Gene Details



Pcdh15 and homologs in 5 species are found in 449 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.
GS185131: GO:0044699 single-organism process
GS168433: MP:0002980 abnormal postural reflex
GS167803: MP:0005307 head tossing
GS135258: anti-erythrocyte autoantibody modifier 3 (Aem3, Published QTL Chr 10)
GS135860: femur breaking strength 3 (Fembrs3, Published QTL Chr 10)
GS193051: GO:0051606 detection of stimulus
GS191625: GO:0040007 growth
GS188267: GO:0035058 nonmotile primary cilium assembly
GS174979: HP:0011061 Abnormality of dental structure
GS181012: GO:0007423 sensory organ development
GS165022: MP:0002857 cochlear ganglion degeneration
GS125369: Lamivudine interacting genes (MeSH:D019259) in CTD
GS35852: Striatum Gene expression correlates of Cocaine CPP - difference in time spent relative to baseline drug exposure in Males BXD
GS167764: MP:0004491 abnormal orientation of outer hair cell stereociliary bundles
GS136052: IGF-1 serum levels 2 (Igf1sl2, Published QTL Chr 10)
GS125368: Saquinavir interacting genes (MeSH:D019258) in CTD
GS171596: HP:0000164 Abnormality of the teeth
GS210482: GO:0007605 sensory perception of sound
GS166797: MP:0003143 enlarged otoliths
GS195976: GO:0007155 cell adhesion
GS203972: GO:0005615 extracellular space
GS136165: leishmaniasis resistance 19 (Lmr19, Published QTL Chr 10)
GS135790: epilepsy 3 (El3, Published QTL Chr 10)
GS171801: HP:0008527 Congenital sensorineural hearing impairment
GS177404: GO:0005737 cytoplasm
GS177265: GO:0048731 system development
GS201251: GO:0044424 intracellular part
GS135751: experimental allergic encephalomyelitis susceptibility 17 (Eae17, Published QTL Chr 10)
GS164837: MP:0006359 absent startle reflex
GS178359: GO:0071840 cellular component organization or biogenesis
GS210485: GO:0007601 visual perception
GS188142: GO:0048856 anatomical structure development
GS34463: Whole Brain Gene expression correlates of Novel environment locomotion (activity beam breaks) 15-30 min in the periphery in BXD Males
GS168066: MP:0002622 abnormal cochlear hair cell morphology
GS136910: vertebral morphology and mechanical traits 15 (Vmmt15, Published QTL Chr 10)
GS165461: MP:0001525 impaired balance
GS168293: MP:0004742 abnormal vestibular system physiology
GS178357: GO:0071842 cellular component organization at cellular level
GS166660: MP:0001731 abnormal postnatal growth
GS166905: MP:0001486 abnormal startle reflex
GS205500: GO:0071944 cell periphery
GS198664: GO:0043954 cellular component maintenance
GS173812: HP:0000738 Hallucinations
GS179236: GO:0048699 generation of neurons
GS176203: HP:0000478 Abnormality of the eye
GS127931: Olfactory bulb - Allen Mouse Brain Atlas
GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
GS178730: GO:0030534 adult behavior
GS188757: GO:0009887 organ morphogenesis
GS168674: MP:0002895 abnormal otolithic membrane morphology
GS175492: HP:0000512 Abnormal electroretinogram
GS179362: GO:0005929 cilium
GS165256: MP:0001395 bidirectional circling
GS165261: MP:0001393 ataxia
GS135323: apomorphine stress induced climbing 3 (Apsic3, Published QTL Chr 10)
GS175390: HP:0011007 Age of onset
GS196808: GO:0032501 multicellular organismal process
GS171708: HP:0000359 Abnormality of the inner ear
GS186744: GO:0043226 organelle
GS136631: small effect CIA locus 5 (Secia5, Published QTL Chr 10)
GS182835: GO:0005622 intracellular
GS189224: GO:0007610 behavior
