Gene Details



Pcdh15 and homologs in 5 species are found in 457 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 182 Genes GS168433: MP:0002980 abnormal postural reflex
Expand Tier I Mouse MP 50 Genes GS167803: MP:0005307 head tossing
Expand Tier I Mouse 558 Genes GS135258: anti-erythrocyte autoantibody modifier 3 (Aem3, Published QTL Chr 10)
Expand Tier I Mouse 515 Genes GS135860: femur breaking strength 3 (Fembrs3, Published QTL Chr 10)
Expand Tier I Mouse GO 152 Genes GS193051: GO:0051606 detection of stimulus
Expand Tier I Mouse GO 763 Genes GS191625: GO:0040007 growth
Expand Human 18 Genes GS219748: http://www.broadinstitute.org/gsea/msigdb/cards/SYNAPSE
Expand Tier I Mouse GO 6 Genes GS188267: GO:0035058 nonmotile primary cilium assembly
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 58 Genes GS165022: MP:0002857 cochlear ganglion degeneration
Expand Tier I Human CTD 200 Genes GS125369: Lamivudine interacting genes (MeSH:D019259) in CTD
Expand Tier II Mouse 358 Genes GS35852: Striatum Gene expression correlates of Cocaine CPP - difference in time spent relative to baseline drug exposure in Males BXD
Expand Tier I Mouse MP 25 Genes GS167764: MP:0004491 abnormal orientation of outer hair cell stereociliary bundles
Expand Tier I Mouse 515 Genes GS136052: IGF-1 serum levels 2 (Igf1sl2, Published QTL Chr 10)
Expand Tier I Human CTD 62 Genes GS125368: Saquinavir interacting genes (MeSH:D019258) in CTD
Expand Tier I Human 379 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Human GO 124 Genes GS210482: GO:0007605 sensory perception of sound
Expand Tier I Mouse MP 10 Genes GS166797: MP:0003143 enlarged otoliths
Expand Tier I Human GO 954 Genes GS195976: GO:0007155 cell adhesion
Expand Tier I Human GO 854 Genes GS203972: GO:0005615 extracellular space
Expand Tier I Mouse 500 Genes GS136165: leishmaniasis resistance 19 (Lmr19, Published QTL Chr 10)
Expand Tier I Mouse 558 Genes GS135790: epilepsy 3 (El3, Published QTL Chr 10)
Expand Tier I Human 12 Genes GS171801: HP:0008527 Congenital sensorineural hearing impairment
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 536 Genes GS135751: experimental allergic encephalomyelitis susceptibility 17 (Eae17, Published QTL Chr 10)
Expand Tier I Mouse MP 51 Genes GS164837: MP:0006359 absent startle reflex
Expand Tier I Mouse GO 3615 Genes GS178359: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human GO 204 Genes GS210485: GO:0007601 visual perception
Expand Tier I Mouse GO 3597 Genes GS188142: GO:0048856 anatomical structure development
Expand Tier III Mouse 69 Genes GS34463: Whole Brain Gene expression correlates of Novel environment locomotion (activity beam breaks) 15-30 min in the periphery in BXD Males
Expand Tier I Mouse MP 173 Genes GS168066: MP:0002622 abnormal cochlear hair cell morphology
Expand Tier I Mouse 493 Genes GS136910: vertebral morphology and mechanical traits 15 (Vmmt15, Published QTL Chr 10)
Expand Tier I Mouse MP 169 Genes GS165461: MP:0001525 impaired balance
Expand Tier I Mouse MP 58 Genes GS168293: MP:0004742 abnormal vestibular system physiology
Expand Tier I Mouse GO 2762 Genes GS178357: GO:0071842 cellular component organization at cellular level
Expand Tier I Mouse MP 1082 Genes GS166660: MP:0001731 abnormal postnatal growth
Expand Tier I Mouse MP 202 Genes GS166905: MP:0001486 abnormal startle reflex
Expand Tier I Human GO 4371 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Human GO 38 Genes GS198664: GO:0043954 cellular component maintenance
Expand Tier I Human 50 Genes GS173812: HP:0000738 Hallucinations
Expand Tier I Mouse GO 912 Genes GS179236: GO:0048699 generation of neurons
Expand Human 622 Genes GS219996: http://www.broadinstitute.org/gsea/msigdb/cards/NON_MEMBRANE_BOUND_ORGANELLE
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Mouse 3319 Genes GS127931: Olfactory bulb - Allen Mouse Brain Atlas
