Gene Details



USH1G and homologs in 4 species are found in 336 GeneSets:


- Entrez   - Ensembl   - GeneNetwork   - STRING   - Allen Brain Atlas   - Comparative Toxicogenomics Database  

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier I Mouse GO 7755 Genes GS185131: GO:0044699 single-organism process
Expand Tier I Mouse 1003 Genes GS136433: pulmonary adenoma susceptibility 5a (Pas5a, Published QTL Chr 11)
Expand Tier I Mouse MP 50 Genes GS167803: MP:0005307 head tossing
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 MP 18 Genes GS166834: MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology
Expand Tier I Mouse GO 3706 Genes GS188641: GO:0071944 cell periphery
Expand Tier I Mouse 579 Genes GS129172: pregnancy QTL 2 (Pregq2 Published QTL Chr 11)
Expand Tier I Mouse MP 13 Genes GS166126: MP:0004412 abnormal cochlear microphonics
Expand Tier I Mouse MP 5 Genes GS168036: MP:0004466 short cochlear outer hair cells
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Human 154 Genes GS174979: HP:0011061 Abnormality of dental structure
Expand Tier I Mouse MP 466 Genes GS165253: MP:0001399 hyperactivity
Expand Tier I Mouse GO 454 Genes GS181012: GO:0007423 sensory organ development
Expand Tier I Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Mouse 692 Genes GS135389: body growth early QTL 10 (Bgeq10, Published QTL Chr 11)
Expand Tier I Mouse GO 123 Genes GS193046: GO:0050953 sensory perception of light stimulus
Expand Tier I Human GO 566 Genes GS194646: GO:0042803 protein homodimerization activity
Expand Tier I Human 379 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Human GO 2661 Genes GS207797: GO:0030154 cell differentiation
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 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 Human GO 4024 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human 639 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Mouse MP 13 Genes GS164341: MP:0006332 abnormal cochlear potential
Expand Tier I Mouse 1003 Genes GS135818: ethanol induced thermoregulation 4 (Ethm4, Published QTL Chr 11)
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 1046 Genes GS135496: brain weight QTL 1 (Brwq1, Published QTL Chr 11)
Expand Tier I Mouse MP 54 Genes GS166643: MP:0010055 abnormal sensory neuron physiology
Expand Tier I Mouse MP 39 Genes GS164569: MP:0003879 abnormal hair cell physiology
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 MP 17 Genes GS165666: MP:0004523 decreased cochlear hair cell stereocilia number
Expand Tier I Mouse GO 8406 Genes GS177404: GO:0005737 cytoplasm
Expand Tier I Mouse GO 3493 Genes GS177570: GO:0016043 cellular component organization
Expand Tier I Mouse GO 3080 Genes GS177265: GO:0048731 system development
Expand Tier I Human GO 1789 Genes GS208893: GO:0005856 cytoskeleton
Expand Tier I Human GO 95 Genes GS197513: GO:0042472 inner ear morphogenesis
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Mouse 1046 Genes GS135528: castaneus 10 week body weight 3 (C10bw3, Published QTL Chr 11)
Expand Tier I Mouse MP 98 Genes GS165787: MP:0001522 impaired swimming
Expand Tier I Human 592 Genes GS172031: HP:0000364 Hearing abnormality
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 MP 189 Genes GS168193: MP:0000966 decreased sensory neuron number
Expand Tier I Human 96 Genes GS176616: HP:0000662 Night blindness
Expand Tier I Mouse GO 3597 Genes GS188142: GO:0048856 anatomical structure development
Expand Tier I Mouse MP 173 Genes GS168066: MP:0002622 abnormal cochlear hair cell morphology
Expand Tier I Mouse MP 90 Genes GS169795: MP:0004427 abnormal vestibular labyrinth morphology
Expand Tier I Human 189 Genes GS174247: HP:0000539 Abnormality of refraction
Expand Tier I Mouse MP 86 Genes GS167643: MP:0000034 abnormal vestibule morphology
Expand Tier I Mouse MP 58 Genes GS168293: MP:0004742 abnormal vestibular system physiology
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 986 Genes GS204095: GO:0030182 neuron differentiation
Expand Tier I Mouse GO 348 Genes GS181267: GO:0048568 embryonic organ development
