Gene Details



Whrn and homologs in 3 species are found in 480 GeneSets:


- Entrez   - Ensembl   - GeneNetwork   - STRING   - Allen Brain Atlas   - MGI   - 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 GO 7755 Genes GS185131: GO:0044699 single-organism process
Expand Tier I Mouse MP 519 Genes GS170662: MP:0000274 enlarged heart
Expand Tier I Mouse MP 182 Genes GS168433: MP:0002980 abnormal postural reflex
Expand Tier I Mouse 459 Genes GS129071: anticardiolipin antibody 2 (Acla2 Published QTL Chr 4)
Expand Tier I Mouse MP 50 Genes GS167803: MP:0005307 head tossing
Expand Tier I Mouse MP 215 Genes GS168129: MP:0010025 decreased total body fat amount
Expand Tier I Mouse 378 Genes GS136480: plasmacytoma susceptibility 2 (Pcyts2, Published QTL Chr 4)
Expand Tier II Mouse 21 Genes GS35363: Striatum Gene expression correlates of Amount of time in open arms of plus maze in Females & Males BXD
Expand Tier I Mouse 365 Genes GS135944: HDL QTL 10 (Hdlq10, Published QTL Chr 4)
Expand Tier I Human 154 Genes GS174979: HP:0011061 Abnormality of dental structure
Expand Tier I Mouse GO 454 Genes GS181012: GO:0007423 sensory organ development
Expand Tier I Mouse MP 184 Genes GS163581: MP:0001004 abnormal retinal photoreceptor morphology
Expand Tier I Human GO 13 Genes GS196948: GO:0060122 inner ear receptor stereocilium organization
Expand Tier I Mouse MP 192 Genes GS166394: MP:0003728 abnormal retinal photoreceptor layer morphology
Expand Tier I Mouse MP 469 Genes GS165308: MP:0004848 abnormal liver size
Expand Tier I Human GO 2507 Genes GS196934: GO:0065008 regulation of biological quality
Expand Tier I Human 379 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Mouse MP 49 Genes GS166022: MP:0004408 decreased cochlear hair cell number
Expand Tier I Human GO 124 Genes GS210482: GO:0007605 sensory perception of sound
Expand Tier I Mouse MP 69 Genes GS164014: MP:0001410 head bobbing
Expand Tier II Mouse 290 Genes GS83989: cocaine related behavior 5 (Cocrb5, Published QTL,Chr 4, MGI:2150991)
Expand Tier I Mouse MP 47 Genes GS164793: MP:0008587 short photoreceptor outer segment
Expand Tier I Human 141 Genes GS174906: HP:0000545 Myopia
Expand Tier I Mouse MP 2406 Genes GS166858: MP:0000685 abnormal immune system morphology
Expand Tier I Mouse MP 1290 Genes GS163965: MP:0011182 decreased hematopoietic cell number
Expand Tier I Mouse MP 1084 Genes GS166749: MP:0002221 abnormal lymph organ size
Expand Tier I Human GO 4 Genes GS198531: GO:0002139 stereocilia coupling link
Expand Tier I Human GO 20 Genes GS198334: GO:0001917 photoreceptor inner segment
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 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 16 Genes GS175180: HP:0011073 Abnormality of dental color
Expand Tier I Mouse MP 173 Genes GS168066: MP:0002622 abnormal cochlear hair cell morphology
Expand Tier I Mouse 357 Genes GS135446: bone length and organs 2 (Bod2, Published QTL Chr 4)
Expand Tier I Mouse MP 1008 Genes GS164333: MP:0000516 abnormal renal/urinary system morphology
Expand Tier I Mouse GO 2762 Genes GS178357: GO:0071842 cellular component organization at cellular level
Expand Tier II Mouse 139 Genes GS35465: Whole Brain Gene expression correlates of Difference in total distance traveled (cm) (saline-ethanol) in Males BXD
Expand Tier I Human 50 Genes GS173812: HP:0000738 Hallucinations
Expand Tier I Mouse MP 2357 Genes GS163824: MP:0001259 abnormal body weight
Expand Tier I Mouse GO 912 Genes GS179236: GO:0048699 generation of neurons
Expand Tier I Mouse MP 331 Genes GS163432: MP:0006069 abnormal retinal neuronal layer morphology
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 Mouse 365 Genes GS136230: mandible length 4 (Manln4, Published QTL Chr 4)
Expand Tier I Mouse MP 632 Genes GS170733: MP:0000188 abnormal circulating glucose level
Expand Tier I Human 124 Genes GS175492: HP:0000512 Abnormal electroretinogram
Expand Tier I Mouse GO 244 Genes GS179362: GO:0005929 cilium
Expand Tier I Mouse 297 Genes GS136495: proteoglycan induced arthritis 27 (Pgia27, Published QTL Chr 4)
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 384 Genes GS171708: HP:0000359 Abnormality of the inner ear
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Mouse 365 Genes GS136287: modifier of polycystic kidney disease progression 1 (Mopkd1, Published QTL Chr 4)
Expand Tier I Mouse MP 116 Genes GS168503: MP:0002059 abnormal seminal vesicle morphology
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier I Mouse 361 Genes GS135541: cerebellar cAMP 4 (Ccmp4, Published QTL Chr 4)