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Mouse GO 126 Genes GS178730: GO:0030534 adult behavior
Expand Tier I Mouse GO 758 Genes GS188757: GO:0009887 organ morphogenesis
Expand Tier I Mouse MP 33 Genes GS168674: MP:0002895 abnormal otolithic membrane morphology
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 MP 30 Genes GS165256: MP:0001395 bidirectional circling
Expand Tier I Mouse MP 380 Genes GS165261: MP:0001393 ataxia
Expand Tier I Mouse 515 Genes GS135323: apomorphine stress induced climbing 3 (Apsic3, Published QTL Chr 10)
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
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 530 Genes GS136631: small effect CIA locus 5 (Secia5, Published QTL Chr 10)
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier I Mouse GO 560 Genes GS189224: GO:0007610 behavior
Expand Tier I Mouse 2963 Genes GS127934: Retrohippocampal region - Allen Mouse Brain Atlas
Expand Tier I Mouse MP 42 Genes GS164347: MP:0006334 abnormal susceptibility to hearing loss
Expand Tier I Mouse GO 6473 Genes GS184448: GO:0044425 membrane part
Expand Tier I Mouse GO 639 Genes GS192628: GO:0048666 neuron development
Expand Tier I Human GO 4097 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human GO 5810 Genes GS206742: GO:0043167 ion binding
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 Mouse MP 268 Genes GS164346: MP:0006335 abnormal hearing electrophysiology
Expand Tier I Human 32 Genes GS175414: HP:0008619 Bilateral sensorineural hearing impairment
Expand Tier I Mouse GO 24 Genes GS186963: GO:0045494 photoreceptor cell maintenance
Expand Tier I Human GO 45 Genes GS197327: GO:0050885 neuromuscular process controlling balance
Expand Tier I Mouse GO 903 Genes GS191212: GO:0009605 response to external stimulus
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Mouse GO 10879 Genes GS181473: GO:0005488 binding
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
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 7808 Genes GS207616: GO:0016020 membrane
Expand Tier I Mouse MP 3437 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Mouse GO 77 Genes GS183900: GO:0009582 detection of abiotic stimulus
Expand Tier I Mouse MP 648 Genes GS164023: MP:0001961 abnormal reflex
Expand Tier I Mouse GO 88 Genes GS188110: GO:0050905 neuromuscular process
Expand Tier I Mouse MP 8 Genes GS167119: MP:0004577 abnormal cochlear hair cell inter-stereocilial links morphology
Expand Tier I Mouse MP 4173 Genes GS165527: MP:0005378 growth/size phenotype
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Mouse GO 138 Genes GS177976: GO:0035264 multicellular organism growth
Expand Tier I Mouse GO 554 Genes GS188813: GO:0045202 synapse
Expand Tier I Mouse 3267 Genes GS127938: Striatum - Allen Mouse Brain Atlas
Expand Tier I Mouse MP 13 Genes GS163801: MP:0003637 cochlear ganglion hypoplasia
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 Human 89 Genes GS173329: HP:0000682 Abnormality of dental enamel
Expand Human 622 Genes GS219919: http://www.broadinstitute.org/gsea/msigdb/cards/INTRACELLULAR_NON_MEMBRANE_BOUND_ORGANELLE
Expand Tier I Mouse GO 68 Genes GS188314: GO:0007156 homophilic cell adhesion
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 37 Genes GS165664: MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles
Expand Tier I Mouse GO 785 Genes GS187113: GO:0005615 extracellular space
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 Mouse 537 Genes GS136778: systolic blood pressure 1 (Sysbp1, Published QTL Chr 10)
Expand Tier I Mouse GO 1204 Genes GS188763: GO:0009888 tissue development
Expand Tier I Mouse GO 815 Genes GS179210: GO:0007155 cell adhesion
Expand Tier I Mouse GO 133 Genes GS193043: GO:0050954 sensory perception of mechanical stimulus
Expand Tier I Mouse GO 26 Genes GS185005: GO:0050974 detection of mechanical stimulus involved in sensory perception
Expand Tier I Human 34 Genes GS172732: HP:0001751 Vestibular dysfunction
