GO:0043234 protein complex
Expand Tier I Human 173 Genes GS175117: HP:0001883 Talipes
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 95 Genes GS195352: GO:0072372 primary cilium
Expand Tier I Human 5 Genes GS176393: HP:0011933 Elongated superior cerebellar peduncle
Expand Tier III Mouse 243 Genes GS35890: Whole Brain Gene expression correlates of Number of entries into open arms of plus maze [Ethanol] in Females & Males BXD
Expand Tier I Human 261 Genes GS176172: HP:0001251 Ataxia
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human GO 3125 Genes GS199272: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier I Human 15 Genes GS171339: HP:0001737 Pancreatic cysts
Expand Tier I Human 114 Genes GS173262: HP:0000864 Abnormality of the hypothalamus-pituitary axis
Expand Tier I Mouse 705 Genes GS136958: weight 6 (Wght6, Published QTL Chr 19)
Expand Tier I Human 529 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear