Gene Details



USH1G and homologs in 6 species are found in 618 GeneSets:


- Entrez   - GeneNetwork   - 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 II Human 557 Genes GS235620: [MeSH] Sensation Disorders : D012678
Expand Tier II Human 2152 Genes GS234139: [MeSH] Biophysical Processes : D055597
Expand Tier I Mouse 1003 Genes GS136433: pulmonary adenoma susceptibility 5a (Pas5a, Published QTL Chr 11)
Expand Tier II Human 703 Genes GS237881: [MeSH] Retinal Diseases : D012164
Expand Tier II Human 19440 Genes GS241666: [MeSH] Sequence Homology, Amino Acid : D017386
Expand Tier III Rat 167 Genes GS224097: Collagen induced arthritis QTL 28 (Cia28 Published QTL Chr 10)
Expand Tier II Human 19667 Genes GS245646: [MeSH] Hydrolases : D006867
Expand Tier I Mouse MP 50 Genes GS167803: MP:0005307 head tossing
Expand Tier II Human 2932 Genes GS236094: [MeSH] Scleroproteins : D012596
Expand Tier I Mouse MP 1698 Genes GS164220: MP:0002882 abnormal neuron morphology
Expand Tier II Human 350 Genes GS236887: [MeSH] Ear Diseases : D004427
Expand Tier I Mouse MP 279 Genes GS163596: MP:0000026 abnormal inner ear morphology
Expand Tier II Human 187 Genes GS236163: [MeSH] Deafness : D003638
Expand Tier I Human GO 7609 Genes GS201949: GO:0044699 single-organism process
Expand Tier II Human 22403 Genes GS244084: [MeSH] Phenotype : D010641
Expand Tier I Mouse MP 18 Genes GS166834: MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology
Expand Tier III Rat 860 Genes GS223141: Bone structure and strength QTL 25 (Bss25 Published QTL Chr 10)
Expand Tier III Rat 895 Genes GS224914: Blood pressure QTL 300 (Bp300 Published QTL Chr 10)
Expand Tier I Mouse GO 3706 Genes GS188641: GO:0071944 cell periphery
Expand Tier I Human 657 Genes GS227315: MSigDB Geneset - TGACATY_UNKNOWN
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 II Human 700 Genes GS235429: [MeSH] Ear : D004423
Expand Tier II Human 8606 Genes GS243926: [MeSH] Exons : D005091
Expand Tier I Mouse MP 5 Genes GS168036: MP:0004466 short cochlear outer hair cells
Expand Tier II Human 12421 Genes GS239540: [MeSH] Heterochromatin : D006570
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Human 2254 Genes GS230495: MSigDB Geneset - GGGAGGRR_V$MAZ_Q6
Expand Tier III Rat 375 Genes GS224238: Blood pressure QTL 280 (Bp280 Published QTL Chr 10)
Expand Tier III Rat 1845 Genes GS224997: Collagen induced arthritis QTL 21 (Cia21 Published QTL Chr 10)
Expand Tier I Human 152 Genes GS174979: HP:0011061 Abnormality of dental structure
Expand Tier I Human 241 Genes GS231685: PC Geneset - "V$LFA1_Q6" pathway genes
Expand Tier I Mouse MP 413 Genes GS165253: MP:0001399 hyperactivity
Expand Tier II Human 11812 Genes GS236947: [MeSH] Brain : D001921
Expand Tier I Mouse GO 454 Genes GS181012: GO:0007423 sensory organ development
Expand Tier II Human 70216 Genes GS235234: [MeSH] Biochemical Phenomena : D001669
Expand Tier III Rat 370 Genes GS223376: Body weight QTL 57 (Bw57 Published QTL Chr 10)
Expand Tier I Mouse GO 23778 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 II Human 4661 Genes GS238716: [MeSH] Genetic Linkage : D008040
Expand Tier I Mouse GO 123 Genes GS193046: GO:0050953 sensory perception of light stimulus
Expand Tier I Human GO 565 Genes GS194646: GO:0042803 protein homodimerization activity
Expand Tier II Human 12580 Genes GS238462: [MeSH] Interspersed Repetitive Sequences : D020071
Expand Tier II Human 15702 Genes GS245264: [MeSH] Nervous System : D009420
Expand Tier II Human 465 Genes GS235765: [MeSH] Chromosomes, Human, Pair 17 : D002886
Expand Tier I Human 375 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier II Human 10433 Genes GS239764: [MeSH] Glycoproteins : D006023
Expand Tier I Human GO 2653 Genes GS207797: GO:0030154 cell differentiation
Expand Tier II Human 70252 Genes GS238030: [MeSH] Chemical Phenomena : D055598
Expand Tier II Human 745 Genes GS238514: [MeSH] Otorhinolaryngologic Diseases : D010038
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 4061 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier III Rat 914 Genes GS223396: Experimental allergic encephalomyelitis QTL 18 (Eae18 Published QTL Chr 10)
Expand Tier II Human 1773 Genes GS235887: [MeSH] Behavior, Animal : D001522