Expand Tier I Human 220 Genes GS171791: HP:0000370 Abnormality of the middle ear
Expand Tier I Mouse MP 3110 Genes GS167020: MP:0003956 abnormal body size
Expand Human 622 Genes GS219918: http://www.broadinstitute.org/gsea/msigdb/cards/NON_MEMBRANE_BOUND_ORGANELLE
Expand Tier I Mouse 3096 Genes GS127928: Lateral septal complex - Allen Mouse Brain Atlas
Expand Tier II Mouse 69 Genes GS34462: Whole Brain Gene expression correlates of Novel environment locomotion (activity beam breaks) 15-30 min in the periphery in Males BXD
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human GO 78 Genes GS206917: GO:0031513 nonmotile primary cilium
Expand Tier I Human CTD 377 Genes GS121976: Zidovudine interacting genes (MeSH:D015215) in CTD
Expand Tier I Mouse GO 37 Genes GS181873: GO:0043954 cellular component maintenance
Expand Tier I Mouse GO 7 Genes GS192719: GO:0060013 righting reflex
Expand Tier I Mouse GO 621 Genes GS180679: GO:0009628 response to abiotic stimulus
Expand Tier I Mouse 2918 Genes GS127935: Striatum dorsal region - Allen Mouse Brain Atlas
Expand Tier I Mouse MP 438 Genes GS165390: MP:0003224 neuron degeneration
Expand Tier II Mouse 479 Genes GS36760: Hippocampus Gene expression correlates of Vocalization Threshold - shock intensity (mA) in Males BXD
Expand Tier I Mouse MP 44 Genes GS167233: MP:0004300 abnormal organ of Corti supporting cell morphology
Expand Tier I Mouse 558 Genes GS135635: collagen induced arthritis QTL 8 (Cia8, Published QTL Chr 10)
Expand Tier I Human 157 Genes GS171968: HP:0000405 Conductive hearing impairment
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier III Human 69 Genes GS14908: Nicotine Abstinence Genes found in Genome-wide Association Studies (GWAS)
Expand Tier I Mouse MP 26 Genes GS170347: MP:0004748 increased susceptibility to age-related hearing loss
Expand Tier I Human 93 Genes GS176289: HP:0002120 Cerebral cortical atrophy
Expand Tier I Mouse 545 Genes GS135699: directional asymmetry QTL 6 (Daq6, Published QTL Chr 10)
Expand Tier I Mouse GO 2538 Genes GS190893: GO:0030154 cell differentiation
Expand Tier I Mouse GO 478 Genes GS187648: GO:0048729 tissue morphogenesis
Expand Tier I Human GO 4283 Genes GS197009: GO:0005886 plasma membrane
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
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 Mouse GO 96 Genes GS183899: GO:0009581 detection of external stimulus
Expand Tier I Mouse 536 Genes GS135438: bone mineral density 38 (Bmd38, Published QTL Chr 10)
Expand Tier I Mouse MP 5 Genes GS163827: MP:0011062 abnormal outer hair cell kinocilium morphology
Expand Tier I Human 416 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier I Mouse 515 Genes GS136941: vertebral trabecular bone trait 9 (Vtbt9, Published QTL Chr 10)
Expand Tier I Mouse GO 5879 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Mouse MP 11 Genes GS163829: MP:0011060 abnormal kinocilium morphology
Expand Tier I Mouse MP 17 Genes GS165666: MP:0004523 decreased cochlear hair cell stereocilia number
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 Human GO 956 Genes GS200151: GO:0022610 biological adhesion
Expand Tier I Mouse MP 86 Genes GS167643: MP:0000034 abnormal vestibule morphology
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Mouse MP 113 Genes GS168215: MP:0001967 deafness
Expand Tier I Human GO 3125 Genes GS199272: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier II Mouse 40 Genes GS26241: Hippocampus Gene expression correlates of Mechanical Nociception - Tail Clip Test in Females BXD
Expand Tier I Mouse GO 6204 Genes GS184629: GO:0005515 protein binding
Expand Tier I Mouse MP 181 Genes GS163498: MP:0003308 abnormal cochlear sensory epithelium morphology
Expand Tier I Mouse 493 Genes GS135614: circulating hormone level QTL 6 (Chlq6, Published QTL Chr 10)
Expand Tier I Mouse MP 295 Genes GS169967: MP:0001408 stereotypic behavior