Expand Tier III Mouse 6105 Genes GS213074: Genes with suggestive difference in (B6PF1) vs (PB6F1 + B6 + PWD) comparison
Expand Tier I Mouse MP 990 Genes GS169075: MP:0002078 abnormal glucose homeostasis
Expand Tier I Mouse MP 1041 Genes GS168683: MP:0000598 abnormal liver morphology
Expand Tier I Human GO 93 Genes GS202123: GO:0030426 growth cone
Expand Tier I Mouse GO 639 Genes GS192628: GO:0048666 neuron development
Expand Tier I Mouse 299 Genes GS136700: systemic lupus erythmatosus susceptibility 2 (Sle2, Published QTL Chr 4)
Expand Tier I Human GO 4097 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Mouse 282 Genes GS136485: predicted fat percentage 1 (Pfat1, Published QTL Chr 4)
Expand Tier II Mouse 298 Genes GS84160: METH responses for climbing Ms6hm (Published QTL, Chr 4)
Expand Tier I Human 358 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Human 164 Genes GS174994: HP:0002059 Cerebral atrophy
Expand Tier I Human GO 39 Genes GS202686: GO:0060113 inner ear receptor cell differentiation
Expand Tier I Mouse MP 1420 Genes GS163052: MP:0000266 abnormal heart morphology
Expand Tier I Mouse 347 Genes GS129083: atherosclerosis 8 (Ath8 Published QTL Chr 4)
Expand Tier I Mouse GO 10879 Genes GS181473: GO:0005488 binding
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 Human GO 1724 Genes GS198004: GO:0007399 nervous system development
Expand Tier I Mouse MP 7 Genes GS167448: MP:0004536 short inner hair cell stereocilia
Expand Tier I Human GO 285 Genes GS202125: GO:0030424 axon
Expand Tier I Mouse 357 Genes GS135409: body growth late QTL 4 (Bglq4, Published QTL Chr 4)
Expand Tier I Mouse 459 Genes GS129177: splenomegaly-NZB x NZW 2 (Sbw2 Published QTL Chr 4)
Expand Tier I Mouse MP 3437 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Mouse MP 648 Genes GS164023: MP:0001961 abnormal reflex
Expand Tier I Mouse MP 73 Genes GS168793: MP:0005439 decreased glycogen level
Expand Tier I Mouse 362 Genes GS136775: synechia 1 (Synch1, Published QTL Chr 4)
Expand Tier I Mouse 311 Genes GS136247: metabolic syndrome (Mbsyd, Published QTL Chr 4)
Expand Tier I Mouse MP 57 Genes GS162960: MP:0003367 increased circulating glucocorticoid level
Expand Tier I Mouse MP 757 Genes GS163427: MP:0009205 abnormal internal male genitalia morphology
Expand Tier I Mouse MP 4173 Genes GS165527: MP:0005378 growth/size phenotype
Expand Tier I Human GO 154 Genes GS196917: GO:0048871 multicellular organismal homeostasis
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Mouse MP 466 Genes GS163138: MP:0005253 abnormal eye physiology
Expand Tier I Mouse MP 144 Genes GS164655: MP:0003068 enlarged kidney
Expand Tier I Mouse MP 71 Genes GS165854: MP:0004406 abnormal cochlear hair cell number
Expand Tier I Mouse GO 554 Genes GS188813: GO:0045202 synapse
Expand Tier I Mouse MP 55 Genes GS168880: MP:0004736 abnormal distortion product otoacoustic emission
Expand Tier I Human GO 488 Genes GS205674: GO:0045202 synapse
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Mouse MP 226 Genes GS169032: MP:0005551 abnormal eye electrophysiology
Expand Tier I Human 89 Genes GS173329: HP:0000682 Abnormality of dental enamel
Expand Tier I Human GO 8 Genes GS201149: GO:0001895 retina homeostasis
Expand Tier I Mouse GO 65 Genes GS187955: GO:0005902 microvillus
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Mouse MP 217 Genes GS166609: MP:0002833 increased heart weight
Expand Tier I Mouse GO 102 Genes GS178598: GO:0072372 primary cilium
Expand Tier I Mouse MP 1927 Genes GS168422: MP:0000716 abnormal immune system cell morphology
Expand Tier I Human GO 3409 Genes GS195113: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Mouse GO 133 Genes GS193043: GO:0050954 sensory perception of mechanical stimulus
Expand Tier I Human GO 1456 Genes GS205144: GO:0048468 cell development
Expand Tier I Mouse MP 1317 Genes GS166711: MP:0002160 abnormal reproductive system morphology
Expand Tier I Mouse MP 3110 Genes GS167020: MP:0003956 abnormal body size
Expand Tier I Mouse MP 2821 Genes GS169535: MP:0005397 hematopoietic system phenotype
Expand Tier I Human GO 1067 Genes GS196002: GO:0048699 generation of neurons
Expand Tier I Mouse 3096 Genes GS127928: Lateral septal complex - Allen Mouse Brain Atlas
Expand Tier I Human GO 3861 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Mouse MP 91 Genes GS162961: MP:0003366 abnormal circulating glucocorticoid level
Expand Tier I Human GO 78 Genes GS206917: GO:0031513 nonmotile primary cilium
Expand Tier I Mouse MP 438 Genes GS165390: MP:0003224 neuron degeneration
Expand Tier III Mouse 8107 Genes GS213076: Genes with suggestive difference in (B6) vs (B6PF1 + PB6F1 + PWD) comparison
