Gene Details



USH1G and homologs in 7 species are found in 608 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 7747 Genes GS185131: GO:0044699 single-organism process
Expand Tier II Human 379 Genes GS235620: [MeSH] Sensation Disorders : D012678
Expand Tier II Human 1228 Genes GS234139: [MeSH] Biophysical Processes : D055597
Expand Tier I Mouse GO 1515 Genes GS338005: GO:0048468 cell development
Expand Tier II Mouse 1003 Genes GS136433: pulmonary adenoma susceptibility 5a (Pas5a, Published QTL Chr 11)
Expand Tier II Human 9028 Genes GS241666: [MeSH] Sequence Homology, Amino Acid : D017386
Expand Tier II Human 455 Genes GS237881: [MeSH] Retinal Diseases : D012164
Expand Tier II Human 8283 Genes GS245646: [MeSH] Hydrolases : D006867
Expand Tier II Rat 167 Genes GS224097: Collagen induced arthritis QTL 28 (Cia28 Published QTL Chr 10)
Expand Tier I Mouse MP 54 Genes GS167803: MP:0005307 head tossing
Expand Tier II Human 1638 Genes GS236094: [MeSH] Scleroproteins : D012596
Expand Tier I Mouse GO 1631 Genes GS334917: GO:0044446 intracellular organelle part
Expand Tier I Mouse MP 1190 Genes GS164220: MP:0002882 abnormal neuron morphology
Expand Tier II Human 251 Genes GS236887: [MeSH] Ear Diseases : D004427
Expand Tier I Mouse MP 260 Genes GS163596: MP:0000026 abnormal inner ear morphology
Expand Tier I Mouse GO 613 Genes GS338087: GO:0031175 neuron projection development
Expand Tier II Human 125 Genes GS236163: [MeSH] Deafness : D003638
Expand Tier I Human GO 49 Genes GS313315: GO:0001894 tissue homeostasis
Expand Tier I Human GO 7611 Genes GS201949: GO:0044699 single-organism process
Expand Tier II Human 9751 Genes GS244084: [MeSH] Phenotype : D010641
Expand Tier I Mouse MP 15 Genes GS166834: MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology
Expand Tier II Rat 860 Genes GS223141: Bone structure and strength QTL 25 (Bss25 Published QTL Chr 10)
Expand Tier II Rat 895 Genes GS224914: Blood pressure QTL 300 (Bp300 Published QTL Chr 10)
Expand Tier II Mouse 579 Genes GS129172: pregnancy QTL 2 (Pregq2 Published QTL Chr 11)
Expand Tier I Human 643 Genes GS227315: MSigDB Geneset - TGACATY_UNKNOWN
Expand Tier I Mouse MP 16 Genes GS166126: MP:0004412 abnormal cochlear microphonics
Expand Tier II Human 5070 Genes GS243926: [MeSH] Exons : D005091
Expand Tier II Human 496 Genes GS235429: [MeSH] Ear : D004423
Expand Tier I Mouse MP 6 Genes GS168036: MP:0004466 short cochlear outer hair cells
Expand Tier I Mouse GO 342 Genes GS335710: GO:0005929 cilium
Expand Tier I Human 2208 Genes GS230495: MSigDB Geneset - GGGAGGRR_V$MAZ_Q6
Expand Tier II Rat 375 Genes GS224238: Blood pressure QTL 280 (Bp280 Published QTL Chr 10)
Expand Tier I Mouse MP 3142 Genes GS169830: MP:0005384 cellular phenotype
Expand Tier I Mouse GO 3385 Genes GS335154: GO:0048731 system development
Expand Tier I Human 152 Genes GS174979: HP:0011061 Abnormality of dental structure
Expand Tier II Rat 1845 Genes GS224997: Collagen induced arthritis QTL 21 (Cia21 Published QTL Chr 10)
Expand Tier I Human CTD 4420 Genes GS124185: Plant Extracts interacting with Homo sapiens associated genes (MeSH:D010936) in CTD
Expand Tier I Human 240 Genes GS231685: PC Geneset - "V$LFA1_Q6" pathway genes
Expand Tier I Mouse GO 8920 Genes GS331753: GO:0008150 biological_process