GS127934: Retrohippocampal region - Allen Mouse Brain Atlas
GS164347: MP:0006334 abnormal susceptibility to hearing loss
GS184448: GO:0044425 membrane part
GS192628: GO:0048666 neuron development
GS194307: GO:0016043 cellular component organization
GS206742: GO:0043167 ion binding
GS175500: HP:0000517 Abnormality of the lens
GS174994: HP:0002059 Cerebral atrophy
GS164346: MP:0006335 abnormal hearing electrophysiology
GS175414: HP:0008619 Bilateral sensorineural hearing impairment
GS186963: GO:0045494 photoreceptor cell maintenance
GS197327: GO:0050885 neuromuscular process controlling balance
GS191212: GO:0009605 response to external stimulus
GS175528: HP:0000007 Autosomal recessive inheritance
GS181473: GO:0005488 binding
GS175526: HP:0000005 Mode of inheritance
GS180036: GO:0032501 multicellular organismal process
GS187237: GO:0030182 neuron differentiation
GS207616: GO:0016020 membrane
GS163601: MP:0002089 abnormal postnatal growth/weight/body size
GS183900: GO:0009582 detection of abiotic stimulus
GS164023: MP:0001961 abnormal reflex
GS188110: GO:0050905 neuromuscular process
GS167119: MP:0004577 abnormal cochlear hair cell inter-stereocilial links morphology
GS165527: MP:0005378 growth/size phenotype
GS175529: HP:0000001 All
GS177976: GO:0035264 multicellular organism growth
GS188813: GO:0045202 synapse
GS127938: Striatum - Allen Mouse Brain Atlas
GS163801: MP:0003637 cochlear ganglion hypoplasia
GS205674: GO:0045202 synapse
GS186740: GO:0043229 intracellular organelle
GS173329: HP:0000682 Abnormality of dental enamel
GS188314: GO:0007156 homophilic cell adhesion
GS187955: GO:0005902 microvillus
GS208012: GO:0044464 cell part
GS165664: MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles
GS187113: GO:0005615 extracellular space
GS178598: GO:0072372 primary cilium
GS201252: GO:0044425 membrane part
GS136778: systolic blood pressure 1 (Sysbp1, Published QTL Chr 10)
GS188763: GO:0009888 tissue development
GS179210: GO:0007155 cell adhesion
GS193043: GO:0050954 sensory perception of mechanical stimulus
GS185005: GO:0050974 detection of mechanical stimulus involved in sensory perception
GS172732: HP:0001751 Vestibular dysfunction
GS171791: HP:0000370 Abnormality of the middle ear
GS167020: MP:0003956 abnormal body size
GS127928: Lateral septal complex - Allen Mouse Brain Atlas
GS34462: Whole Brain Gene expression correlates of Novel environment locomotion (activity beam breaks) 15-30 min in the periphery in Males BXD
GS199635: GO:0005622 intracellular
GS206917: GO:0031513 nonmotile primary cilium
GS121976: Zidovudine interacting genes (MeSH:D015215) in CTD
GS181873: GO:0043954 cellular component maintenance
GS192719: GO:0060013 righting reflex
GS180679: GO:0009628 response to abiotic stimulus
GS127935: Striatum dorsal region - Allen Mouse Brain Atlas
GS165390: MP:0003224 neuron degeneration
GS36760: Hippocampus Gene expression correlates of Vocalization Threshold - shock intensity (mA) in Males BXD
GS167233: MP:0004300 abnormal organ of Corti supporting cell morphology
GS135635: collagen induced arthritis QTL 8 (Cia8, Published QTL Chr 10)
GS171968: HP:0000405 Conductive hearing impairment
GS196941: GO:0008150 biological_process
GS14908: Nicotine Abstinence Genes found in Genome-wide Association Studies (GWAS)
GS170347: MP:0004748 increased susceptibility to age-related hearing loss
GS176289: HP:0002120 Cerebral cortical atrophy