Expand Tier I Mouse MP 826 Genes GS167323: MP:0003949 abnormal circulating lipid level
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human 93 Genes GS176289: HP:0002120 Cerebral cortical atrophy
Expand Tier I Mouse GO 2538 Genes GS190893: GO:0030154 cell differentiation
Expand Tier I Human 50 Genes GS173561: HP:0000691 Microdontia
Expand Tier I Mouse GO 323 Genes GS188368: GO:0015629 actin cytoskeleton
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Tier I Mouse MP 78 Genes GS166952: MP:0001157 small seminal vesicle
Expand Tier I Mouse MP 68 Genes GS165873: MP:0004404 cochlear outer hair cell degeneration
Expand Tier I Mouse GO 119 Genes GS193537: GO:0007605 sensory perception of sound
Expand Tier I Human GO 7336 Genes GS201431: GO:0005515 protein binding
Expand Tier I Mouse MP 72 Genes GS167784: MP:0002637 small uterus
Expand Tier I Mouse MP 2404 Genes GS165615: MP:0002123 abnormal hematopoiesis
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 5879 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 364 Genes GS205224: GO:0015629 actin cytoskeleton
Expand Tier I Mouse MP 17 Genes GS165666: MP:0004523 decreased cochlear hair cell stereocilia number
Expand Tier I Human GO 3275 Genes GS199267: GO:0043234 protein complex
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 189 Genes GS174247: HP:0000539 Abnormality of refraction
Expand Tier I Mouse 361 Genes GS135888: free running period 1 (Frp1, Published QTL Chr 4)
Expand Tier I Mouse MP 113 Genes GS168215: MP:0001967 deafness
Expand Tier I Mouse MP 3815 Genes GS169827: MP:0005387 immune system phenotype
Expand Tier I Mouse MP 1034 Genes GS163853: MP:0001547 abnormal lipid level
Expand Tier I Human GO 986 Genes GS204095: GO:0030182 neuron differentiation
Expand Tier I Human GO 3125 Genes GS199272: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier I Human GO 355 Genes GS202124: GO:0030425 dendrite
Expand Tier I Mouse 280 Genes GS135546: CD4 T cell subset 2 (Cd4ts2, Published QTL Chr 4)
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Mouse GO 6204 Genes GS184629: GO:0005515 protein binding
Expand Tier I Mouse 357 Genes GS136262: modifier of mammary tumor growth 1 (Mmtg1, Published QTL Chr 4)
Expand Tier I Mouse MP 181 Genes GS163498: MP:0003308 abnormal cochlear sensory epithelium morphology
Expand Tier I Mouse MP 642 Genes GS170236: MP:0005452 abnormal adipose tissue amount
Expand Tier I Mouse MP 466 Genes GS167324: MP:0003948 abnormal gas homeostasis
Expand Tier I Mouse MP 295 Genes GS169967: MP:0001408 stereotypic behavior
Expand Tier I Mouse MP 197 Genes GS166632: MP:0001120 abnormal uterus morphology
Expand Tier I Mouse MP 677 Genes GS165538: MP:0005377 hearing/vestibular/ear phenotype
Expand Tier I Mouse MP 574 Genes GS166743: MP:0002229 neurodegeneration
Expand Tier I Mouse GO 2279 Genes GS186488: GO:0048513 organ development
Expand Tier I Mouse MP 380 Genes GS163569: MP:0002557 abnormal social/conspecific interaction
Expand Tier I Mouse 282 Genes GS136923: viral myocarditis susceptibility locus 3 (Vms3, Published QTL Chr 4)
Expand Tier I Mouse MP 3543 Genes GS169095: MP:0004924 abnormal behavior
Expand Tier I Mouse MP 400 Genes GS164570: MP:0003878 abnormal ear physiology
Expand Tier I Mouse MP 54 Genes GS167164: MP:0004527 abnormal outer hair cell stereociliary bundle morphology
Expand Tier I Mouse MP 90 Genes GS170245: MP:0004022 abnormal cone electrophysiology
Expand Tier I Human GO 4567 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Mouse GO 1398 Genes GS181215: GO:0007399 nervous system development
Expand Tier I Mouse MP 455 Genes GS165816: MP:0001119 abnormal female reproductive system morphology
Expand Tier I Mouse MP 1914 Genes GS164022: MP:0008246 abnormal leukocyte morphology
Expand Tier I Mouse GO 15 Genes GS180171: GO:0060122 inner ear receptor stereocilium organization
Expand Tier I Mouse MP 574 Genes GS167217: MP:0001325 abnormal retina morphology
Expand Tier I Mouse GO 2876 Genes GS181102: GO:0043228 non-membrane-bounded organelle
Expand Tier I Mouse MP 142 Genes GS167107: MP:0005288 abnormal oxygen consumption
Expand Tier I Mouse MP 140 Genes GS169804: MP:0003731 abnormal retinal outer nuclear layer morphology
Expand Tier I Human GO 183 Genes GS204087: GO:0043583 ear development
Expand Tier I Mouse MP 56 Genes GS164345: MP:0006336 abnormal otoacoustic response
Expand Tier I Mouse GO 406 Genes GS182368: GO:0043025 neuronal cell body
Expand Tier II Mouse 106 Genes GS34754: Cerebellum Gene expression correlates of Novel environment vertical activity counts min 0-15 in Males BXD