Expand Tier II Human 466 Genes GS235770: [MeSH] Chromosomes, Human, Pair 10 : D002879
Expand Tier I Human 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 4014 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier III Rat 860 Genes GS223270: Bone structure and strength QTL 33 (Bss33 Published QTL Chr 10)
Expand Tier II Human 7591 Genes GS239955: [MeSH] Amino Acid Motifs : D020816
Expand Tier I Human 636 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier II Human 3455 Genes GS239907: [MeSH] Cell Surface Extensions : D022081
Expand Tier II Human 30225 Genes GS236481: [MeSH] Enzymes : D004798
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 III Rat 860 Genes GS223539: Bone mineral density QTL 57 (Bmd57 Published QTL Chr 10)
Expand Tier I Mouse MP 228 Genes GS163320: MP:0000031 abnormal cochlea morphology
Expand Tier II Human 2536 Genes GS240585: [MeSH] Sensory Receptor Cells : D011984
Expand Tier I Mouse GO 187 Genes GS187229: GO:0043583 ear development
Expand Tier I Mouse MP 2893 Genes GS165466: MP:0003632 abnormal nervous system morphology
Expand Tier II Human 5149 Genes GS237067: [MeSH] Contractile Proteins : D003285
Expand Tier I Mouse 1046 Genes GS135496: brain weight QTL 1 (Brwq1, Published QTL Chr 11)
Expand Tier III Rat 532 Genes GS223666: Body weight QTL 102 (Bw102 Published QTL Chr 10)
Expand Tier I Mouse MP 53 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 187 Genes GS169758: MP:0004765 decreased brainstem auditory evoked potential
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier II Human 1807 Genes GS236935: [MeSH] Rhombencephalon : D012249
Expand Tier I Human 136 Genes GS175674: HP:0007360 Aplasia/Hypoplasia of the cerebellum
Expand Tier II Human 29 Genes GS243235: [MeSH] Labyrinth Diseases : D007759
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
Expand Tier II Human 2660 Genes GS244236: [MeSH] Homozygote : D006720
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 1786 Genes GS208893: GO:0005856 cytoskeleton
Expand Tier I Human GO 12162 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 III Rat 775 Genes GS224977: Collagen induced arthritis QTL 27 (Cia27 Published QTL Chr 10)
Expand Tier I Human 590 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 187 Genes GS168193: MP:0000966 decreased sensory neuron number
Expand Tier I Mouse GO 3597 Genes GS188142: GO:0048856 anatomical structure development
Expand Tier II Human 8197 Genes GS239290: [MeSH] Cell Line, Transformed : D002461
Expand Tier I Mouse MP 171 Genes GS168066: MP:0002622 abnormal cochlear hair cell morphology
Expand Tier I Mouse MP 89 Genes GS169795: MP:0004427 abnormal vestibular labyrinth morphology
Expand Tier I Human 253 Genes GS232238: PC Geneset - "V$PAX_Q6" pathway genes
Expand Tier I Mouse MP 58 Genes GS168293: MP:0004742 abnormal vestibular system physiology
Expand Tier I Human 244 Genes GS227684: MSigDB Geneset - V$LMO2COM_02
Expand Tier I Human 764 Genes GS228358: MSigDB Geneset - RNGTGGGC_UNKNOWN
Expand Tier I Human 233 Genes GS231825: PC Geneset - "V$GATA3_01" pathway genes
Expand Tier II Human 50 Genes GS234806: [MeSH] Saccule and Utricle : D012444
Expand Tier I Mouse GO 348 Genes GS181267: GO:0048568 embryonic organ development
Expand Tier II Human 9858 Genes GS242870: [MeSH] Polymorphism, Genetic : D011110
Expand Tier I Human 289 Genes GS228198: MSigDB Geneset - TGATTTRY_V$GFI1_01
Expand Tier II Human 37746 Genes GS240208: [MeSH] Amino Acid Sequence : D000595
Expand Tier II Human 21236 Genes GS240239: [MeSH] Sequence Homology : D017385
Expand Tier III Rat 974 Genes GS224407: Insulin level QTL 15 (Insul15 Published QTL Chr 10)
Expand Tier I Mouse 801 Genes GS136780: seizure susceptibility 3 (Szs3, Published QTL Chr 11)
Expand Tier I Mouse MP 799 Genes GS163226: MP:0003312 abnormal locomotor coordination
Expand Tier I Human GO 4338 Genes GS205500: GO:0071944 cell periphery
Expand Tier III Rat 298 Genes GS224702: Brain ventricular dilatation QTL 2 (Bvd2 Published QTL Chr 10)
Expand Tier I Human 342 Genes GS174378: HP:0000518 Cataract
Expand Tier II Human 19 Genes GS234393: [MeSH] Vestibular Diseases : D015837
Expand Tier III Rat 178 Genes GS224584: Oil induced arthritis QTL 6 (Oia6 Published QTL Chr 10)