GS135699: directional asymmetry QTL 6 (Daq6, Published QTL Chr 10)
GS190893: GO:0030154 cell differentiation
GS187648: GO:0048729 tissue morphogenesis
GS197009: GO:0005886 plasma membrane
GS201256: GO:0044422 organelle part
GS165873: MP:0004404 cochlear outer hair cell degeneration
GS193537: GO:0007605 sensory perception of sound
GS183899: GO:0009581 detection of external stimulus
GS135438: bone mineral density 38 (Bmd38, Published QTL Chr 10)
GS163827: MP:0011062 abnormal outer hair cell kinocilium morphology
GS173147: HP:0011283 Abnormality of the metencephalon
GS136941: vertebral trabecular bone trait 9 (Vtbt9, Published QTL Chr 10)
GS187160: GO:0044707 single-multicellular organism process
GS163829: MP:0011060 abnormal kinocilium morphology
GS190682: GO:0007275 multicellular organismal development
GS165666: MP:0004523 decreased cochlear hair cell stereocilia number
GS165787: MP:0001522 impaired swimming
GS185984: GO:0001750 photoreceptor outer segment
GS195352: GO:0072372 primary cilium
GS176616: HP:0000662 Night blindness
GS174247: HP:0000539 Abnormality of refraction
GS200151: GO:0022610 biological adhesion
GS167643: MP:0000034 abnormal vestibule morphology
GS201255: GO:0044421 extracellular region part
GS171274: HP:0100543 Cognitive impairment
GS168215: MP:0001967 deafness
GS188826: GO:0022008 neurogenesis
GS175981: HP:0000163 Abnormality of the oral cavity
GS199272: GO:0043232 intracellular non-membrane-bounded organelle
GS167452: MP:0004532 abnormal inner hair cell stereociliary bundle morphology
GS171848: HP:0000598 Abnormality of the ear
GS197076: GO:0005509 calcium ion binding
GS192290: GO:0007600 sensory perception
GS204021: GO:0044707 single-multicellular organism process
GS187352: GO:0016337 cell-cell adhesion
GS26241: Hippocampus Gene expression correlates of Mechanical Nociception - Tail Clip Test in Females BXD
GS165260: MP:0001392 abnormal locomotor behavior
GS184629: GO:0005515 protein binding
GS185499: GO:0007626 locomotory behavior
GS163498: MP:0003308 abnormal cochlear sensory epithelium morphology
GS165679: MP:0004529 decreased outer hair cell stereocilia number
GS169841: MP:0004393 abnormal cochlear inner hair cell morphology
GS135614: circulating hormone level QTL 6 (Chlq6, Published QTL Chr 10)
GS169967: MP:0001408 stereotypic behavior
GS185854: GO:0001964 startle response
GS165538: MP:0005377 hearing/vestibular/ear phenotype
GS166743: MP:0002229 neurodegeneration
GS186488: GO:0048513 organ development
GS165397: MP:0001265 decreased body size
GS168218: MP:0001963 abnormal hearing physiology
GS164450: MP:0005191 head tilt
GS169095: MP:0004924 abnormal behavior
GS202899: GO:0050877 neurological system process
GS164570: MP:0003878 abnormal ear physiology
GS165255: MP:0001394 circling
GS167164: MP:0004527 abnormal outer hair cell stereociliary bundle morphology
GS172030: HP:0000365 Hearing impairment
GS84241: alcohol preference (Published QTL, Chr 10)
GS127927: Hypothalamus - Allen Mouse Brain Atlas
GS170965: HP:0000153 Abnormality of the mouth
GS181215: GO:0007399 nervous system development
GS210214: GO:0005576 extracellular region
GS203594: GO:0043226 organelle
GS168871: MP:0004738 abnormal brainstem auditory evoked potential
GS122390: Indinavir interacting genes (MeSH:D019469) in CTD
GS192629: GO:0048667 cell morphogenesis involved in neuron differentiation
GS136397: organ weight 6 (Org6, Published QTL Chr 10)