Expand Tier I Mouse MP 779 Genes GS167267: MP:0001145 abnormal male reproductive system morphology
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Mouse MP 1130 Genes GS163227: MP:0003313 abnormal locomotor activation
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human 202 Genes GS171631: HP:0008051 Abnormality of the retinal pigment epithelium
Expand Tier I Human 344 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Mouse GO 43 Genes GS181742: GO:0043198 dendritic shaft
Expand Tier I Human GO 95 Genes GS202122: GO:0030427 site of polarized growth
Expand Tier I Mouse MP 72 Genes GS165663: MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology
Expand Tier I Mouse GO 2710 Genes GS192471: GO:0048869 cellular developmental process
Expand Tier I Mouse MP 92 Genes GS170195: MP:0008515 thin retinal outer nuclear layer
Expand Tier I Mouse MP 585 Genes GS165985: MP:0000965 abnormal sensory neuron morphology
Expand Tier I Mouse MP 647 Genes GS164446: MP:0005195 abnormal posterior eye segment morphology
Expand Tier I Mouse MP 487 Genes GS167105: MP:0008948 decreased neuron number
Expand Tier I Human GO 33 Genes GS198533: GO:0043198 dendritic shaft
Expand Tier I Mouse MP 211 Genes GS165114: MP:0004426 abnormal cochlear labyrinth morphology
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Mouse MP 153 Genes GS165530: MP:0001386 abnormal maternal nurturing
Expand Tier I Mouse 361 Genes GS136116: body length 3 (Lgth3, Published QTL Chr 4)
Expand Tier I Mouse MP 24 Genes GS165758: MP:0000642 enlarged adrenal glands
Expand Tier I Mouse MP 58 Genes GS168525: MP:0004908 abnormal seminal vesicle weight
Expand Tier I Mouse MP 114 Genes GS164970: MP:0000639 abnormal adrenal gland morphology
Expand Tier I Mouse MP 106 Genes GS166716: MP:0003729 abnormal photoreceptor outer segment morphology
Expand Tier I Mouse GO 49 Genes GS185850: GO:0060113 inner ear receptor cell differentiation
Expand Tier I Mouse MP 87 Genes GS165544: MP:0004362 cochlear hair cell degeneration
Expand Tier I Mouse GO 53 Genes GS180227: GO:0005884 actin filament
Expand Tier II Mouse 377 Genes GS84156: METH responses for body temperature (Published QTL, Chr 4)
Expand Tier I Mouse MP 1013 Genes GS164724: MP:0001516 abnormal motor coordination/ balance
Expand Tier I Mouse GO 26 Genes GS181543: GO:0001917 photoreceptor inner segment
Expand Tier I Human GO 45 Genes GS205662: GO:0042490 mechanoreceptor differentiation
Expand Tier I Mouse MP 1476 Genes GS169531: MP:0005391 vision/eye phenotype
Expand Tier I Mouse MP 833 Genes GS163103: MP:0000003 abnormal adipose tissue morphology
Expand Tier I Mouse MP 140 Genes GS169625: MP:0005437 abnormal glycogen level
Expand Tier I Human GO 4 Genes GS199423: GO:0002142 stereocilia ankle link complex
Expand Tier I Mouse MP 206 Genes GS165391: MP:0000972 abnormal mechanoreceptor morphology
Expand Tier I Human 472 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Mouse 364 Genes GS136239: macrophage-associated risk inflammatory factor 1 (Marif1, Published QTL Chr 4)
Expand Tier I Mouse 543 Genes GS129184: skin tumor susceptibility in FVB and PWK 1 (Skts-fp1 Published QTL Chr 4)
Expand Tier I Mouse MP 940 Genes GS165876: MP:0002135 abnormal kidney morphology
Expand Tier I Mouse MP 1825 Genes GS168956: MP:0003491 abnormal voluntary movement
Expand Tier I Mouse MP 159 Genes GS169054: MP:0005438 abnormal glycogen homeostasis
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 Mouse GO 1394 Genes GS191552: GO:0042995 cell projection
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse MP 3924 Genes GS163934: MP:0001764 abnormal homeostasis
Expand Tier I Mouse GO 4333 Genes GS184452: GO:0044422 organelle part
Expand Tier I Human GO 27 Genes GS198431: GO:0032421 stereocilium bundle
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 Mouse GO 444 Genes GS189435: GO:0044297 cell body
Expand Tier I Mouse 459 Genes GS129191: seizure susceptibility 2 (Szs2 Published QTL Chr 4)
Expand Tier I Mouse MP 102 Genes GS168517: MP:0004902 abnormal uterus size
Expand Tier I Human 381 Genes GS175714: HP:0011389 Functional abnormality of the inner ear
Expand Tier I Human GO 191 Genes GS207776: GO:0060249 anatomical structure homeostasis
Expand Tier I Mouse MP 249 Genes GS163316: MP:0000035 abnormal membranous labyrinth morphology
Expand Tier I Mouse MP 845 Genes GS165539: MP:0005375 adipose tissue phenotype
Expand Tier II Mouse 171 Genes GS26116: Positional candidate genes for Thermal Nociception Hargreaves' Test [Pain] in Females & Males for Suggestive BXD QTL on Chr4 from 44 to 64 Mb
Expand Tier I Human GO 157 Genes GS196324: GO:0048839 inner ear development