Expand Tier I Mouse MP 458 Genes GS165253: MP:0001399 hyperactivity
Expand Tier II Human 6241 Genes GS236947: [MeSH] Brain : D001921
Expand Tier I Rat CTD 207 Genes GS264856: 1-aminocyclopentane-1,2,4-tricarboxylic acid interacting with Rattus norvegicus associated genes (MeSH:C409063) in CTD
Expand Tier II Human 17829 Genes GS235234: [MeSH] Biochemical Phenomena : D001669
Expand Tier I Mouse GO 222 Genes GS335035: GO:0007605 sensory perception of sound
Expand Tier I Human CTD 766 Genes GS251857: Air Pollutants interacting with Homo sapiens associated genes (MeSH:D000393) in CTD
Expand Tier II Rat 370 Genes GS223376: Body weight QTL 57 (Bw57 Published QTL Chr 10)
Expand Tier II Mouse 692 Genes GS135389: body growth early QTL 10 (Bgeq10, Published QTL Chr 11)
Expand Tier II Human 2992 Genes GS238716: [MeSH] Genetic Linkage : D008040
Expand Tier II Human 6978 Genes GS245264: [MeSH] Nervous System : D009420
Expand Tier II Human 400 Genes GS235765: [MeSH] Chromosomes, Human, Pair 17 : D002886
Expand Tier I Human 376 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier II Human 4853 Genes GS239764: [MeSH] Glycoproteins : D006023
Expand Tier II Human 584 Genes GS238514: [MeSH] Otorhinolaryngologic Diseases : D010038
Expand Tier II Human 17829 Genes GS238030: [MeSH] Chemical Phenomena : D055598
Expand Tier I Mouse MP 45 Genes GS166022: MP:0004408 decreased cochlear hair cell number
Expand Tier II Rat 914 Genes GS223396: Experimental allergic encephalomyelitis QTL 18 (Eae18 Published QTL Chr 10)
Expand Tier II Human 796 Genes GS235887: [MeSH] Behavior, Animal : D001522
Expand Tier I Fly GO 1434 Genes GS339904: GO:0005737 cytoplasm
Expand Tier II Human 426 Genes GS235770: [MeSH] Chromosomes, Human, Pair 10 : D002879
Expand Tier I Human 1207 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Mouse GO 733 Genes GS337938: GO:0048666 neuron development
Expand Tier I Human GO 397 Genes GS311535: GO:0008092 cytoskeletal protein binding
Expand Tier I Mouse GO 165 Genes GS333751: GO:0015629 actin cytoskeleton
Expand Tier II Rat 860 Genes GS223270: Bone structure and strength QTL 33 (Bss33 Published QTL Chr 10)
Expand Tier I Mouse GO 295 Genes GS339092: GO:0015630 microtubule cytoskeleton
Expand Tier II Human 4278 Genes GS239955: [MeSH] Amino Acid Motifs : D020816
Expand Tier I Mouse GO 297 Genes GS336221: GO:0048562 embryonic organ morphogenesis
Expand Tier I Human 637 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier II Human 1749 Genes GS239907: [MeSH] Cell Surface Extensions : D022081
Expand Tier II Human 11234 Genes GS236481: [MeSH] Enzymes : D004798
Expand Tier I Mouse MP 17 Genes GS164341: MP:0006332 abnormal cochlear potential
Expand Tier II Mouse 1003 Genes GS135818: ethanol induced thermoregulation 4 (Ethm4, Published QTL Chr 11)
Expand Tier I Mouse MP 217 Genes GS163320: MP:0000031 abnormal cochlea morphology
Expand Tier II Human 896 Genes GS240585: [MeSH] Sensory Receptor Cells : D011984
Expand Tier II Rat 860 Genes GS223539: Bone mineral density QTL 57 (Bmd57 Published QTL Chr 10)
Expand Tier I Mouse MP 2295 Genes GS165466: MP:0003632 abnormal nervous system morphology
Expand Tier II Human 2351 Genes GS237067: [MeSH] Contractile Proteins : D003285
Expand Tier II Mouse 1046 Genes GS135496: brain weight QTL 1 (Brwq1, Published QTL Chr 11)