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 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 II Mouse 521 Genes GS84241: alcohol preference (Published QTL, Chr 10)
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 GO 359 Genes GS192629: GO:0048667 cell morphogenesis involved in neuron differentiation
Expand Tier I Mouse 514 Genes GS136397: organ weight 6 (Org6, Published QTL Chr 10)
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Mouse 558 Genes GS136076: insulin QTL 9 (Insq9, Published QTL Chr 10)
Expand Tier I Mouse MP 63 Genes GS169793: MP:0004425 abnormal otolith organ morphology
Expand Human 622 Genes GS219701: http://www.broadinstitute.org/gsea/msigdb/cards/NON_MEMBRANE_BOUND_ORGANELLE
Expand Tier I Human GO 25 Genes GS203824: GO:0045494 photoreceptor cell maintenance
Expand Tier I Mouse GO 15 Genes GS180171: GO:0060122 inner ear receptor stereocilium organization
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 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 GO 92 Genes GS180716: GO:0042472 inner ear morphogenesis
Expand Tier I Mouse GO 2876 Genes GS181102: GO:0043228 non-membrane-bounded organelle
Expand Tier I Mouse GO 123 Genes GS193540: GO:0007601 visual perception
Expand Tier I Mouse MP 152 Genes GS165463: MP:0001523 impaired righting response
Expand Tier I Mouse GO 159 Genes GS179560: GO:0048839 inner ear development
Expand Tier I Mouse MP 1007 Genes GS164742: MP:0001732 postnatal growth retardation
Expand Tier I Mouse MP 14 Genes GS167765: MP:0004492 abnormal orientation of inner hair cell stereociliary bundles
Expand Tier I Mouse GO 5859 Genes GS182404: GO:0031224 intrinsic to membrane
Expand Tier I Mouse 3289 Genes GS127924: Cerebral cortex - Allen Mouse Brain Atlas
Expand Tier I Mouse 3384 Genes GS127925: Hippocampal formation - Allen Mouse Brain Atlas
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
Expand Tier I Human GO 404 Genes GS204214: GO:0016337 cell-cell adhesion
Expand Tier I Mouse 539 Genes GS135326: age related thymic involution 2 (Arti2, Published QTL Chr 10)
Expand Tier I Mouse MP 19 Genes GS170320: MP:0004813 absent linear vestibular evoked potential
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 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 Mouse GO 1466 Genes GS180001: GO:0048646 anatomical structure formation involved in morphogenesis
Expand Tier I Mouse 539 Genes GS135585: cholesterol absorption 2 (Chab2, Published QTL Chr 10)
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 Human 255 Genes GS176610: HP:0003593 Infantile onset
Expand Tier I Mouse MP 28 Genes GS164033: MP:0004812 abnormal linear vestibular evoked potential
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 585 Genes GS165985: MP:0000965 abnormal sensory neuron morphology
Expand Tier I Mouse GO 9 Genes GS187246: GO:0060088 auditory receptor cell stereocilium organization
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 GO 2 Genes GS191056: GO:0050973 detection of mechanical stimulus involved in equilibrioception
Expand Tier I Mouse GO 11 Genes GS189304: GO:0002093 auditory receptor cell morphogenesis
Expand Tier I Mouse GO 15 Genes GS189630: GO:0060117 auditory receptor cell development
Expand Tier I Mouse GO 49 Genes GS185850: GO:0060113 inner ear receptor cell differentiation
Expand Tier I Mouse 2944 Genes GS127937: Striatum-like amygdalar nuclei - Allen Mouse Brain Atlas
Expand Tier I Mouse MP 87 Genes GS165544: MP:0004362 cochlear hair cell degeneration
Expand Tier I Mouse MP 1013 Genes GS164724: MP:0001516 abnormal motor coordination/ balance
Expand Tier I Mouse 551 Genes GS136151: "lupus in MRL and B6 F2 cross, QTL 4" (Lmb4, Published QTL Chr 10)
Expand Tier I Mouse GO 36 Genes GS185506: GO:0007628 adult walking behavior
Expand Tier II Mouse 416 Genes GS36158: Neocortex Gene expression correlates of Locomotor response of 10 mg/kg MDMA injected on Day 2 in Females BXD