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 Human GO 3125 Genes GS199272: GO:0043232 intracellular non-membrane-bounded organelle
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 801 Genes GS136780: seizure susceptibility 3 (Szs3, Published QTL Chr 11)
Expand Tier I Mouse MP 814 Genes GS163226: MP:0003312 abnormal locomotor coordination
Expand Tier I Human GO 4371 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Human 344 Genes GS174378: HP:0000518 Cataract
Expand Tier I Mouse MP 7 Genes GS167450: MP:0004534 decreased inner hair cell stereocilia number
Expand Tier I Mouse GO 1550 Genes GS192290: GO:0007600 sensory perception
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 38 Genes GS198664: GO:0043954 cellular component maintenance
Expand Tier I Mouse MP 1672 Genes GS165260: MP:0001392 abnormal locomotor behavior
Expand Tier I Mouse GO 6204 Genes GS184629: GO:0005515 protein binding
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 Mouse GO 500 Genes GS185033: GO:0048598 embryonic morphogenesis
Expand Tier I Mouse MP 181 Genes GS163498: MP:0003308 abnormal cochlear sensory epithelium morphology
Expand Tier I Mouse MP 12 Genes GS165679: MP:0004529 decreased outer hair cell stereocilia number
Expand Tier I Human 50 Genes GS173812: HP:0000738 Hallucinations
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 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 858 Genes GS194645: GO:0042802 identical protein binding
Expand Tier I Mouse GO 912 Genes GS179236: GO:0048699 generation of neurons
Expand Tier I Mouse MP 295 Genes GS169967: MP:0001408 stereotypic behavior
Expand Tier I Mouse 697 Genes GS135386: berghei resistance locus 2 (Berr2, Published QTL Chr 11)
Expand Tier I Human GO 216 Genes GS198051: GO:0048562 embryonic organ morphogenesis
Expand Tier I Mouse MP 6 Genes GS167405: MP:0004531 short outer hair cell stereocilia
Expand Tier I Human 1 Genes GS176230: HP:0010939 Abnormality of the nasal bone
Expand Tier I Human GO 899 Genes GS201125: GO:0009790 embryo development
Expand Tier I Mouse MP 639 Genes GS164032: MP:0004811 abnormal neuron physiology
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 344 Genes GS168218: MP:0001963 abnormal hearing physiology
Expand Tier I Mouse MP 180 Genes GS163068: MP:0000045 abnormal hair cell morphology
Expand Tier I Mouse MP 13 Genes GS164027: MP:0004814 reduced linear vestibular evoked potential
Expand Tier I Mouse MP 3543 Genes GS169095: MP:0004924 abnormal behavior
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 1236 Genes GS202899: GO:0050877 neurological system process
Expand Tier I Mouse 1060 Genes GS135973: wound healing/regeneration 10 (Heal10, Published QTL Chr 11)
Expand Tier I Mouse MP 400 Genes GS164570: MP:0003878 abnormal ear physiology
Expand Tier I Mouse MP 183 Genes GS165255: MP:0001394 circling
Expand Tier I Mouse MP 54 Genes GS167164: MP:0004527 abnormal outer hair cell stereociliary bundle morphology
Expand Tier I Human 578 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Mouse GO 758 Genes GS188757: GO:0009887 organ morphogenesis
Expand Tier I Mouse 1060 Genes GS135353: Alzheimer's disease modifier 5 (Azdm5, Published QTL Chr 11)
Expand Tier I Human GO 4567 Genes GS196806: GO:0032502 developmental process
Expand Tier I Mouse MP 262 Genes GS164126: MP:0001388 abnormal stationary movement
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human 124 Genes GS175492: HP:0000512 Abnormal electroretinogram
Expand Tier I Mouse GO 1398 Genes GS181215: GO:0007399 nervous system development
Expand Tier I Mouse 715 Genes GS135815: ethanol induced ataxia 10 (Etax10, Published QTL Chr 11)
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 Mouse 735 Genes GS135276: "alcohol preference locus 20, female specific" (Alcp20, Published QTL Chr 11)
Expand Tier I Mouse MP 30 Genes GS165256: MP:0001395 bidirectional circling
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 Mouse MP 8 Genes GS166132: MP:0004413 absent cochlear microphonics
Expand Tier I Mouse MP 29 Genes GS165729: MP:0002730 head shaking
Expand Tier I Human GO 3125 Genes GS197892: GO:0043228 non-membrane-bounded organelle