Expand Tier I Human GO 38 Genes GS198664: GO:0043954 cellular component maintenance
Expand Tier II Human 352 Genes GS238427: [MeSH] Neuroepithelial Cells : D046569
Expand Tier I Human GO 493 Genes GS209225: GO:0007600 sensory perception
Expand Tier II Human 35836 Genes GS242639: [MeSH] Metabolic Phenomena : D055754
Expand Tier II Human 9151 Genes GS238044: [MeSH] Acid Anhydride Hydrolases : D017766
Expand Tier II Human 497 Genes GS244503: [MeSH] Mechanoreceptors : D008465
Expand Tier II Human 18727 Genes GS236759: [MeSH] Intranuclear Space : D042581
Expand Tier I Human 607 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Mouse GO 500 Genes GS185033: GO:0048598 embryonic morphogenesis
Expand Tier II Human 12291 Genes GS238872: [MeSH] Central Nervous System : D002490
Expand Tier I Human 49 Genes GS173812: HP:0000738 Hallucinations
Expand Tier I Human GO 435 Genes GS197802: GO:0007423 sensory organ development
Expand Tier I Human 413 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier II Human 6887 Genes GS234190: [MeSH] Polymers : D011108
Expand Tier I Mouse GO 912 Genes GS179236: GO:0048699 generation of neurons
Expand Tier II Human 7085 Genes GS244254: [MeSH] Antigens, Surface : D000954
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 II Human 14860 Genes GS240463: [MeSH] Chromatin : D002843
Expand Tier II Human 61866 Genes GS235287: [MeSH] Proteins : D011506
Expand Tier I Human GO 898 Genes GS201125: GO:0009790 embryo development
Expand Tier III Rat 1499 Genes GS224988: Collagen induced arthritis QTL 23 (Cia23 Published QTL Chr 10)
Expand Tier II Human 46864 Genes GS243659: [MeSH] RNA, Messenger : D012333
Expand Tier II Human 4510 Genes GS241347: [MeSH] Microfilament Proteins : D008840
Expand Tier I Mouse MP 178 Genes GS163068: MP:0000045 abnormal hair cell morphology
Expand Tier III Rat 167 Genes GS223474: Pristane induced arthritis QTL 25 (Pia25 Published QTL Chr 10)
Expand Tier II Human 15116 Genes GS243569: [MeSH] Macromolecular Substances : D046911
Expand Tier II Human 56846 Genes GS235305: [MeSH] DNA, Complementary : D018076
Expand Tier I Mouse MP 13 Genes GS164027: MP:0004814 reduced linear vestibular evoked potential
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier II Human 6533 Genes GS244610: [MeSH] Nervous System Diseases : D009422
Expand Tier I Mouse 1060 Genes GS135973: wound healing/regeneration 10 (Heal10, Published QTL Chr 11)
Expand Tier II Human 1998 Genes GS244732: [MeSH] Protein Precursors : D011498
Expand Tier III Rat 2054 Genes GS224162: Mammary tumor resistance QTL 7 (Mamtr7 Published QTL Chr 10)
Expand Tier I Human 532 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 MP 255 Genes GS164126: MP:0001388 abnormal stationary movement
Expand Tier II Human 39830 Genes GS245976: [MeSH] Cellular Structures : D022082
Expand Tier III Rat 1941 Genes GS224152: Glucose level QTL 60 (Gluco60 Published QTL Chr 10)
Expand Tier I Human 124 Genes GS175492: HP:0000512 Abnormal electroretinogram
Expand Tier II Human 26 Genes GS237994: [MeSH] Deaf-Blind Disorders : D054062
Expand Tier I Mouse 715 Genes GS135815: ethanol induced ataxia 10 (Etax10, Published QTL Chr 11)
Expand Tier II Human 67553 Genes GS240572: [MeSH] DNA : D004247
Expand Tier II Human 31495 Genes GS241930: [MeSH] Mutation : D009154
Expand Tier I Mouse MP 30 Genes GS165256: MP:0001395 bidirectional circling
Expand Tier II Human 5111 Genes GS242217: [MeSH] Muscle Proteins : D009124
Expand Tier I Mouse MP 175 Genes GS164059: MP:0006325 impaired hearing
Expand Tier I Mouse MP 29 Genes GS168879: MP:0004737 absent distortion product otoacoustic emissions
Expand Tier I Human GO 3116 Genes GS197892: GO:0043228 non-membrane-bounded organelle
Expand Tier I Human 281 Genes GS231748: PC Geneset - "TGATTTRY_V$GFI1_01" pathway genes
Expand Tier II Human 2632 Genes GS242312: [MeSH] Extracellular Matrix Proteins : D016326
Expand Tier II Human 43280 Genes GS236911: [MeSH] Transcription, Genetic : D014158
Expand Tier III Rat 1495 Genes GS223555: Stress response QTL 5 (Stresp5 Published QTL Chr 10)
Expand Tier II Human 65203 Genes GS235942: [MeSH] Genetic Processes : D039361
Expand Tier I Mouse GO 903 Genes GS184317: GO:0009790 embryo development
Expand Tier II Human 253 Genes GS236399: [MeSH] Consanguinity : D003241