Expand Tier I Mouse 2962 Genes GS127936: Striatum ventral region - Allen Mouse Brain Atlas
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 MP 1825 Genes GS168956: MP:0003491 abnormal voluntary movement
Expand Tier I Mouse GO 8145 Genes GS190714: GO:0016020 membrane
Expand Tier I Mouse 537 Genes GS136675: skull morphology 14 (Skull14, Published QTL Chr 10)
Expand Tier I Mouse GO 1394 Genes GS191552: GO:0042995 cell projection
Expand Tier I Mouse 493 Genes GS135606: circulating hormone level QTL 15 (Chlq15, Published QTL Chr 10)
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
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 Human 143 Genes GS176586: HP:0001270 Motor delay
Expand Tier I Mouse MP 18 Genes GS162895: MP:0003986 small cochlear ganglion
Expand Tier I Mouse MP 18 Genes GS170740: MP:0003825 abnormal pillar cell morphology
Expand Tier II Mouse 18 Genes GS35418: Neocortex Gene expression correlates of Zero Maze - Latency to enter an open quadrant in Females & Males BXD
Expand Tier I Mouse GO 379 Genes GS187166: GO:0044708 single-organism behavior
Expand Tier I Human 381 Genes GS175714: HP:0011389 Functional abnormality of the inner ear
Expand Tier I Mouse MP 249 Genes GS163316: MP:0000035 abnormal membranous labyrinth morphology
Expand Tier I Mouse GO 395 Genes GS188268: GO:0030029 actin filament-based process
Expand Tier I Human 41 Genes GS176115: HP:0000540 Hypermetropia
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
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 GO 6947 Genes GS192918: GO:0050896 response to stimulus
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 GO 112 Genes GS180713: GO:0042471 ear morphogenesis
Expand Tier I Mouse MP 174 Genes GS165804: MP:0002862 altered righting response
Expand Tier I Mouse GO 63 Genes GS184782: GO:0009612 response to mechanical stimulus
Expand Tier I Mouse 3315 Genes GS127939: Thalamus - Allen Mouse Brain Atlas
Expand Tier I Mouse GO 8 Genes GS193044: GO:0050957 equilibrioception
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 164 Genes GS163724: MP:0000436 abnormal head movements
Expand Tier III Human 107 Genes GS14904: Genes Harboring Allelic Variants That Distinguish Successful vs Unsuccessful Nicotine Abstainers in at Least 2 Samples
Expand Tier I Mouse GO 55 Genes GS188801: GO:0042490 mechanoreceptor differentiation
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 Mouse GO 192 Genes GS179167: GO:0007015 actin filament organization
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 I Mouse GO 926 Genes GS178355: GO:0071844 cellular component assembly at cellular level
Expand Tier III Mouse 69 Genes GS34483: Whole Brain Gene expression correlates of Novel environment locomotion (activity beam breaks) 15-30 min in the periphery [Cocaine] in Males BXD
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 GO 70 Genes GS188107: GO:0050906 detection of stimulus involved in sensory perception
Expand Tier I Mouse GO 18 Genes GS188400: GO:0060004 reflex
Expand Tier I Human GO 140 Genes GS205171: GO:0007156 homophilic cell adhesion
Expand Tier I Mouse MP 61 Genes GS167666: MP:0000032 cochlear degeneration
Expand Tier I Mouse 3343 Genes GS127930: Midbrain - Allen Mouse Brain Atlas
Expand Tier I Mouse 3329 Genes GS127933: Pons - Allen Mouse Brain Atlas
Expand Tier I Human 172 Genes GS173476: HP:0002311 Incoordination
Expand Tier I Human GO 8 Genes GS209985: GO:0050957 equilibrioception
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 GO 747 Genes GS193294: GO:0000902 cell morphogenesis
Expand Tier I Human CTD 1551 Genes GS125506: Valproic Acid interacting genes (MeSH:D014635) in CTD
Expand Tier I Human GO 205 Genes GS209987: GO:0050953 sensory perception of light stimulus
Expand Tier I Mouse GO 72 Genes GS181684: GO:0042384 cilium assembly
Expand Tier I Mouse 537 Genes GS136454: postnatal body weight growth 16 (Pbwg16, Published QTL Chr 10)