GS171168: HP:0000234 Abnormality of the head
GS136076: insulin QTL 9 (Insq9, Published QTL Chr 10)
GS169793: MP:0004425 abnormal otolith organ morphology
GS203824: GO:0045494 photoreceptor cell maintenance
GS180171: GO:0060122 inner ear receptor stereocilium organization
GS190034: GO:0031513 nonmotile primary cilium
GS177398: GO:0010927 cellular component assembly involved in morphogenesis
GS209960: GO:0003008 system process
GS163063: MP:0000042 abnormal organ of Corti morphology
GS175668: HP:0007369 Atrophy/Degeneration affecting the cerebrum
GS168958: MP:0003492 abnormal involuntary movement
GS180716: GO:0042472 inner ear morphogenesis
GS181102: GO:0043228 non-membrane-bounded organelle
GS193540: GO:0007601 visual perception
GS165463: MP:0001523 impaired righting response
GS179560: GO:0048839 inner ear development
GS164742: MP:0001732 postnatal growth retardation
GS167765: MP:0004492 abnormal orientation of inner hair cell stereociliary bundles
GS182404: GO:0031224 intrinsic to membrane
GS127924: Cerebral cortex - Allen Mouse Brain Atlas
GS127925: Hippocampal formation - Allen Mouse Brain Atlas
GS174131: HP:0002011 Abnormality of the central nervous system
GS194087: GO:0003674 molecular_function
GS204214: GO:0016337 cell-cell adhesion
GS135326: age related thymic involution 2 (Arti2, Published QTL Chr 10)
GS170320: MP:0004813 absent linear vestibular evoked potential
GS177356: GO:0003674 molecular_function
GS207615: GO:0016021 integral to membrane
GS163227: MP:0003313 abnormal locomotor activation
GS203590: GO:0043229 intracellular organelle
GS180001: GO:0048646 anatomical structure formation involved in morphogenesis
GS135585: cholesterol absorption 2 (Chab2, Published QTL Chr 10)
GS171631: HP:0008051 Abnormality of the retinal pigment epithelium
GS176245: HP:0011443 Abnormality of coordination
GS176610: HP:0003593 Infantile onset
GS164033: MP:0004812 abnormal linear vestibular evoked potential
GS165663: MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology
GS192471: GO:0048869 cellular developmental process
GS165985: MP:0000965 abnormal sensory neuron morphology
GS187246: GO:0060088 auditory receptor cell stereocilium organization
GS165114: MP:0004426 abnormal cochlear labyrinth morphology
GS171832: HP:0000118 Phenotypic abnormality
GS191056: GO:0050973 detection of mechanical stimulus involved in equilibrioception
GS189304: GO:0002093 auditory receptor cell morphogenesis
GS189630: GO:0060117 auditory receptor cell development
GS185850: GO:0060113 inner ear receptor cell differentiation
GS127937: Striatum-like amygdalar nuclei - Allen Mouse Brain Atlas
GS165544: MP:0004362 cochlear hair cell degeneration
GS164724: MP:0001516 abnormal motor coordination/ balance
GS136151: "lupus in MRL and B6 F2 cross, QTL 4" (Lmb4, Published QTL Chr 10)
GS185506: GO:0007628 adult walking behavior
GS36158: Neocortex Gene expression correlates of Locomotor response of 10 mg/kg MDMA injected on Day 2 in Females BXD
GS127936: Striatum ventral region - Allen Mouse Brain Atlas
GS165391: MP:0000972 abnormal mechanoreceptor morphology
GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
GS168956: MP:0003491 abnormal voluntary movement
GS190714: GO:0016020 membrane
GS136675: skull morphology 14 (Skull14, Published QTL Chr 10)
GS191552: GO:0042995 cell projection
GS135606: circulating hormone level QTL 15 (Chlq15, Published QTL Chr 10)