Expand Tier I Human GO 6769 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Mouse MP 63 Genes GS169793: MP:0004425 abnormal otolith organ morphology
Expand Tier I Human GO 25 Genes GS203824: GO:0045494 photoreceptor cell maintenance
Expand Tier I Mouse GO 903 Genes GS184317: GO:0009790 embryo development
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 Human GO 1693 Genes GS209960: GO:0003008 system process
Expand Tier I Mouse MP 22 Genes GS165864: MP:0004405 absent cochlear hair cells
Expand Tier I Mouse MP 3543 Genes GS169828: MP:0005386 behavior/neurological phenotype
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 11364 Genes GS182835: GO:0005622 intracellular
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 700 Genes GS136632: small effect CIA locus 6 (Secia6, Published QTL Chr 11)
Expand Tier I Mouse 1046 Genes GS136952: weight gain in high growth mice 7 (Wg7, Published QTL Chr 11)
Expand Tier I Mouse GO 159 Genes GS179560: GO:0048839 inner ear development
Expand Tier I Mouse 714 Genes GS135555: CD8 memory T cell subset 4 (Cd8mts4, Published QTL Chr 11)
Expand Tier I Mouse 1046 Genes GS135812: estradiol regulated response QTL 3 (Estq3, Published QTL Chr 11)
Expand Tier I Mouse 792 Genes GS136220: mandible length 12 (Manln12, Published QTL Chr 11)
Expand Tier I Mouse MP 983 Genes GS166244: MP:0002752 abnormal somatic nervous system morphology
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 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human GO 2050 Genes GS203406: GO:0009653 anatomical structure morphogenesis
Expand Tier I Human GO 183 Genes GS204087: GO:0043583 ear development
Expand Tier I Mouse MP 15 Genes GS164584: MP:0004331 vestibular saccular macula degeneration
Expand Tier I Mouse MP 56 Genes GS164345: MP:0006336 abnormal otoacoustic response
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 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 403 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Mouse GO 1466 Genes GS180001: GO:0048646 anatomical structure formation involved in morphogenesis
Expand Tier I Mouse 767 Genes GS135792: epilepsy 6 (El6, Published QTL Chr 11)
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 II Mouse 792 Genes GS84255: alcohol preference locus (Published QTL, Chr 11)
Expand Tier I Mouse 1003 Genes GS135678: compensatory renal hypertrophy QTL 1 (Crhq1, Published QTL Chr 11)
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 Human 202 Genes GS174764: HP:0007367 Atrophy/Degeneration affecting the central nervous system
Expand Tier I Mouse MP 487 Genes GS167105: MP:0008948 decreased neuron number
Expand Tier I Human GO 4097 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Mouse MP 211 Genes GS165114: MP:0004426 abnormal cochlear labyrinth morphology
Expand Tier I Mouse MP 3716 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier I Human 1 Genes GS171027: HP:0010940 Aplasia/Hypoplasia of the nasal bone
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Mouse MP 32 Genes GS164571: MP:0004432 abnormal cochlear hair cell physiology
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 II Mouse 730 Genes GS83981: cocaine related behavior 12 (Cocrb12, Published QTL, Chr 11)
Expand Tier I Mouse MP 268 Genes GS164346: MP:0006335 abnormal hearing electrophysiology
Expand Tier I Human GO 39 Genes GS202686: GO:0060113 inner ear receptor cell differentiation
Expand Tier I Mouse 705 Genes GS135906: gonadal fat pad weight QTL 1 (Gfpq1, Published QTL Chr 11)
Expand Tier I Mouse GO 24 Genes GS186963: GO:0045494 photoreceptor cell maintenance
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 MP 1013 Genes GS164724: MP:0001516 abnormal motor coordination/ balance
Expand Tier I Human 364 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Mouse 692 Genes GS136896: visual placing (Vispl, Published QTL Chr 11)
Expand Tier I Mouse MP 2406 Genes GS169391: MP:0002066 abnormal motor capabilities/coordination/movement
Expand Tier I Mouse 705 Genes GS136357: novelty/stress induced locomotor activation 8 (Nsila8, Published QTL Chr 11)