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 649 Genes GS207805: GO:0043005 neuron projection
Expand Tier I Human GO 930 Genes GS200809: GO:0030030 cell projection organization
Expand Tier I Human 188 Genes GS171512: HP:0007703 Abnormal retinal pigmentation
Expand Tier I Human 416 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Mouse 365 Genes GS135936: HDL level 36 (Hdl36, Published QTL Chr 4)
Expand Tier I Mouse MP 229 Genes GS170701: MP:0004847 abnormal liver weight
Expand Tier I Human GO 4 Genes GS199415: GO:0002141 stereocilia ankle link
Expand Tier I Human 368 Genes GS170971: HP:0000407 Sensorineural hearing impairment
Expand Tier I Mouse MP 209 Genes GS167140: MP:0003169 abnormal scala media morphology
Expand Tier I Mouse MP 145 Genes GS168434: MP:0002981 increased liver weight
Expand Tier I Mouse MP 174 Genes GS165804: MP:0002862 altered righting response
Expand Tier I Mouse MP 96 Genes GS164692: MP:0004021 abnormal rod electrophysiology
Expand Tier I Human GO 1136 Genes GS205691: GO:0022008 neurogenesis
Expand Tier I Mouse 369 Genes GS136585: rapid eye movement sleep 1 (Remslp1, Published QTL Chr 4)
Expand Tier I Mouse 357 Genes GS136237: mandible size 3 (Manz3, Published QTL Chr 4)
Expand Tier I Human 515 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Mouse GO 18 Genes GS181644: GO:0032420 stereocilium
Expand Tier I Mouse MP 875 Genes GS164301: MP:0005418 abnormal circulating hormone level
Expand Tier I Mouse GO 2991 Genes GS182469: GO:0043234 protein complex
Expand Tier I Mouse MP 164 Genes GS163724: MP:0000436 abnormal head movements
Expand Tier I Mouse MP 1316 Genes GS165798: MP:0005367 renal/urinary system phenotype
Expand Tier I Mouse GO 1140 Genes GS188751: GO:0044430 cytoskeletal part
Expand Tier I Mouse GO 55 Genes GS188801: GO:0042490 mechanoreceptor differentiation
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Mouse MP 2663 Genes GS168995: MP:0009642 abnormal blood homeostasis
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Mouse GO 1378 Genes GS188287: GO:0048468 cell development
Expand Tier II Mouse 423 Genes GS36580: Hippocampus Gene expression correlates of Novel Open Field Number of urinations in Males BXD
Expand Tier I Mouse MP 2644 Genes GS169829: MP:0005385 cardiovascular system phenotype
Expand Tier I Mouse GO 3583 Genes GS180236: GO:0032991 macromolecular complex
Expand Tier I Mouse 359 Genes GS136067: immune response to AAV2 QTL 1 (Imraq1, Published QTL Chr 4)
Expand Tier I Human 172 Genes GS173476: HP:0002311 Incoordination
Expand Tier I Mouse MP 90 Genes GS166300: MP:0005345 abnormal circulating corticosterone level
Expand Tier I Human GO 1224 Genes GS208482: GO:0042995 cell projection
Expand Tier I Mouse MP 2200 Genes GS165465: MP:0003633 abnormal nervous system physiology
Expand Tier I Mouse 363 Genes GS136744: spermatogenesis defect 2 (Spmd2, Published QTL Chr 4)
Expand Tier I Human GO 205 Genes GS209987: GO:0050953 sensory perception of light stimulus
Expand Tier I Mouse MP 1724 Genes GS164220: MP:0002882 abnormal neuron morphology
Expand Tier I Mouse MP 1111 Genes GS166412: MP:0002118 abnormal lipid homeostasis
Expand Tier I Mouse MP 281 Genes GS163596: MP:0000026 abnormal inner ear morphology
Expand Tier I Mouse MP 610 Genes GS170086: MP:0000703 abnormal thymus morphology
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Mouse MP 369 Genes GS170089: MP:0000706 small thymus
Expand Tier II Mouse 74 Genes GS36513: Cerebellum Gene expression correlates of Dowel Test - Time 0 Sec in Females & Males BXD
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Mouse MP 396 Genes GS170108: MP:0003727 abnormal retinal layer morphology
Expand Tier I Mouse MP 466 Genes GS165253: MP:0001399 hyperactivity
Expand Tier I Mouse 356 Genes GS135525: body weight QTL 9 (Bwtq9, Published QTL Chr 4)
Expand Tier I Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Mouse MP 873 Genes GS165493: MP:0000653 abnormal sex gland morphology
Expand Tier I Mouse 3109 Genes GS127923: Cerebellum - Allen Mouse Brain Atlas
Expand Tier I Human GO 2661 Genes GS207797: GO:0030154 cell differentiation
Expand Tier I Human GO 4070 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Mouse MP 443 Genes GS163419: MP:0009209 abnormal internal female genitalia morphology
Expand Tier I Human GO 4024 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human GO 1287 Genes GS205610: GO:0044430 cytoskeletal part
Expand Tier I Mouse MP 282 Genes GS165049: MP:0004857 abnormal heart weight
Expand Tier I Mouse MP 230 Genes GS163320: MP:0000031 abnormal cochlea morphology
Expand Tier I Mouse GO 187 Genes GS187229: GO:0043583 ear development