Expand Tier I Human GO 5623 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 III Rat 373 Genes GS223102: Blood pressure QTL 149 (Bp149 Published QTL Chr 10)
Expand Tier II Human 640 Genes GS237443: [MeSH] Ear, Inner : D007758
Expand Tier III Rat 448 Genes GS224581: Oil induced arthritis QTL 3 (Oia3 Published QTL Chr 10)
Expand Tier I Mouse MP 3159 Genes GS169828: MP:0005386 behavior/neurological phenotype
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier I Mouse 1046 Genes GS136952: weight gain in high growth mice 7 (Wg7, Published QTL Chr 11)
Expand Tier II Human 61 Genes GS238726: [MeSH] Blindness : D001766
Expand Tier II Human 79329 Genes GS243722: [MeSH] Genetic Structures : D040342
Expand Tier II Human 67130 Genes GS241889: [MeSH] Molecular Structure : D015394
Expand Tier I Mouse 1046 Genes GS135812: estradiol regulated response QTL 3 (Estq3, Published QTL Chr 11)
Expand Tier III Rat 878 Genes GS224321: Blood pressure QTL 9 (Bp9 Published QTL Chr 10)
Expand Tier I Mouse MP 959 Genes GS166244: MP:0002752 abnormal somatic nervous system morphology
Expand Tier II Human 8187 Genes GS234648: [MeSH] Alleles : D000483
Expand Tier I Human GO 9088 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human GO 2047 Genes GS203406: GO:0009653 anatomical structure morphogenesis
Expand Tier I Human 177 Genes GS227945: MSigDB Geneset - chr17q25
Expand Tier II Human 59585 Genes GS234621: [MeSH] Chemical Actions and Uses : D020164
Expand Tier II Human 62071 Genes GS235061: [MeSH] Amino Acids, Peptides, and Proteins : D000602
Expand Tier I Human 198 Genes GS230311: MSigDB Geneset - V$GATA_Q6
Expand Tier I Human 401 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Mouse 767 Genes GS135792: epilepsy 6 (El6, Published QTL Chr 11)
Expand Tier II Human 9312 Genes GS236231: [MeSH] Antigens : D000941
Expand Tier II Mouse 780 Genes GS84255: alcohol preference locus (Published QTL, Chr 11)
Expand Tier II Human 23706 Genes GS235056: [MeSH] Peptides : D010455
Expand Tier II Human 47536 Genes GS236298: [MeSH] Gene Expression : D015870
Expand Tier II Human 3773 Genes GS234965: [MeSH] Cell Adhesion Molecules : D015815
Expand Tier II Human 18907 Genes GS242148: [MeSH] Cell Nucleus Structures : D022003
Expand Tier II Human 13815 Genes GS240409: [MeSH] Drosophila Proteins : D029721
Expand Tier I Human 202 Genes GS174764: HP:0007367 Atrophy/Degeneration affecting the central nervous system
Expand Tier II Human 3287 Genes GS237404: [MeSH] Chromosomes, Human, 6-12 and X : D002906
Expand Tier I Human GO 4085 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Mouse MP 3522 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 Mouse MP 32 Genes GS164571: MP:0004432 abnormal cochlear hair cell physiology
Expand Tier I Human 356 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Human 164 Genes GS174994: HP:0002059 Cerebral atrophy
Expand Tier II Human 36279 Genes GS241850: [MeSH] Genetic Variation : D014644
Expand Tier I Mouse MP 262 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 III Rat 263 Genes GS224185: Bone mineral density QTL 16 (Bmd16 Published QTL Chr 10)
Expand Tier II Human 38809 Genes GS236076: [MeSH] Protein Conformation : D011487
Expand Tier II Human 3004 Genes GS240265: [MeSH] Neurons, Afferent : D009475
Expand Tier II Human 21260 Genes GS238232: [MeSH] Nucleoproteins : D009698
Expand Tier I Human 361 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human 115 Genes GS230191: MSigDB Geneset - V$MEIS1AHOXA9_01
Expand Tier I Mouse MP 2283 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 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Mouse MP 864 Genes GS169390: MP:0002067 abnormal sensory capabilities/reflexes/nociception
Expand Tier I Human 695 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human 541 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Mouse GO 10879 Genes GS181473: GO:0005488 binding
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 510 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 Human GO 7717 Genes GS207616: GO:0016020 membrane
Expand Tier II Human 8754 Genes GS241960: [MeSH] Protein Structure, Secondary : D017433
Expand Tier I Mouse GO 3614 Genes GS180229: GO:0005886 plasma membrane