GS195214: GO:0009987 cellular process
GS184452: GO:0044422 organelle part
GS198431: GO:0032421 stereocilium bundle
GS180034: GO:0032502 developmental process
GS195112: GO:0071840 cellular component organization or biogenesis
GS176586: HP:0001270 Motor delay
GS162895: MP:0003986 small cochlear ganglion
GS170740: MP:0003825 abnormal pillar cell morphology
GS35418: Neocortex Gene expression correlates of Zero Maze - Latency to enter an open quadrant in Females & Males BXD
GS187166: GO:0044708 single-organism behavior
GS175714: HP:0011389 Functional abnormality of the inner ear
GS163316: MP:0000035 abnormal membranous labyrinth morphology
GS188268: GO:0030029 actin filament-based process
GS176115: HP:0000540 Hypermetropia
GS198263: GO:0005488 binding
GS171512: HP:0007703 Abnormal retinal pigmentation
GS175169: HP:0001317 Abnormality of the cerebellum
GS192918: GO:0050896 response to stimulus
GS170971: HP:0000407 Sensorineural hearing impairment
GS167140: MP:0003169 abnormal scala media morphology
GS180713: GO:0042471 ear morphogenesis
GS165804: MP:0002862 altered righting response
GS184782: GO:0009612 response to mechanical stimulus
GS127939: Thalamus - Allen Mouse Brain Atlas
GS193044: GO:0050957 equilibrioception
GS172353: HP:0004329 Abnormality of the posterior segment of the eye
GS181644: GO:0032420 stereocilium
GS163724: MP:0000436 abnormal head movements
GS14904: Genes Harboring Allelic Variants That Distinguish Successful vs Unsuccessful Nicotine Abstainers in at Least 2 Samples
GS188801: GO:0042490 mechanoreceptor differentiation
GS178975: GO:0022607 cellular component assembly
GS180164: GO:0008150 biological_process
GS179167: GO:0007015 actin filament organization
GS176333: HP:0007319 Morphological abnormality of the central nervous system
GS188287: GO:0048468 cell development
GS178355: GO:0071844 cellular component assembly at cellular level
GS34483: Whole Brain Gene expression correlates of Novel environment locomotion (activity beam breaks) 15-30 min in the periphery [Cocaine] in Males BXD
GS180237: GO:0032990 cell part morphogenesis
GS186562: GO:0009653 anatomical structure morphogenesis
GS188107: GO:0050906 detection of stimulus involved in sensory perception
GS188400: GO:0060004 reflex
GS205171: GO:0007156 homophilic cell adhesion
GS167666: MP:0000032 cochlear degeneration
GS127930: Midbrain - Allen Mouse Brain Atlas
GS127933: Pons - Allen Mouse Brain Atlas
GS173476: HP:0002311 Incoordination
GS209985: GO:0050957 equilibrioception
GS208482: GO:0042995 cell projection
GS165465: MP:0003633 abnormal nervous system physiology
GS193294: GO:0000902 cell morphogenesis
GS125506: Valproic Acid interacting genes (MeSH:D014635) in CTD
GS209987: GO:0050953 sensory perception of light stimulus
GS181684: GO:0042384 cilium assembly
GS136454: postnatal body weight growth 16 (Pbwg16, Published QTL Chr 10)
GS164220: MP:0002882 abnormal neuron morphology
GS163596: MP:0000026 abnormal inner ear morphology
GS201949: GO:0044699 single-organism process
GS179173: GO:0007010 cytoskeleton organization
GS188641: GO:0071944 cell periphery
GS165766: MP:0004303 abnormal Hensen cell morphology
GS135645: cardiac modifier of nmd 2 (Cmn2, Published QTL Chr 10)
GS178461: GO:0009987 cellular process
GS192041: GO:0043169 cation binding
GS165253: MP:0001399 hyperactivity
GS136079: juvenile cystic kidney modifier 1 (Jckm1, Published QTL Chr 10)