Expand Tier II Rat 532 Genes GS223666: Body weight QTL 102 (Bw102 Published QTL Chr 10)
Expand Tier I Mouse MP 55 Genes GS166643: MP:0010055 abnormal sensory neuron physiology
Expand Tier I Mouse GO 37 Genes GS335927: GO:0060122 inner ear receptor cell stereocilium organization
Expand Tier I Mouse MP 39 Genes GS164569: MP:0003879 abnormal hair cell physiology
Expand Tier I Human GO 10738 Genes GS315285: GO:0005488 binding
Expand Tier I Human 1219 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier II Human 1171 Genes GS236935: [MeSH] Rhombencephalon : D012249
Expand Tier I Human 136 Genes GS175674: HP:0007360 Aplasia/Hypoplasia of the cerebellum
Expand Tier II Human 24 Genes GS243235: [MeSH] Labyrinth Diseases : D007759
Expand Tier II Human 1770 Genes GS244236: [MeSH] Homozygote : D006720
Expand Tier II Mouse 1046 Genes GS135528: castaneus 10 week body weight 3 (C10bw3, Published QTL Chr 11)
Expand Tier II 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 MP 146 Genes GS168193: MP:0000966 decreased sensory neuron number
Expand Tier II Human 5821 Genes GS239290: [MeSH] Cell Line, Transformed : D002461
Expand Tier I Mouse MP 79 Genes GS169795: MP:0004427 abnormal vestibular labyrinth morphology
Expand Tier I Mouse MP 169 Genes GS168066: MP:0002622 abnormal cochlear hair cell morphology
Expand Tier I Human 252 Genes GS232238: PC Geneset - "V$PAX_Q6" pathway genes
Expand Tier I Mouse MP 46 Genes GS168293: MP:0004742 abnormal vestibular system physiology
Expand Tier I Human 750 Genes GS228358: MSigDB Geneset - RNGTGGGC_UNKNOWN
Expand Tier I Human 238 Genes GS227684: MSigDB Geneset - V$LMO2COM_02
Expand Tier I Human 228 Genes GS231825: PC Geneset - "V$GATA3_01" pathway genes
Expand Tier II Human 36 Genes GS234806: [MeSH] Saccule and Utricle : D012444
Expand Tier II Human 7832 Genes GS242870: [MeSH] Polymorphism, Genetic : D011110
Expand Tier I Mouse GO 700 Genes GS333206: GO:0050877 nervous system process
Expand Tier I Human 284 Genes GS228198: MSigDB Geneset - TGATTTRY_V$GFI1_01
Expand Tier I Mouse GO 5999 Genes GS338837: GO:0005488 binding
Expand Tier II Human 14167 Genes GS240208: [MeSH] Amino Acid Sequence : D000595
Expand Tier II Human 9588 Genes GS240239: [MeSH] Sequence Homology : D017385
Expand Tier I Mouse GO 219 Genes GS333479: GO:0043583 ear development
Expand Tier I Mouse MP 614 Genes GS163226: MP:0003312 abnormal locomotor coordination
Expand Tier II Mouse 801 Genes GS136780: seizure susceptibility 3 (Szs3, Published QTL Chr 11)
Expand Tier II Rat 974 Genes GS224407: Insulin level QTL 15 (Insul15 Published QTL Chr 10)
Expand Tier II 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 16 Genes GS234393: [MeSH] Vestibular Diseases : D015837
Expand Tier II Rat 178 Genes GS224584: Oil induced arthritis QTL 6 (Oia6 Published QTL Chr 10)
Expand Tier I Mouse GO 554 Genes GS336688: GO:0005856 cytoskeleton
Expand Tier II Human 249 Genes GS238427: [MeSH] Neuroepithelial Cells : D046569
Expand Tier II Human 13572 Genes GS242639: [MeSH] Metabolic Phenomena : D055754
Expand Tier II Human 313 Genes GS244503: [MeSH] Mechanoreceptors : D008465
Expand Tier II Human 3848 Genes GS238044: [MeSH] Acid Anhydride Hydrolases : D017766
Expand Tier I Human 607 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier II Human 6336 Genes GS238872: [MeSH] Central Nervous System : D002490