Expand Tier I Human GO 1722 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 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 II Human 50108 Genes GS239769: [MeSH] Gene Library : D015723
Expand Tier I Mouse 1281 Genes GS129115: collagen induced arthritis 40 (Cia40 Published QTL Chr 11)
Expand Tier II Human 58105 Genes GS242107: [MeSH] Chemical Processes : D055599
Expand Tier II Human 32929 Genes GS243578: [MeSH] Reading Frames : D016364
Expand Tier I Mouse 981 Genes GS136789: tail length QTL 8 (Tailq8, Published QTL Chr 11)
Expand Tier II Human 29996 Genes GS237597: [MeSH] Cell Physiological Processes : D055648
Expand Tier I Human GO 3506 Genes GS193991: GO:0048731 system development
Expand Tier I Mouse MP 10 Genes GS163543: MP:0004431 abnormal hair cell mechanoelectric transduction
Expand Tier III Rat 1859 Genes GS224636: Cardiac mass QTL 31 (Cm31 Published QTL Chr 10)
Expand Tier I Mouse MP 628 Genes GS164023: MP:0001961 abnormal reflex
Expand Tier I Mouse 792 Genes GS136831: TNF-induced lethal shock susceptibility 2 (Tilss2, Published QTL Chr 11)
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 487 Genes GS166123: MP:0002102 abnormal ear morphology
Expand Tier II Human 5853 Genes GS241597: [MeSH] Disease Models, Animal : D004195
Expand Tier I Mouse MP 51 Genes GS169760: MP:0004763 absent brainstem auditory evoked potential
Expand Tier II Human 23569 Genes GS235276: [MeSH] Signal Transduction : D015398
Expand Tier III Rat 974 Genes GS223703: Serum leptin concentration QTL 8 (Slep8 Published QTL Chr 10)
Expand Tier I Mouse GO 2138 Genes GS186067: GO:0050877 neurological system process
Expand Tier II Human 8645 Genes GS234354: [MeSH] Cytoskeletal Proteins : D003598
Expand Tier I Mouse MP 14 Genes GS165668: MP:0004524 short cochlear hair cell stereocilia
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier II Human 3244 Genes GS240069: [MeSH] Microtubule Proteins : D008868
Expand Tier I Mouse MP 23 Genes GS167591: MP:0004330 abnormal vestibular saccular macula morphology
Expand Tier II Human 839 Genes GS238687: [MeSH] Disease : D004194
Expand Tier I Mouse GO 2498 Genes GS193018: GO:0003008 system process
Expand Tier II Human 821 Genes GS235519: [MeSH] Syndrome : D013577
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 II Human 73736 Genes GS238575: [MeSH] Nucleic Acids : D009696
Expand Tier II Human 3871 Genes GS237854: [MeSH] Peripheral Nervous System : D017933
Expand Tier II Human 11815 Genes GS238961: [MeSH] Nerve Tissue Proteins : D009419
Expand Tier I Human GO 1135 Genes GS205691: GO:0022008 neurogenesis
Expand Tier II Human 1240 Genes GS238245: [MeSH] Cerebellum : D002531
Expand Tier I Mouse GO 8 Genes GS193044: GO:0050957 equilibrioception
Expand Tier II Human 22498 Genes GS245206: [MeSH] Cell Nucleus : D002467
Expand Tier I Mouse 735 Genes GS135274: "alcohol preference locus 18, male specific" (Alcp18, Published QTL Chr 11)
Expand Tier I Human 513 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human GO 966 Genes GS195570: GO:0046983 protein dimerization activity
Expand Tier I Mouse MP 51 Genes GS168880: MP:0004736 abnormal distortion product otoacoustic emission
Expand Tier III Rat 1341 Genes GS224784: Carrageenan-induced inflammation QTL 1 (Cari1 Published QTL Chr 10)
Expand Tier I Mouse MP 159 Genes GS163724: MP:0000436 abnormal head movements
Expand Tier I Human GO 2539 Genes GS203335: GO:0048513 organ development
Expand Tier II Human 58261 Genes GS239502: [MeSH] Nucleic Acid Probes : D015341
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 23849 Genes GS180164: GO:0008150 biological_process
Expand Tier II Human 30111 Genes GS244835: [MeSH] Chromosomes : D002875
Expand Tier III Rat 1737 Genes GS223978: Pristane induced arthritis QTL 10 (Pia10 Published QTL Chr 10)
Expand Tier II Human 3385 Genes GS237069: [MeSH] Congenital Abnormalities : D000013
Expand Tier I Mouse MP 50 Genes GS163695: MP:0006090 abnormal utricle morphology
Expand Tier I Human 917 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 604 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human GO 492 Genes GS201848: GO:0048598 embryonic morphogenesis
Expand Tier I Human 88 Genes GS173329: HP:0000682 Abnormality of dental enamel