Expand Tier I Mouse MP 1724 Genes GS164220: MP:0002882 abnormal neuron morphology
Expand Tier I Mouse MP 281 Genes GS163596: MP:0000026 abnormal inner ear morphology
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Mouse GO 711 Genes GS179173: GO:0007010 cytoskeleton organization
Expand Tier I Mouse GO 3706 Genes GS188641: GO:0071944 cell periphery
Expand Tier I Mouse MP 1 Genes GS165766: MP:0004303 abnormal Hensen cell morphology
Expand Tier I Mouse 558 Genes GS135645: cardiac modifier of nmd 2 (Cmn2, Published QTL Chr 10)
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Mouse GO 3537 Genes GS192041: GO:0043169 cation binding
Expand Tier I Mouse MP 466 Genes GS165253: MP:0001399 hyperactivity
Expand Tier I Mouse 537 Genes GS136079: juvenile cystic kidney modifier 1 (Jckm1, Published QTL Chr 10)
Expand Tier I Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Mouse MP 5 Genes GS163828: MP:0011061 abnormal inner hair cell kinocilium morphology
Expand Tier I Mouse GO 123 Genes GS193046: GO:0050953 sensory perception of light stimulus
Expand Tier I Mouse 3109 Genes GS127923: Cerebellum - Allen Mouse Brain Atlas
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Mouse GO 5734 Genes GS190713: GO:0016021 integral to membrane
Expand Tier I Mouse GO 528 Genes GS180296: GO:0005509 calcium ion binding
Expand Tier I Mouse GO 1464 Genes GS182313: GO:0044085 cellular component biogenesis
Expand Tier I Mouse GO 1870 Genes GS192986: GO:0006996 organelle organization
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 30 Genes GS163925: MP:0002894 abnormal otolith morphology
Expand Tier I Mouse MP 3019 Genes GS165466: MP:0003632 abnormal nervous system morphology
Expand Tier I Human CTD 738 Genes GS126989: Hydralazine interacting genes (MeSH:D006830) in CTD
Expand Tier I Mouse MP 471 Genes GS169228: MP:0001406 abnormal gait
Expand Tier I Mouse MP 190 Genes GS169758: MP:0004765 decreased brainstem auditory evoked potential
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 Mouse GO 808 Genes GS192584: GO:0032989 cellular component morphogenesis
Expand Tier I Human 592 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Mouse GO 3442 Genes GS181533: GO:0046872 metal ion binding
Expand Tier I Mouse MP 90 Genes GS169795: MP:0004427 abnormal vestibular labyrinth morphology
Expand Tier I Mouse GO 366 Genes GS184013: GO:0030036 actin cytoskeleton organization
Expand Tier I Mouse MP 46 Genes GS165617: MP:0004398 cochlear inner hair cell degeneration
Expand Tier I Mouse GO 348 Genes GS181267: GO:0048568 embryonic organ development
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
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 Human GO 495 Genes GS209225: GO:0007600 sensory perception
Expand Tier I Human GO 37 Genes GS202821: GO:0001750 photoreceptor outer segment
Expand Tier I Human 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Mouse 546 Genes GS135360: B.burgdorferi-associated arthritis 18 (Bbaa18, Published QTL Chr 10)
Expand Tier I Mouse GO 500 Genes GS185033: GO:0048598 embryonic morphogenesis
Expand Tier I Human 416 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier I Mouse GO 822 Genes GS183355: GO:0022610 biological adhesion
Expand Tier I Mouse GO 469 Genes GS188136: GO:0048858 cell projection morphogenesis
Expand Tier I Mouse 317 Genes GS135697: directional asymmetry QTL 4 (Daq4, Published QTL Chr 10)
Expand Tier II Mouse 45 Genes GS35954: Hippocampus Gene expression correlates of Handling induced convulsion baseline in Males BXD
Expand Tier I Human 28 Genes GS173589: HP:0008513 Bilateral conductive hearing impairment
Expand Tier I Human GO 4034 Genes GS208978: GO:0043169 cation binding
Expand Tier I Mouse MP 180 Genes GS163068: MP:0000045 abnormal hair cell morphology
Expand Tier I Mouse 537 Genes GS136122: life span 2 (Lifespan2, Published QTL Chr 10)
Expand Human 18 Genes GS219965: http://www.broadinstitute.org/gsea/msigdb/cards/SYNAPSE