Expand Tier I Mouse MP 3019 Genes GS165466: MP:0003632 abnormal nervous system morphology
Expand Tier I Mouse MP 1941 Genes GS165528: MP:0005379 endocrine/exocrine gland phenotype
Expand Tier I Mouse MP 1756 Genes GS163956: MP:0011180 abnormal hematopoietic cell number
Expand Tier I Mouse MP 2057 Genes GS169835: MP:0005389 reproductive system phenotype
Expand Tier I Mouse MP 471 Genes GS169228: MP:0001406 abnormal gait
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 3493 Genes GS177570: GO:0016043 cellular component organization
Expand Tier I Human GO 1789 Genes GS208893: GO:0005856 cytoskeleton
Expand Tier I Human 592 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Mouse MP 189 Genes GS168193: MP:0000966 decreased sensory neuron number
Expand Tier I Human GO 23 Genes GS204718: GO:0032391 photoreceptor connecting cilium
Expand Tier I Mouse MP 46 Genes GS165617: MP:0004398 cochlear inner hair cell degeneration
Expand Tier I Mouse MP 985 Genes GS167025: MP:0003953 abnormal hormone level
Expand Tier I Mouse MP 814 Genes GS163226: MP:0003312 abnormal locomotor coordination
Expand Tier I Human 344 Genes GS174378: HP:0000518 Cataract
Expand Tier I Mouse MP 94 Genes GS164629: MP:0005289 increased oxygen consumption
Expand Tier II Mouse 306 Genes GS84159: alcohol withdrawal (Published QTL, Chr 4)
Expand Tier I Human GO 495 Genes GS209225: GO:0007600 sensory perception
Expand Tier I Human 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human GO 435 Genes GS197802: GO:0007423 sensory organ development
Expand Tier I Human 416 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier I Human GO 20 Genes GS195928: GO:0060119 inner ear receptor cell development
Expand Tier I Mouse MP 6 Genes GS167405: MP:0004531 short outer hair cell stereocilia
Expand Tier I Mouse MP 165 Genes GS164953: MP:0002707 abnormal kidney weight
Expand Tier I Human 398 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Mouse MP 180 Genes GS163068: MP:0000045 abnormal hair cell morphology
Expand Tier I Mouse MP 262 Genes GS164126: MP:0001388 abnormal stationary movement
Expand Tier I Mouse GO 591 Genes GS182595: GO:0019904 protein domain specific binding
Expand Tier I Mouse MP 184 Genes GS164059: MP:0006325 impaired hearing
Expand Tier I Mouse MP 29 Genes GS168879: MP:0004737 absent distortion product otoacoustic emissions
Expand Tier I Human GO 3125 Genes GS197892: GO:0043228 non-membrane-bounded organelle
Expand Tier I Mouse 328 Genes GS129092: bone mechanical trait 2 (Bmch2 Published QTL Chr 4)
Expand Tier I Human GO 111 Genes GS201148: GO:0001894 tissue homeostasis
Expand Tier I Mouse 459 Genes GS129186: silicosis susceptibility 1 (Slcs1 Published QTL Chr 4)
Expand Tier I Mouse MP 3543 Genes GS169828: MP:0005386 behavior/neurological phenotype
Expand Tier I Mouse 359 Genes GS135467: blood pressure QTL 3 (Bpq3, Published QTL Chr 4)
Expand Tier I Mouse 3289 Genes GS127932: Pallidum - Allen Mouse Brain Atlas
Expand Tier I Mouse MP 983 Genes GS166244: MP:0002752 abnormal somatic nervous system morphology
Expand Tier I Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Mouse 370 Genes GS136965: weight loss response 3 (Wtlr3, Published QTL Chr 4)
Expand Tier I Mouse MP 365 Genes GS168326: MP:0002706 abnormal kidney size
Expand Tier I Mouse 378 Genes GS135376: body length 6 (Bdln6, Published QTL Chr 4)
Expand Tier I Human 202 Genes GS174764: HP:0007367 Atrophy/Degeneration affecting the central nervous system
Expand Tier I Mouse MP 3716 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier I Human 472 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Mouse 280 Genes GS136776: synechia 2 (Synch2, Published QTL Chr 4)
Expand Tier I Mouse MP 1856 Genes GS165386: MP:0001262 decreased body weight
Expand Tier I Mouse MP 1222 Genes GS165535: MP:0005370 liver/biliary system phenotype
Expand Tier I Mouse 357 Genes GS136231: mandible length 5 (Manln5, Published QTL Chr 4)
Expand Tier I Human 364 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Mouse MP 2406 Genes GS169391: MP:0002066 abnormal motor capabilities/coordination/movement
Expand Tier I Mouse MP 898 Genes GS169390: MP:0002067 abnormal sensory capabilities/reflexes/nociception
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 Mouse GO 781 Genes GS184010: GO:0030030 cell projection organization
Expand Tier I Human 512 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Mouse MP 57 Genes GS164481: MP:0001745 increased circulating corticosterone level
Expand Tier I Human GO 68 Genes GS204815: GO:0005902 microvillus
Expand Tier I Mouse 378 Genes GS136620: sucrose consumption 1 (Scon1, Published QTL Chr 4)