Expand Tier I Human GO 45 Genes GS197327: GO:0050885 neuromuscular process controlling balance
Expand Tier I Human GO 45 Genes GS205662: GO:0042490 mechanoreceptor differentiation
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
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 Mouse MP 206 Genes GS165391: MP:0000972 abnormal mechanoreceptor morphology
Expand Tier I Human 544 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 472 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
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 580 Genes GS177903: GO:0042803 protein homodimerization activity
Expand Tier I Human 512 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Mouse 697 Genes GS136957: weight 5 (Wght5, Published QTL Chr 11)
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 Mouse MP 1825 Genes GS168956: MP:0003491 abnormal voluntary movement
Expand Tier I Mouse GO 8145 Genes GS190714: GO:0016020 membrane
Expand Tier I Human GO 7808 Genes GS207616: GO:0016020 membrane
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse GO 3614 Genes GS180229: GO:0005886 plasma membrane
Expand Tier I Human GO 1724 Genes GS198004: GO:0007399 nervous system development
Expand Tier I Mouse MP 6 Genes GS168671: MP:0004578 abnormal cochlear hair bundle tip links morphology
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 GO 113 Genes GS197510: GO:0042471 ear morphogenesis
Expand Tier I Mouse MP 7 Genes GS167448: MP:0004536 short inner hair cell stereocilia
Expand Tier I Mouse 1281 Genes GS129115: collagen induced arthritis 40 (Cia40 Published QTL Chr 11)
Expand Tier I Mouse 981 Genes GS136789: tail length QTL 8 (Tailq8, Published QTL Chr 11)
Expand Tier I Human GO 3513 Genes GS193991: GO:0048731 system development
Expand Tier I Mouse MP 10 Genes GS163543: MP:0004431 abnormal hair cell mechanoelectric transduction
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 MP 648 Genes GS164023: MP:0001961 abnormal reflex
Expand Tier I Mouse 697 Genes GS136244: methamphetamine response QTL 3 (Marq3, Published QTL Chr 11)
Expand Tier I Mouse 792 Genes GS136831: TNF-induced lethal shock susceptibility 2 (Tilss2, Published QTL Chr 11)
Expand Tier I Human 41 Genes GS176115: HP:0000540 Hypermetropia
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 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 Human 188 Genes GS171512: HP:0007703 Abnormal retinal pigmentation
Expand Tier I Mouse 981 Genes GS135755: experimental allergic encephalomyelitis susceptibility 22 (Eae22, Published QTL Chr 11)
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 416 Genes GS175169: HP:0001317 Abnormality of the cerebellum
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 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human 368 Genes GS170971: HP:0000407 Sensorineural hearing impairment
Expand Tier I Mouse MP 23 Genes GS167591: MP:0004330 abnormal vestibular saccular macula morphology
Expand Tier I Mouse GO 2498 Genes GS193018: GO:0003008 system process
Expand Tier I Mouse 792 Genes GS135341: atherosclerosis 19 (Ath19, Published QTL Chr 11)
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 71 Genes GS165854: MP:0004406 abnormal cochlear hair cell number
Expand Tier I Mouse GO 933 Genes GS178813: GO:0046983 protein dimerization activity
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Human GO 1136 Genes GS205691: GO:0022008 neurogenesis
Expand Tier I Mouse GO 8 Genes GS193044: GO:0050957 equilibrioception
Expand Tier I Mouse 735 Genes GS135274: "alcohol preference locus 18, male specific" (Alcp18, Published QTL Chr 11)
Expand Tier I Human 515 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human GO 969 Genes GS195570: GO:0046983 protein dimerization activity
Expand Tier I Mouse MP 55 Genes GS168880: MP:0004736 abnormal distortion product otoacoustic emission
Expand Tier I Mouse MP 164 Genes GS163724: MP:0000436 abnormal head movements
Expand Tier I Human GO 2545 Genes GS203335: GO:0048513 organ development
Expand Tier I Mouse GO 55 Genes GS188801: GO:0042490 mechanoreceptor differentiation
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Mouse MP 51 Genes GS163695: MP:0006090 abnormal utricle morphology