Expand Tier I Mouse MP 262 Genes GS164126: MP:0001388 abnormal stationary movement
Expand Tier I Mouse 536 Genes GS136154: limb length QTL 4 (Lmblgq4, Published QTL Chr 10)
Expand Tier I Mouse MP 184 Genes GS164059: MP:0006325 impaired hearing
Expand Tier I Human GO 3125 Genes GS197892: GO:0043228 non-membrane-bounded organelle
Expand Tier I Mouse GO 903 Genes GS184317: GO:0009790 embryo development
Expand Tier I Mouse 3136 Genes GS127926: Hippocampal region - Allen Mouse Brain Atlas
Expand Tier I Mouse MP 3543 Genes GS169828: MP:0005386 behavior/neurological phenotype
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 Mouse 317 Genes GS135698: directional asymmetry QTL 5 (Daq5, Published QTL Chr 10)
Expand Tier I Mouse GO 5225 Genes GS189860: GO:0043167 ion binding
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
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 Mouse 537 Genes GS136004: hepatocarcinogen resistance 2 (Hpcr2, Published QTL Chr 10)
Expand Tier I Mouse GO 15 Genes GS192427: GO:0050910 detection of mechanical stimulus involved in sensory perception of sound
Expand Tier I Mouse 558 Genes GS135312: aortic lesion size 1 (Aorls1, Published QTL Chr 10)
Expand Tier I Mouse GO 561 Genes GS182820: GO:0060429 epithelium development
Expand Tier I Mouse MP 88 Genes GS164962: MP:0002855 abnormal cochlear ganglion morphology
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 III Mouse 5726 Genes GS213077: Genes with suggestive difference in (PWD) vs (PB6F1 + B6PF1 + B6) comparison
Expand Tier I Human GO 68 Genes GS204815: GO:0005902 microvillus
Expand Tier I Mouse GO 3614 Genes GS180229: GO:0005886 plasma membrane
Expand Tier I Mouse MP 6 Genes GS168671: MP:0004578 abnormal cochlear hair bundle tip links morphology
Expand Tier I Mouse GO 364 Genes GS183891: GO:0002009 morphogenesis of an epithelium
Expand Tier I Mouse 3395 Genes GS127929: Medulla - Allen Mouse Brain Atlas
Expand Tier I Mouse GO 1041 Genes GS184451: GO:0044421 extracellular region part
Expand Tier I Mouse MP 495 Genes GS166123: MP:0002102 abnormal ear morphology
Expand Tier I Mouse MP 52 Genes GS169760: MP:0004763 absent brainstem auditory evoked potential
Expand Tier I Human GO 238 Genes GS196129: GO:0005929 cilium
Expand Tier I Mouse GO 1825 Genes GS193270: GO:0005576 extracellular region
Expand Tier I Mouse GO 2138 Genes GS186067: GO:0050877 neurological system process
Expand Tier I Mouse MP 14 Genes GS165668: MP:0004524 short cochlear hair cell stereocilia
Expand Tier I Human GO 3934 Genes GS198323: GO:0046872 metal ion binding
Expand Tier I Mouse GO 2498 Genes GS193018: GO:0003008 system process
Expand Tier I Mouse GO 197 Genes GS184011: GO:0030031 cell projection assembly
Expand Tier I Mouse GO 32 Genes GS186956: GO:0050982 detection of mechanical stimulus
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Mouse GO 2872 Genes GS178360: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Human 622 Genes GS219702: http://www.broadinstitute.org/gsea/msigdb/cards/INTRACELLULAR_NON_MEMBRANE_BOUND_ORGANELLE
Expand Tier I Mouse 536 Genes GS135339: atherosclerosis 17 (Ath17, Published QTL Chr 10)
Expand Tier I Mouse GO 491 Genes GS193293: GO:0000904 cell morphogenesis involved in differentiation
Expand Tier I Human 607 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Mouse GO 32 Genes GS188800: GO:0042491 auditory receptor cell differentiation
Expand Tier I Mouse MP 248 Genes GS166029: MP:0000960 abnormal sensory ganglion morphology
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Mouse DRG 85 Genes provisional GS86899: Table S1: Morphine regulation of gene expression in the LC in WT, AC1 KO, and AC8 KO Genes Significantly Regulated by Morphine in AC1 KO [DRG]
Expand Tier I Mouse 569 Genes GS135500: brain size control 1 (Bsc1, Published QTL Chr 10)
Expand Tier I Human 388 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Mouse GO 226 Genes GS181262: GO:0048562 embryonic organ morphogenesis