Expand Tier II Human 52165 Genes GS242059: [MeSH] Cells : D002477
Expand Tier III Rat 401 Genes GS223064: Mammary carcinoma susceptibility QTL 15 (Mcs15 Published QTL Chr 10)
Expand Tier II Human 2272 Genes GS239652: [MeSH] Genes, Recessive : D005808
Expand Tier II Human 161 Genes GS238585: [MeSH] Retinitis Pigmentosa : D012174
Expand Tier II Human 2438 Genes GS238953: [MeSH] Neurologic Manifestations : D009461
Expand Tier I Human GO 1587 Genes GS196772: GO:0048646 anatomical structure formation involved in morphogenesis
Expand Tier III Rat 974 Genes GS224708: Serum cholesterol level QTL 65 (Scl65 Published QTL Chr 10)
Expand Tier II Human 73996 Genes GS244482: [MeSH] Nucleic Acids, Nucleotides, and Nucleosides : D009706
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 14537 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 45 Genes GS166904: MP:0001485 abnormal pinna reflex
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 170 Genes GS173476: HP:0002311 Incoordination
Expand Tier II Human 18456 Genes GS243735: [MeSH] Biological Factors : D001685
Expand Tier I Human GO 8 Genes GS209985: GO:0050957 equilibrioception
Expand Tier II Human 58105 Genes GS235797: [MeSH] DNA Probes : D015342
Expand Tier I Mouse MP 66 Genes GS168762: MP:0005423 abnormal somatic nervous system physiology
Expand Tier III Rat 1737 Genes GS224614: Adjuvant induced arthritis QTL 5 (Aia5 Published QTL Chr 10)
Expand Tier II Human 8647 Genes GS242147: [MeSH] Fibroblasts : D005347
Expand Tier III Rat 811 Genes GS223260: Neuroinflammation QTL 7 (Neuinf7 Published QTL Chr 10)
Expand Tier I Mouse MP 2111 Genes GS165465: MP:0003633 abnormal nervous system physiology
Expand Tier I Human 386 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Mouse GO 226 Genes GS181262: GO:0048562 embryonic organ morphogenesis
Expand Tier II Human 30298 Genes GS242332: [MeSH] Cell Physiological Phenomena : D002468
Expand Tier II Human 58023 Genes GS235242: [MeSH] Biochemical Processes : D055438
Expand Tier II Human 109 Genes GS237886: [MeSH] Vision Disorders : D014786
Expand Tier III Rat 931 Genes GS224933: Adjuvant induced arthritis QTL 19 (Aia19 Published QTL Chr 10)
Expand Tier II Human 52588 Genes GS245685: [MeSH] RNA : D012313
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 II Human 5596 Genes GS235557: [MeSH] Animal Diseases : D000820
Expand Tier II Human 12397 Genes GS235736: [MeSH] DNA Transposable Elements : D004251
Expand Tier I Mouse MP 21 Genes GS163528: MP:0004434 abnormal cochlear outer hair cell physiology
Expand Tier I Human 2227 Genes GS232290: PC Geneset - "GGGAGGRR_V$MAZ_Q6" pathway genes
Expand Tier I Human GO 75 Genes GS204969: GO:0050905 neuromuscular process
Expand Tier I Mouse MP 55 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 240 Genes GS227927: MSigDB Geneset - V$GATA3_01
Expand Tier I Human 34 Genes GS172732: HP:0001751 Vestibular dysfunction
Expand Tier I Human 273 Genes GS229238: MSigDB Geneset - YKACATTT_UNKNOWN
Expand Tier III Rat 234 Genes GS223760: Collagen induced arthritis QTL 5 (Cia5 Published QTL Chr 10)
Expand Tier I Human 42 Genes GS174449: HP:0001123 Visual field defect
Expand Tier II Human 28877 Genes GS238592: [MeSH] Cells, Cultured : D002478
Expand Tier I Human 136 Genes GS232407: PC Geneset - "V$MEIS1BHOXA9_01" pathway genes
Expand Tier I Human 411 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier III Rat 618 Genes GS223217: Glomerulus QTL 25 (Glom25 Published QTL Chr 10)
Expand Tier II Human 11221 Genes GS237257: [MeSH] Pathologic Processes : D010335
Expand Tier I Human 141 Genes GS230584: MSigDB Geneset - V$MEIS1BHOXA9_01
Expand Tier I Mouse 1003 Genes GS136677: skull morphology 16 (Skull16, Published QTL Chr 11)
Expand Tier I Mouse GO 863 Genes GS177902: GO:0042802 identical protein binding
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Mouse 1038 Genes GS136434: pulmonary adenoma susceptibility 5b (Pas5b, Published QTL Chr 11)
Expand Tier II Human 3012 Genes GS234181: [MeSH] Retina : D012160
Expand Tier I Human GO 1066 Genes GS196002: GO:0048699 generation of neurons
Expand Tier I Human 488 Genes GS232087: PC Geneset - "TCANNTGAY_V$SREBP1_01" pathway genes
Expand Tier I Human GO 329 Genes GS198056: GO:0048568 embryonic organ development