GS193268: GO:0005575 cellular_component
GS163828: MP:0011061 abnormal inner hair cell kinocilium morphology
GS193046: GO:0050953 sensory perception of light stimulus
GS127923: Cerebellum - Allen Mouse Brain Atlas
GS176817: HP:0011446 Abnormality of higher mental function
GS190713: GO:0016021 integral to membrane
GS180296: GO:0005509 calcium ion binding
GS182313: GO:0044085 cellular component biogenesis
GS192986: GO:0006996 organelle organization
GS163320: MP:0000031 abnormal cochlea morphology
GS187229: GO:0043583 ear development
GS163925: MP:0002894 abnormal otolith morphology
GS165466: MP:0003632 abnormal nervous system morphology
GS126989: Hydralazine interacting genes (MeSH:D006830) in CTD
GS169228: MP:0001406 abnormal gait
GS169758: MP:0004765 decreased brainstem auditory evoked potential
GS170964: HP:0000152 Abnormality of head and neck
GS175674: HP:0007360 Aplasia/Hypoplasia of the cerebellum
GS191106: GO:0044464 cell part
GS177570: GO:0016043 cellular component organization
GS192584: GO:0032989 cellular component morphogenesis
GS172031: HP:0000364 Hearing abnormality
GS181533: GO:0046872 metal ion binding
GS169795: MP:0004427 abnormal vestibular labyrinth morphology
GS184013: GO:0030036 actin cytoskeleton organization
GS165617: MP:0004398 cochlear inner hair cell degeneration
GS181267: GO:0048568 embryonic organ development
GS171453: HP:0003674 Onset
GS163226: MP:0003312 abnormal locomotor coordination
GS174378: HP:0000518 Cataract
GS209225: GO:0007600 sensory perception
GS202821: GO:0001750 photoreceptor outer segment
GS171277: HP:0100547 Abnormality of the forebrain
GS135360: B.burgdorferi-associated arthritis 18 (Bbaa18, Published QTL Chr 10)
GS185033: GO:0048598 embryonic morphogenesis
GS173146: HP:0011282 Abnormality of the hindbrain
GS183355: GO:0022610 biological adhesion
GS188136: GO:0048858 cell projection morphogenesis
GS135697: directional asymmetry QTL 4 (Daq4, Published QTL Chr 10)
GS35954: Hippocampus Gene expression correlates of Handling induced convulsion baseline in Males BXD
GS173589: HP:0008513 Bilateral conductive hearing impairment
GS208978: GO:0043169 cation binding
GS163068: MP:0000045 abnormal hair cell morphology
GS136122: life span 2 (Lifespan2, Published QTL Chr 10)
GS164126: MP:0001388 abnormal stationary movement
GS136154: limb length QTL 4 (Lmblgq4, Published QTL Chr 10)
GS164059: MP:0006325 impaired hearing
GS197892: GO:0043228 non-membrane-bounded organelle
GS184317: GO:0009790 embryo development
GS127926: Hippocampal region - Allen Mouse Brain Atlas
GS169828: MP:0005386 behavior/neurological phenotype
GS127932: Pallidum - Allen Mouse Brain Atlas
GS166244: MP:0002752 abnormal somatic nervous system morphology
GS135698: directional asymmetry QTL 5 (Daq5, Published QTL Chr 10)
GS189860: GO:0043167 ion binding
GS175525: HP:0000004 Onset and clinical course
GS174764: HP:0007367 Atrophy/Degeneration affecting the central nervous system
GS163803: MP:0003631 nervous system phenotype
GS136004: hepatocarcinogen resistance 2 (Hpcr2, Published QTL Chr 10)
GS192427: GO:0050910 detection of mechanical stimulus involved in sensory perception of sound
GS135312: aortic lesion size 1 (Aorls1, Published QTL Chr 10)
GS182820: GO:0060429 epithelium development
GS164962: MP:0002855 abnormal cochlear ganglion morphology
GS173991: HP:0000505 Visual impairment
GS169391: MP:0002066 abnormal motor capabilities/coordination/movement