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 607 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human GO 493 Genes GS201848: GO:0048598 embryonic morphogenesis
Expand Tier I Human 89 Genes GS173329: HP:0000682 Abnormality of dental enamel
Expand Tier I Human GO 1588 Genes GS196772: GO:0048646 anatomical structure formation involved in morphogenesis
Expand Tier I Mouse GO 1850 Genes GS186562: GO:0009653 anatomical structure morphogenesis
Expand Tier I Mouse MP 23 Genes GS166929: MP:0004333 abnormal utricular macula morphology
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 MP 46 Genes GS166904: MP:0001485 abnormal pinna reflex
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 172 Genes GS173476: HP:0002311 Incoordination
Expand Tier I Human GO 8 Genes GS209985: GO:0050957 equilibrioception
Expand Tier I Mouse MP 68 Genes GS168762: MP:0005423 abnormal somatic nervous system physiology
Expand Tier I Mouse MP 2200 Genes GS165465: MP:0003633 abnormal nervous system physiology
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 Human 52 Genes GS174577: HP:0009924 Aplasia/Hypoplasia involving the nose
Expand Tier I Human GO 205 Genes GS209987: GO:0050953 sensory perception of light stimulus
Expand Tier I Mouse MP 21 Genes GS163528: MP:0004434 abnormal cochlear outer hair cell physiology
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 Mouse GO 133 Genes GS193043: GO:0050954 sensory perception of mechanical stimulus
Expand Tier I Human 34 Genes GS172732: HP:0001751 Vestibular dysfunction
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 1003 Genes GS136677: skull morphology 16 (Skull16, Published QTL Chr 11)
Expand Tier I Mouse GO 863 Genes GS177902: GO:0042802 identical protein binding
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Mouse 1038 Genes GS136434: pulmonary adenoma susceptibility 5b (Pas5b, Published QTL Chr 11)
Expand Tier I Human GO 1067 Genes GS196002: GO:0048699 generation of neurons
Expand Tier I Human GO 329 Genes GS198056: GO:0048568 embryonic organ development
Expand Tier I Mouse MP 17 Genes GS162966: MP:0004324 vestibular hair cell degeneration
Expand Tier I Human 1 Genes GS173492: HP:0004646 Hypoplasia of the nasal bone
Expand Tier I Mouse GO 2876 Genes GS182474: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Mouse 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 GO 37 Genes GS181873: GO:0043954 cellular component maintenance
Expand Tier I Mouse MP 710 Genes GS167922: MP:0000959 abnormal somatic sensory system morphology
Expand Tier I Human GO 2368 Genes GS207365: GO:0005829 cytosol
Expand Tier I Human GO 132 Genes GS209984: GO:0050954 sensory perception of mechanical stimulus
Expand Tier I Mouse MP 438 Genes GS165390: MP:0003224 neuron degeneration
Expand Tier I Mouse 710 Genes GS136328: non-insulin-dependent diabetes mellitus 4 (Nidd4, Published QTL Chr 11)
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 Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Mouse MP 14488 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Mouse GO 2538 Genes GS190893: GO:0030154 cell differentiation
Expand Tier I Human GO 4283 Genes GS197009: GO:0005886 plasma membrane
Expand Tier I Mouse GO 323 Genes GS188368: GO:0015629 actin cytoskeleton
Expand Tier I Human GO 792 Genes GS205616: GO:0009887 organ morphogenesis
Expand Tier I Mouse MP 68 Genes GS165873: MP:0004404 cochlear outer hair cell degeneration
Expand Tier I Human 1 Genes GS171749: HP:0010937 Abnormality of the nasal skeleton
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 45 Genes GS168065: MP:0002623 abnormal vestibular hair cell morphology
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 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 792 Genes GS136514: protein kinase C content in lungs (Pkccl, Published QTL Chr 11)
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 Mouse MP 11 Genes GS163829: MP:0011060 abnormal kinocilium morphology
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 Human GO 364 Genes GS205224: GO:0015629 actin cytoskeleton