Expand Tier III Rat 113 Genes GS223390: Experimental allergic encephalomyelitis QTL 12 (Eae12 Published QTL Chr 10)
Expand Tier I Mouse MP 17 Genes GS162966: MP:0004324 vestibular hair cell degeneration
Expand Tier II Human 23211 Genes GS235538: [MeSH] Protein Binding : D011485
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 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier II Human 10133 Genes GS235960: [MeSH] Connective Tissue Cells : D003239
Expand Tier II Human 5399 Genes GS243780: [MeSH] COS Cells : D019556
Expand Tier I Mouse MP 142 Genes GS169847: MP:0004399 abnormal cochlear outer hair cell morphology
Expand Tier II Human 10298 Genes GS238960: [MeSH] Membrane Glycoproteins : D008562
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 II Human 15731 Genes GS236183: [MeSH] Chromosome Structures : D022004
Expand Tier I Mouse MP 702 Genes GS167922: MP:0000959 abnormal somatic sensory system morphology
Expand Tier II Human 2555 Genes GS242366: [MeSH] Inheritance Patterns : D040582
Expand Tier I Human GO 2364 Genes GS207365: GO:0005829 cytosol
Expand Tier II Human 896 Genes GS236992: [MeSH] Chromosomes, Human, 16-18 : D002902
Expand Tier I Human GO 132 Genes GS209984: GO:0050954 sensory perception of mechanical stimulus
Expand Tier II Human 9707 Genes GS235744: [MeSH] Neurons : D009474
Expand Tier I Mouse MP 433 Genes GS165390: MP:0003224 neuron degeneration
Expand Tier II Human 4906 Genes GS239789: [MeSH] Adenosine Triphosphatases : D000251
Expand Tier III Rat 1387 Genes GS224316: Blood pressure QTL 1 (Bp1 Published QTL Chr 10)
Expand Tier I Human 200 Genes GS232060: PC Geneset - "V$GATA_Q6" pathway genes
Expand Tier I Mouse 710 Genes GS136328: non-insulin-dependent diabetes mellitus 4 (Nidd4, Published QTL Chr 11)
Expand Tier II Human 58766 Genes GS243866: [MeSH] Laboratory Chemicals : D019995
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier II Human 12283 Genes GS244576: [MeSH] Genome, Insect : D049750
Expand Tier III Rat 967 Genes GS224952: CIA Autoantibody QTL 2 (Ciaa2 Published QTL Chr 10)
Expand Tier I Human 757 Genes GS228632: MSigDB Geneset - CTGCAGY_UNKNOWN
Expand Tier I Human 93 Genes GS176289: HP:0002120 Cerebral cortical atrophy
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Mouse MP 11449 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier II Human 23476 Genes GS237836: [MeSH] Carrier Proteins : D002352
Expand Tier I Mouse GO 2538 Genes GS190893: GO:0030154 cell differentiation
Expand Tier II Human 2037 Genes GS237303: [MeSH] Mutation, Missense : D020125
Expand Tier II Human 16221 Genes GS239275: [MeSH] Intracellular Signaling Peptides and Proteins : D047908
Expand Tier II Human 58901 Genes GS243233: [MeSH] Specialty Uses of Chemicals : D020313
Expand Tier I Human GO 4250 Genes GS197009: GO:0005886 plasma membrane
Expand Tier II Human 289 Genes GS243183: [MeSH] Hearing Loss : D034381
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 III Rat 856 Genes GS223659: Body weight QTL 106 (Bw106 Published QTL Chr 10)
Expand Tier II Human 2584 Genes GS235299: [MeSH] Physical Processes : D055586
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 7308 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 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier II Human 482 Genes GS235047: [MeSH] Retinal Degeneration : D012162
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 413 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier II Human 36882 Genes GS236241: [MeSH] Protein Structure, Tertiary : D017434
Expand Tier I Mouse 792 Genes GS136514: protein kinase C content in lungs (Pkccl, Published QTL Chr 11)
Expand Tier I Human GO 2816 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 II Human 3301 Genes GS241289: [MeSH] Behavior : D001519
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 II Human 3786 Genes GS241536: [MeSH] Immunity : D007109
Expand Tier I Human GO 363 Genes GS205224: GO:0015629 actin cytoskeleton
Expand Tier I Mouse MP 16 Genes GS165666: MP:0004523 decreased cochlear hair cell stereocilia number
Expand Tier II Human 14570 Genes GS237160: [MeSH] Repetitive Sequences, Nucleic Acid : D012091
Expand Tier I Human GO 95 Genes GS197513: GO:0042472 inner ear morphogenesis