Expand Tier I Mouse GO 82 Genes GS183617: GO:0008344 adult locomotory behavior
Expand Tier I Mouse MP 51 Genes GS164273: MP:0000043 organ of Corti degeneration
Expand Tier I Human GO 75 Genes GS204969: GO:0050905 neuromuscular process
Expand Tier I Mouse MP 56 Genes GS163980: MP:0006089 abnormal vestibular saccule morphology
Expand Tier I Human 442 Genes GS176801: HP:0001263 Global developmental delay
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 Mouse 514 Genes GS135247: adiposity 15 (Adip15, Published QTL Chr 10)
Expand Tier I Mouse 545 Genes GS136099: long bones 9 (Lbn9, Published QTL Chr 10)
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Mouse GO 98 Genes GS181416: GO:0060271 cilium morphogenesis
Expand Tier II Mouse 312 Genes GS35420: Cerebellum Gene expression correlates of Zero Maze - Latency to enter an open quadrant in Females & Males BXD
Expand Tier I Mouse 550 Genes GS135327: arthropathy in MRL and DBA/1 mice 1 (Artmd1, Published QTL Chr 10)
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Human CTD 239 Genes GS122047: Ethylnitrosourea interacting genes (MeSH:D005038) in CTD
Expand Tier I Mouse GO 28 Genes GS181643: GO:0032421 stereocilium bundle
Expand Tier I Human GO 5436 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Mouse GO 2876 Genes GS182474: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier I Mouse MP 143 Genes GS169847: MP:0004399 abnormal cochlear outer hair cell morphology
Expand Tier I Mouse GO 50 Genes GS180534: GO:0050885 neuromuscular process controlling balance
Expand Tier I Mouse MP 710 Genes GS167922: MP:0000959 abnormal somatic sensory system morphology
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 Human GO 23 Genes GS198432: GO:0032420 stereocilium
Expand Tier I Mouse MP 162 Genes GS169277: MP:0001081 abnormal cranial ganglia morphology
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human 158 Genes GS171900: HP:0011452 Functional abnormality of the middle ear
Expand Tier I Mouse MP 14488 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 66 Genes GS173753: HP:0000510 Retinitis pigmentosa
Expand Tier I Mouse GO 3605 Genes GS190682: GO:0007275 multicellular organismal development
Expand Tier I Mouse MP 98 Genes GS165787: MP:0001522 impaired swimming
Expand Tier I Mouse GO 45 Genes GS185984: GO:0001750 photoreceptor outer segment
Expand Tier I Human 96 Genes GS176616: HP:0000662 Night blindness
Expand Tier I Human GO 1097 Genes GS201255: GO:0044421 extracellular region part
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 Human GO 668 Genes GS197076: GO:0005509 calcium ion binding
Expand Tier I Mouse GO 1550 Genes GS192290: GO:0007600 sensory perception
Expand Tier I Mouse GO 304 Genes GS187352: GO:0016337 cell-cell adhesion
Expand Tier I Mouse MP 1672 Genes GS165260: MP:0001392 abnormal locomotor behavior
Expand Tier I Mouse GO 165 Genes GS185499: GO:0007626 locomotory behavior
Expand Tier I Mouse MP 12 Genes GS165679: MP:0004529 decreased outer hair cell stereocilia number
Expand Human 622 Genes GS219997: http://www.broadinstitute.org/gsea/msigdb/cards/INTRACELLULAR_NON_MEMBRANE_BOUND_ORGANELLE
Expand Tier I Mouse MP 115 Genes GS169841: MP:0004393 abnormal cochlear inner hair cell morphology
Expand Tier I Mouse GO 20 Genes GS185854: GO:0001964 startle response
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 49 Genes GS164450: MP:0005191 head tilt
Expand Tier I Human GO 1236 Genes GS202899: GO:0050877 neurological system process
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 3375 Genes GS127927: Hypothalamus - Allen Mouse Brain Atlas
Expand Tier I Human GO 2139 Genes GS210214: GO:0005576 extracellular region
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Mouse MP 250 Genes GS168871: MP:0004738 abnormal brainstem auditory evoked potential
Expand Tier I Human CTD 64 Genes GS122390: Indinavir interacting genes (MeSH:D019469) in CTD