Expand Tier I Human 49 Genes GS173812: HP:0000738 Hallucinations
Expand Tier I Human 413 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier II Human 3253 Genes GS234190: [MeSH] Polymers : D011108
Expand Tier I Mouse CTD 6607 Genes GS257260: Vehicle Emissions interacting with Mus musculus associated genes (MeSH:D001335) in CTD
Expand Tier II Human 3726 Genes GS244254: [MeSH] Antigens, Surface : D000954
Expand Tier I Mouse GO 3999 Genes GS333347: GO:0043229 intracellular organelle
Expand Tier I Human 1 Genes GS176230: HP:0010939 Abnormality of the nasal bone
Expand Tier II Human 16597 Genes GS235287: [MeSH] Proteins : D011506
Expand Tier I Human GO 79 Genes GS311082: GO:0050953 sensory perception of light stimulus
Expand Tier II Rat 1499 Genes GS224988: Collagen induced arthritis QTL 23 (Cia23 Published QTL Chr 10)
Expand Tier II Human 16030 Genes GS243659: [MeSH] RNA, Messenger : D012333
Expand Tier II Human 2004 Genes GS241347: [MeSH] Microfilament Proteins : D008840
Expand Tier I Mouse MP 177 Genes GS163068: MP:0000045 abnormal hair cell morphology
Expand Tier II Human 7005 Genes GS243569: [MeSH] Macromolecular Substances : D046911
Expand Tier II Rat 167 Genes GS223474: Pristane induced arthritis QTL 25 (Pia25 Published QTL Chr 10)
Expand Tier II Human 17816 Genes GS235305: [MeSH] DNA, Complementary : D018076
Expand Tier I Mouse MP 13 Genes GS164027: MP:0004814 reduced linear vestibular evoked potential
Expand Tier II Human 3924 Genes GS244610: [MeSH] Nervous System Diseases : D009422
Expand Tier I Human 1163 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier II Mouse 1060 Genes GS135973: wound healing/regeneration 10 (Heal10, Published QTL Chr 11)
Expand Tier II Human 1177 Genes GS244732: [MeSH] Protein Precursors : D011498
Expand Tier II Rat 2054 Genes GS224162: Mammary tumor resistance QTL 7 (Mamtr7 Published QTL Chr 10)
Expand Tier I Fly GO 2087 Genes GS341749: GO:0043229 intracellular organelle
Expand Tier I Human 532 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Mouse MP 253 Genes GS164126: MP:0001388 abnormal stationary movement
Expand Tier II Human 11962 Genes GS245976: [MeSH] Cellular Structures : D022082
Expand Tier II Human 13 Genes GS237994: [MeSH] Deaf-Blind Disorders : D054062
Expand Tier I Human 124 Genes GS175492: HP:0000512 Abnormal electroretinogram
Expand Tier II Rat 1941 Genes GS224152: Glucose level QTL 60 (Gluco60 Published QTL Chr 10)
Expand Tier II Mouse 715 Genes GS135815: ethanol induced ataxia 10 (Etax10, Published QTL Chr 11)
Expand Tier II Human 18212 Genes GS240572: [MeSH] DNA : D004247
Expand Tier I Human GO 10188 Genes GS308991: GO:0005515 protein binding
Expand Tier II Human 11733 Genes GS241930: [MeSH] Mutation : D009154
Expand Tier I Mouse MP 30 Genes GS165256: MP:0001395 bidirectional circling
Expand Tier II Human 2330 Genes GS242217: [MeSH] Muscle Proteins : D009124
Expand Tier I Mouse MP 31 Genes GS168879: MP:0004737 absent distortion product otoacoustic emissions
Expand Tier I Mouse MP 223 Genes GS164059: MP:0006325 impaired hearing
Expand Tier I Human GO 96 Genes GS312151: GO:0048871 multicellular organismal homeostasis
Expand Tier I Human 276 Genes GS231748: PC Geneset - "TGATTTRY_V$GFI1_01" pathway genes