GS169390: MP:0002067 abnormal sensory capabilities/reflexes/nociception
GS177031: HP:0011442 Abnormality of central motor function
GS172354: HP:0004328 Abnormality of the anterior segment of the eye
GS184010: GO:0030030 cell projection organization
GS174836: HP:0001098 Abnormality of the fundus
GS213077: Genes with suggestive difference in (PWD) vs (PB6F1 + B6PF1 + B6) comparison
GS204815: GO:0005902 microvillus
GS180229: GO:0005886 plasma membrane
GS168671: MP:0004578 abnormal cochlear hair bundle tip links morphology
GS183891: GO:0002009 morphogenesis of an epithelium
GS127929: Medulla - Allen Mouse Brain Atlas
GS184451: GO:0044421 extracellular region part
GS166123: MP:0002102 abnormal ear morphology
GS169760: MP:0004763 absent brainstem auditory evoked potential
GS196129: GO:0005929 cilium
GS193270: GO:0005576 extracellular region
GS186067: GO:0050877 neurological system process
GS165668: MP:0004524 short cochlear hair cell stereocilia
GS198323: GO:0046872 metal ion binding
GS193018: GO:0003008 system process
GS184011: GO:0030031 cell projection assembly
GS186956: GO:0050982 detection of mechanical stimulus
GS184447: GO:0044424 intracellular part
GS178360: GO:0071841 cellular component organization or biogenesis at cellular level
GS135339: atherosclerosis 17 (Ath17, Published QTL Chr 10)
GS193293: GO:0000904 cell morphogenesis involved in differentiation
GS175191: HP:0002060 Abnormality of the cerebrum
GS188800: GO:0042491 auditory receptor cell differentiation
GS166029: MP:0000960 abnormal sensory ganglion morphology
GS210212: GO:0005575 cellular_component
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] provisional
GS135500: brain size control 1 (Bsc1, Published QTL Chr 10)
GS176202: HP:0000479 Abnormality of the retina
GS181262: GO:0048562 embryonic organ morphogenesis
GS183617: GO:0008344 adult locomotory behavior
GS164273: MP:0000043 organ of Corti degeneration
GS204969: GO:0050905 neuromuscular process
GS163980: MP:0006089 abnormal vestibular saccule morphology
GS176801: HP:0001263 Global developmental delay
GS174449: HP:0001123 Visual field defect
GS172195: HP:0000504 Abnormality of vision
GS135247: adiposity 15 (Adip15, Published QTL Chr 10)
GS136099: long bones 9 (Lbn9, Published QTL Chr 10)
GS174500: HP:0000707 Abnormality of the nervous system
GS181416: GO:0060271 cilium morphogenesis
GS35420: Cerebellum Gene expression correlates of Zero Maze - Latency to enter an open quadrant in Females & Males BXD
GS135327: arthropathy in MRL and DBA/1 mice 1 (Artmd1, Published QTL Chr 10)
GS182834: GO:0005623 cell
GS122047: Ethylnitrosourea interacting genes (MeSH:D005038) in CTD
GS181643: GO:0032421 stereocilium bundle
GS199201: GO:0031224 intrinsic to membrane
GS182474: GO:0043232 intracellular non-membrane-bounded organelle
GS169847: MP:0004399 abnormal cochlear outer hair cell morphology
GS180534: GO:0050885 neuromuscular process controlling balance
GS167922: MP:0000959 abnormal somatic sensory system morphology
GS209984: GO:0050954 sensory perception of mechanical stimulus
GS179162: GO:0060119 inner ear receptor cell development
GS198432: GO:0032420 stereocilium
GS169277: MP:0001081 abnormal cranial ganglia morphology
GS199634: GO:0005623 cell
GS171900: HP:0011452 Functional abnormality of the middle ear
GS164136: MP:0000001 mammalian phenotype
GS176613: HP:0000271 Abnormality of the face
GS173753: HP:0000510 Retinitis pigmentosa