Expand Tier I Human 79 Genes GS173104: HP:0000670 Carious teeth
Expand Tier I Mouse MP 1086 Genes GS165869: MP:0002138 abnormal hepatobiliary system morphology
Expand Tier I Mouse GO 609 Genes GS185024: GO:0044463 cell projection part
Expand Tier I Human GO 3513 Genes GS193991: GO:0048731 system development
Expand Tier I Mouse 3395 Genes GS127929: Medulla - Allen Mouse Brain Atlas
Expand Tier I Mouse MP 22 Genes GS168524: MP:0004905 decreased uterus weight
Expand Tier I Mouse MP 495 Genes GS166123: MP:0002102 abnormal ear morphology
Expand Tier I Mouse MP 779 Genes GS163916: MP:0009198 abnormal male genitalia morphology
Expand Tier I Human GO 238 Genes GS196129: GO:0005929 cilium
Expand Tier I Mouse GO 2138 Genes GS186067: GO:0050877 neurological system process
Expand Tier I Human GO 312 Genes GS206305: GO:0044297 cell body
Expand Tier I Mouse MP 14 Genes GS165668: MP:0004524 short cochlear hair cell stereocilia
Expand Tier II Mouse 249 Genes GS35944: Striatum Gene expression correlates of Handling induced convulsion baseline in Females & Males BXD
Expand Tier I Mouse GO 2498 Genes GS193018: GO:0003008 system process
Expand Tier I Human GO 637 Genes GS201839: GO:0044463 cell projection part
Expand Tier I Mouse MP 2754 Genes GS169767: MP:0002396 abnormal hematopoietic system morphology/development
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Mouse MP 43 Genes GS169994: MP:0004956 decreased thymus weight
Expand Tier I Mouse MP 89 Genes GS168522: MP:0004907 abnormal seminal vesicle size
Expand Tier I Mouse GO 2872 Genes GS178360: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Mouse 378 Genes GS136016: heart failure modifier 3 (Hrtfm3, Published QTL Chr 4)
Expand Tier II Mouse 21 Genes GS35024: Striatum Gene expression correlates of Percentage of time into open arms of plus maze in Females & Males BXD
Expand Tier I Mouse 307 Genes GS136845: thymic lymphoma suppressor region 4 (Tlsr4, Published QTL Chr 4)
Expand Tier I Human GO 2545 Genes GS203335: GO:0048513 organ development
Expand Tier I Mouse 362 Genes GS135329: autoimmune renal vasculitis 1 (Arvm1, Published QTL Chr 4)
Expand Tier I Human 607 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Mouse MP 445 Genes GS163240: MP:0002364 abnormal thymus size
Expand Tier I Human GO 291 Genes GS199165: GO:0043025 neuronal cell body
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier III Rat 904 Genes GS137847: Genes linked to age-related cognitive impairment in the hippocampi of young vs. aged cognitively impaired (AI) vs. aged cognitively unimpaired (AU) rats
Expand Tier I Human 388 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Mouse 361 Genes GS136182: lymphoproliferation modifier 1 (Lprm1, Published QTL Chr 4)
Expand Tier I Mouse MP 1419 Genes GS163818: MP:0002722 abnormal immune system organ morphology
Expand Tier I Human GO 1191 Genes GS207015: GO:0042592 homeostatic process
Expand Tier I Mouse GO 792 Genes GS190899: GO:0043005 neuron projection
Expand Tier I Human 42 Genes GS174449: HP:0001123 Visual field defect
Expand Tier I Human 414 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Mouse MP 2099 Genes GS165616: MP:0002127 abnormal cardiovascular system morphology
Expand Tier I Mouse 362 Genes GS136759: soft tissue heal 3 (Stheal3, Published QTL Chr 4)
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Mouse GO 28 Genes GS181643: GO:0032421 stereocilium bundle
Expand Tier I Human 90 Genes GS170889: HP:0006482 Abnormality of dental morphology
Expand Tier I Mouse GO 2876 Genes GS182474: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier I Mouse MP 50 Genes GS167465: MP:0004910 decreased seminal vesicle weight
Expand Tier I Mouse MP 143 Genes GS169847: MP:0004399 abnormal cochlear outer hair cell morphology
Expand Tier I Mouse MP 710 Genes GS167922: MP:0000959 abnormal somatic sensory system morphology
Expand Tier I Mouse MP 1740 Genes GS166710: MP:0002163 abnormal gland morphology
Expand Tier I Mouse GO 326 Genes GS185304: GO:0030424 axon
Expand Tier I Mouse GO 23 Genes GS187859: GO:0032391 photoreceptor connecting cilium
Expand Tier I Human GO 132 Genes GS209984: GO:0050954 sensory perception of mechanical stimulus
Expand Tier I Mouse GO 27 Genes GS179162: GO:0060119 inner ear receptor cell development
Expand Tier I Mouse MP 290 Genes GS168682: MP:0000599 enlarged liver
Expand Tier I Human GO 23 Genes GS198432: GO:0032420 stereocilium
Expand Tier I Mouse 883 Genes GS129123: cataract severity (Ctrcts Published QTL Chr 4)