Expand Tier II Human 1477 Genes GS242312: [MeSH] Extracellular Matrix Proteins : D016326
Expand Tier I Mouse GO 109 Genes GS336474: GO:0042472 inner ear morphogenesis
Expand Tier II Rat 1495 Genes GS223555: Stress response QTL 5 (Stresp5 Published QTL Chr 10)
Expand Tier II Human 16814 Genes GS235942: [MeSH] Genetic Processes : D039361
Expand Tier I Mouse GO 7482 Genes GS335497: GO:0009987 cellular process
Expand Tier I Mouse GO 86 Genes GS330888: GO:0097731 9+0 non-motile cilium
Expand Tier II Human 246 Genes GS236399: [MeSH] Consanguinity : D003241
Expand Tier I Human 384 Genes GS171708: HP:0000359 Abnormality of the inner ear
Expand Tier I Mouse GO 30 Genes GS336292: GO:0001917 photoreceptor inner segment
Expand Tier II Human 451 Genes GS237443: [MeSH] Ear, Inner : D007758
Expand Tier II Rat 373 Genes GS223102: Blood pressure QTL 149 (Bp149 Published QTL Chr 10)
Expand Tier II Rat 448 Genes GS224581: Oil induced arthritis QTL 3 (Oia3 Published QTL Chr 10)
Expand Tier I Mouse GO 55 Genes GS334926: GO:0035869 ciliary transition zone
Expand Tier I Mouse MP 3256 Genes GS169828: MP:0005386 behavior/neurological phenotype
Expand Tier II Mouse 1046 Genes GS136952: weight gain in high growth mice 7 (Wg7, Published QTL Chr 11)
Expand Tier II Human 19180 Genes GS243722: [MeSH] Genetic Structures : D040342
Expand Tier II Human 34 Genes GS238726: [MeSH] Blindness : D001766
Expand Tier II Human 17454 Genes GS241889: [MeSH] Molecular Structure : D015394
Expand Tier II Mouse 1046 Genes GS135812: estradiol regulated response QTL 3 (Estq3, Published QTL Chr 11)
Expand Tier I Rat CTD 3496 Genes GS262854: Tetrachlorodibenzodioxin interacting with Rattus norvegicus associated genes (MeSH:D013749) in CTD
Expand Tier I Mouse GO 458 Genes GS336225: GO:0048568 embryonic organ development
Expand Tier II Rat 878 Genes GS224321: Blood pressure QTL 9 (Bp9 Published QTL Chr 10)
Expand Tier I Mouse MP 786 Genes GS166244: MP:0002752 abnormal somatic nervous system morphology
Expand Tier I Mouse GO 4951 Genes GS332425: GO:0005622 intracellular
Expand Tier I Mouse GO 534 Genes GS336965: GO:0007423 sensory organ development
Expand Tier II Human 4260 Genes GS234648: [MeSH] Alleles : D000483
Expand Tier II Human 16633 Genes GS235061: [MeSH] Amino Acids, Peptides, and Proteins : D000602
Expand Tier II Human 17923 Genes GS234621: [MeSH] Chemical Actions and Uses : D020164
Expand Tier I Human 172 Genes GS227945: MSigDB Geneset - chr17q25
Expand Tier I Human 192 Genes GS230311: MSigDB Geneset - V$GATA_Q6
Expand Tier I Human GO 17 Genes GS308613: GO:0030507 spectrin binding
Expand Tier I Human 402 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier II Mouse 767 Genes GS135792: epilepsy 6 (El6, Published QTL Chr 11)
Expand Tier II Human 4897 Genes GS236231: [MeSH] Antigens : D000941
Expand Tier II Mouse 769 Genes GS84255: alcohol preference locus (Published QTL, Chr 11)
Expand Tier II Human 10170 Genes GS235056: [MeSH] Peptides : D010455
Expand Tier II Human 1992 Genes GS234965: [MeSH] Cell Adhesion Molecules : D015815
Expand Tier I Mouse GO 4257 Genes GS333351: GO:0043226 organelle
Expand Tier II Human 2806 Genes GS237404: [MeSH] Chromosomes, Human, 6-12 and X : D002906
Expand Tier I Human 202 Genes GS174764: HP:0007367 Atrophy/Degeneration affecting the central nervous system