Expand Tier I Mouse MP 94 Genes GS165787: MP:0001522 impaired swimming
Expand Tier II Human 1294 Genes GS234220: [MeSH] Metencephalon : D020540
Expand Tier I Human 238 Genes GS232281: PC Geneset - "V$LMO2COM_02" pathway genes
Expand Tier III Rat 965 Genes GS224829: Bone structure and strength QTL 43 (Bss43 Published QTL Chr 10)
Expand Tier I Human 95 Genes GS176616: HP:0000662 Night blindness
Expand Tier II Human 2564 Genes GS240980: [MeSH] Immunity, Innate : D007113
Expand Tier I Human 187 Genes GS174247: HP:0000539 Abnormality of refraction
Expand Tier I Mouse MP 85 Genes GS167643: MP:0000034 abnormal vestibule morphology
Expand Tier II Human 7486 Genes GS240624: [MeSH] Adaptor Proteins, Signal Transducing : D048868
Expand Tier II Human 7137 Genes GS234179: [MeSH] DNA, Intergenic : D021901
Expand Tier I Human 245 Genes GS229555: MSigDB Geneset - V$LFA1_Q6
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Mouse MP 106 Genes GS168215: MP:0001967 deafness
Expand Tier I Human GO 985 Genes GS204095: GO:0030182 neuron differentiation
Expand Tier I Mouse GO 980 Genes GS188826: GO:0022008 neurogenesis
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier II Human 357 Genes GS237228: [MeSH] Eye Diseases, Hereditary : D015785
Expand Tier II Human 2118 Genes GS236633: [MeSH] Brain Stem : D001933
Expand Tier I Human GO 3116 Genes GS199272: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier I Mouse MP 33 Genes GS167452: MP:0004532 abnormal inner hair cell stereociliary bundle morphology
Expand Tier II Human 5871 Genes GS237484: [MeSH] Congenital, Hereditary, and Neonatal Diseases and Abnormalities : D009358
Expand Tier II Human 73356 Genes GS238415: [MeSH] Genome Components : D040481
Expand Tier I Human 837 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier II Human 1689 Genes GS240795: [MeSH] Eye Diseases : D005128
Expand Tier I Human 115 Genes GS228993: MSigDB Geneset - CCANNAGRKGGC_UNKNOWN
Expand Tier II Human 1323 Genes GS243817: [MeSH] Abnormalities, Multiple : D000015
Expand Tier II Human 3071 Genes GS237070: [MeSH] Biophysical Phenomena : D055592
Expand Tier I Mouse GO 1550 Genes GS192290: GO:0007600 sensory perception
Expand Tier I Mouse MP 7 Genes GS167450: MP:0004534 decreased inner hair cell stereocilia number
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Mouse MP 1589 Genes GS165260: MP:0001392 abnormal locomotor behavior
Expand Tier II Human 4970 Genes GS237241: [MeSH] Immune System Phenomena : D055633
Expand Tier II Human 39556 Genes GS238930: [MeSH] Molecular Conformation : D008968
Expand Tier I Mouse GO 6204 Genes GS184629: GO:0005515 protein binding
Expand Tier II Human 58262 Genes GS240750: [MeSH] Molecular Probes : D015335
Expand Tier III Rat 1737 Genes GS223091: Collagen induced arthritis QTL 20 (Cia20 Published QTL Chr 10)
Expand Tier I Mouse MP 179 Genes GS163498: MP:0003308 abnormal cochlear sensory epithelium morphology
Expand Tier I Mouse MP 11 Genes GS165679: MP:0004529 decreased outer hair cell stereocilia number
Expand Tier I Mouse MP 114 Genes GS169841: MP:0004393 abnormal cochlear inner hair cell morphology
Expand Tier III Rat 775 Genes GS224389: Pancreatic morphology QTL 2 (Pancm2 Published QTL Chr 10)
Expand Tier I Mouse MP 542 Genes GS165385: MP:0008946 abnormal neuron number
Expand Tier II Human 4244 Genes GS234130: [MeSH] Genetic Diseases, Inborn : D030342
Expand Tier I Human GO 856 Genes GS194645: GO:0042802 identical protein binding
Expand Tier I Human 470 Genes GS229382: MSigDB Geneset - TCANNTGAY_V$SREBP1_01
Expand Tier II Human 3824 Genes GS236425: [MeSH] Signs and Symptoms : D012816
Expand Tier III Rat 931 Genes GS224617: Adjuvant induced arthritis QTL 6 (Aia6 Published QTL Chr 10)
Expand Tier I Mouse MP 282 Genes GS169967: MP:0001408 stereotypic behavior
Expand Tier I Mouse 697 Genes GS135386: berghei resistance locus 2 (Berr2, Published QTL Chr 11)
Expand Tier II Human 55514 Genes GS238409: [MeSH] Gene Components : D040461
Expand Tier I Mouse MP 635 Genes GS164032: MP:0004811 abnormal neuron physiology
Expand Tier I Mouse MP 656 Genes GS165538: MP:0005377 hearing/vestibular/ear phenotype
Expand Tier I Mouse MP 569 Genes GS166743: MP:0002229 neurodegeneration
Expand Tier I Mouse GO 2279 Genes