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Mouse MP 14488 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Human GO 541 Genes GS199393: GO:0019904 protein domain specific binding
Expand Tier I Mouse MP 1098 Genes GS163026: MP:0000221 decreased leukocyte cell number
Expand Tier I Mouse GO 403 Genes GS185303: GO:0030425 dendrite
Expand Tier II Mouse 369 Genes GS84157: METH responses for chewing (Published QTL, Chr 4)
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier II Mouse 335 Genes GS84158: cocaine related behavior (Published QTL, Cocrb5, Chr 4)
Expand Tier I Mouse MP 56 Genes GS169992: MP:0004954 abnormal thymus weight
Expand Tier I Mouse MP 652 Genes GS170577: MP:0005406 abnormal heart size
Expand Tier I Mouse 364 Genes GS135709: diabetes susceptibility QTL 6 (Dbsq6, Published QTL Chr 4)
Expand Tier I Mouse GO 4 Genes GS182628: GO:0002142 stereocilia ankle link complex
Expand Tier I Mouse GO 3605 Genes GS190682: GO:0007275 multicellular organismal development
Expand Tier I Mouse GO 1681 Genes GS191954: GO:0005856 cytoskeleton
Expand Tier I Mouse MP 2419 Genes GS168551: MP:0002429 abnormal blood cell morphology/development
Expand Tier I Mouse MP 98 Genes GS165787: MP:0001522 impaired swimming
Expand Tier I Human 96 Genes GS176616: HP:0000662 Night blindness
Expand Tier I Mouse GO 4 Genes GS182620: GO:0002141 stereocilia ankle link
Expand Tier I Mouse MP 314 Genes GS169915: MP:0005560 decreased circulating glucose level
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 I Mouse MP 34 Genes GS167452: MP:0004532 abnormal inner hair cell stereociliary bundle morphology
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Mouse MP 1521 Genes GS163297: MP:0000217 abnormal leukocyte cell number
Expand Tier I Mouse MP 37 Genes GS168518: MP:0004903 abnormal uterus weight
Expand Tier I Mouse 365 Genes GS136394: organ weight 3 (Org3, Published QTL Chr 4)
Expand Tier I Mouse GO 1550 Genes GS192290: GO:0007600 sensory perception
Expand Tier I Mouse MP 98 Genes GS166700: MP:0003963 abnormal corticosterone level
Expand Tier I Mouse MP 1672 Genes GS165260: MP:0001392 abnormal locomotor behavior
Expand Tier I Mouse 362 Genes GS135796: ethanol induced low dose activation 4 (Elda4, Published QTL Chr 4)
Expand Tier I Human GO 56 Genes GS197007: GO:0005884 actin filament
Expand Tier I Mouse MP 12 Genes GS165679: MP:0004529 decreased outer hair cell stereocilia number
Expand Tier I Mouse MP 1385 Genes GS163971: MP:0002092 abnormal eye morphology
Expand Tier I Mouse MP 115 Genes GS169841: MP:0004393 abnormal cochlear inner hair cell morphology
Expand Tier I Mouse MP 553 Genes GS165385: MP:0008946 abnormal neuron number
Expand Tier I Mouse MP 2606 Genes GS165397: MP:0001265 decreased body size
Expand Tier I Mouse MP 344 Genes GS168218: MP:0001963 abnormal hearing physiology
Expand Tier I Mouse MP 123 Genes GS167220: MP:0001326 retinal degeneration
Expand Tier I Human GO 1236 Genes GS202899: GO:0050877 neurological system process
Expand Tier I Human GO 794 Genes GS209568: GO:0048666 neuron development
Expand Tier I Mouse MP 183 Genes GS165255: MP:0001394 circling
Expand Tier I Human 578 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Mouse 378 Genes GS136715: susceptibility to lung cancer 18 (Sluc18, Published QTL Chr 4)
Expand Tier I Mouse MP 451 Genes GS163418: MP:0009208 abnormal female genitalia morphology
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Mouse GO 4 Genes GS181740: GO:0002139 stereocilia coupling link
Expand Tier I Mouse MP 96 Genes GS168183: MP:0003917 increased kidney weight
Expand Tier I Mouse MP 157 Genes GS167787: MP:0008779 abnormal maternal behavior
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Mouse MP 4592 Genes GS165537: MP:0005376 homeostasis/metabolism phenotype
Expand Tier I Mouse GO 87 Genes GS190034: GO:0031513 nonmotile primary cilium
Expand Tier I Mouse MP 167 Genes GS169397: MP:0002068 abnormal parental behavior
Expand Tier I Human GO 1693 Genes GS209960: GO:0003008 system process
Expand Tier I Mouse MP 182 Genes GS163063: MP:0000042 abnormal organ of Corti morphology
Expand Tier I Human 168 Genes GS175668: HP:0007369 Atrophy/Degeneration affecting the cerebrum
Expand Tier I Mouse MP 875 Genes GS168958: MP:0003492 abnormal involuntary movement
Expand Tier I Mouse 357 Genes GS136879: tooth shape 5 (Tshp5, Published QTL Chr 4)
Expand Tier I Mouse MP 152 Genes GS165463: MP:0001523 impaired righting response
Expand Tier I Mouse 459 Genes GS129188: spermatogenesis defect 1 (Spmd1 Published QTL Chr 4)
Expand Tier I Mouse GO 159 Genes GS179560: GO:0048839 inner ear development
Expand Tier I Human GO 6278 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function