Expand Tier I Mouse MP 2915 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 II Human 13540 Genes GS241850: [MeSH] Genetic Variation : D014644
Expand Tier I Human 164 Genes GS174994: HP:0002059 Cerebral atrophy
Expand Tier I Mouse MP 417 Genes GS164346: MP:0006335 abnormal hearing electrophysiology
Expand Tier I Human GO 39 Genes GS202686: GO:0060113 inner ear receptor cell differentiation
Expand Tier II Mouse 705 Genes GS135906: gonadal fat pad weight QTL 1 (Gfpq1, Published QTL Chr 11)
Expand Tier II Human 15098 Genes GS236076: [MeSH] Protein Conformation : D011487
Expand Tier II Rat 263 Genes GS224185: Bone mineral density QTL 16 (Bmd16 Published QTL Chr 10)
Expand Tier II Human 1136 Genes GS240265: [MeSH] Neurons, Afferent : D009475
Expand Tier I Human CTD 1467 Genes GS121243: 5-dihydrocortisone interacting with Homo sapiens associated genes (MeSH:C045993) in CTD
Expand Tier I Human 362 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Mouse GO 1151 Genes GS333348: GO:0043228 non-membrane-bounded organelle
Expand Tier I Mouse MP 2315 Genes GS169391: MP:0002066 abnormal motor capabilities/coordination/movement
Expand Tier I Human 110 Genes GS230191: MSigDB Geneset - V$MEIS1AHOXA9_01
Expand Tier II Mouse 705 Genes GS136357: novelty/stress induced locomotor activation 8 (Nsila8, Published QTL Chr 11)
Expand Tier I Human 1288 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Mouse MP 889 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 Human 2115 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 511 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier II Mouse 697 Genes GS136957: weight 5 (Wght5, Published QTL Chr 11)
Expand Tier I Fly GO 3148 Genes GS343489: GO:0005575 cellular_component
Expand Tier II Human 4886 Genes GS241960: [MeSH] Protein Structure, Secondary : D017433
Expand Tier I Rat CTD 457 Genes GS266484: 2,2',3',4,4',5-hexachlorobiphenyl interacting with Rattus norvegicus associated genes (MeSH:C029790) in CTD
Expand Tier I Human GO 61 Genes GS314675: GO:0050954 sensory perception of mechanical stimulus
Expand Tier II Human 17259 Genes GS239769: [MeSH] Gene Library : D015723
Expand Tier II Mouse 1281 Genes GS129115: collagen induced arthritis 40 (Cia40 Published QTL Chr 11)
Expand Tier II Human 16451 Genes GS242107: [MeSH] Chemical Processes : D055599
Expand Tier II Human 15903 Genes GS243578: [MeSH] Reading Frames : D016364
Expand Tier I Fly GO 407 Genes GS344270: GO:0012505 endomembrane system
Expand Tier II Mouse 981 Genes GS136789: tail length QTL 8 (Tailq8, Published QTL Chr 11)
Expand Tier II Human 11159 Genes GS237597: [MeSH] Cell Physiological Processes : D055648
Expand Tier I Mouse MP 10 Genes GS163543: MP:0004431 abnormal hair cell mechanoelectric transduction
Expand Tier II Rat 1859 Genes GS224636: Cardiac mass QTL 31 (Cm31 Published QTL Chr 10)
Expand Tier I Mouse MP 735 Genes GS164023: MP:0001961 abnormal reflex
Expand Tier I Mouse GO 7487 Genes GS331100: GO:0003674 molecular_function
Expand Tier II Mouse 792 Genes GS136831: TNF-induced lethal shock susceptibility 2 (Tilss2, Published QTL Chr 11)
Expand Tier I Mouse MP 8 Genes GS167119: MP:0004577 abnormal cochlear hair cell inter-stereocilial links morphology
Expand Tier I Mouse MP 425 Genes GS166123: MP:0002102 abnormal ear morphology
Expand Tier II Human 3173 Genes GS241597: [MeSH] Disease Models, Animal : D004195
Expand Tier II Human 9485 Genes GS235276: [MeSH] Signal Transduction : D015398
Expand Tier II Rat 974 Genes GS223703: Serum leptin concentration QTL 8 (Slep8 Published QTL Chr 10)
Expand Tier II Human 3927 Genes GS234354: [MeSH] Cytoskeletal Proteins : D003598
Expand Tier I Human 2365 Genes GS175529: HP:0000001 All
Expand Tier II Human 1666 Genes GS240069: [MeSH] Microtubule Proteins : D008868
Expand Tier I Rat CTD 954 Genes GS266866: 1-indanol interacting with Rattus norvegicus associated genes (MeSH:C016515) in CTD
Expand Tier I Mouse GO 6332 Genes GS332424: GO:0005623 cell
Expand Tier I Mouse MP 19 Genes GS167591: MP:0004330 abnormal vestibular saccular macula morphology
Expand Tier I Fly GO 2128 Genes GS341752: GO:0043226 organelle
Expand Tier II Human 661 Genes GS238687: [MeSH] Disease : D004194
Expand Tier I Human CTD 119 Genes GS124572: fluoranthene interacting with Homo sapiens associated genes (MeSH:C007738) in CTD
Expand Tier II Human 646 Genes GS235519: [MeSH] Syndrome : D013577
Expand Tier I Mouse GO 4889 Genes GS332814: GO:0044424 intracellular part
Expand Tier I Mouse MP 60 Genes GS165854: MP:0004406 abnormal cochlear hair cell number
Expand Tier I Fly GO 177 Genes GS342081: GO:0097708 intracellular vesicle
Expand Tier II Rat 957 Genes GS224788: Bone structure and strength QTL 79 (Bss79 Published QTL Chr 10)
Expand Tier II Human 18339 Genes GS238575: [MeSH] Nucleic Acids : D009696
Expand Tier I Mouse GO 2684 Genes GS337474: GO:0048513 animal organ development
Expand Tier II Human 1600 Genes GS237854: [MeSH] Peripheral Nervous System : D017933
Expand Tier II Human 5577 Genes GS238961: [MeSH] Nerve Tissue Proteins : D009419
Expand Tier I Fly GO 1036 Genes GS343445: GO:0044444 cytoplasmic part
Expand Tier I Mouse GO 272 Genes GS328161: GO:0090596 sensory organ morphogenesis
Expand Tier II Human 874 Genes GS238245: [MeSH] Cerebellum : D002531
Expand Tier II Mouse 735 Genes GS135274: "alcohol preference locus 18, male specific" (Alcp18, Published QTL Chr 11)
Expand Tier I Human 514 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Mouse GO 927 Genes GS333481: GO:0030182 neuron differentiation
Expand Tier I Human GO 15 Genes GS307771: GO:0045494 photoreceptor cell maintenance
Expand Tier I Mouse GO 564 Genes GS334421: GO:0043005 neuron projection
Expand Tier I Mouse MP 58 Genes GS168880: MP:0004736 abnormal distortion product otoacoustic emission
Expand Tier II Rat 1341 Genes GS224784: Carrageenan-induced inflammation QTL 1 (Cari1 Published QTL Chr 10)
Expand Tier I Mouse MP 154 Genes GS163724: MP:0000436 abnormal head movements
Expand Tier I Mouse GO 1517 Genes GS332025: GO:0007399 nervous system development
Expand Tier II Human 17884 Genes GS239502: [MeSH] Nucleic Acid Probes : D015341
Expand Tier I Mouse GO 222 Genes GS331227: GO:0042803 protein homodimerization activity
Expand Tier II Human 8777 Genes GS244835: [MeSH] Chromosomes : D002875
Expand Tier II Human 2091 Genes GS237069: [MeSH] Congenital Abnormalities : D000013
Expand Tier II Rat 1737 Genes GS223978: Pristane induced arthritis QTL 10 (Pia10 Published QTL Chr 10)
Expand Tier I Mouse MP 38 Genes GS163695: MP:0006090 abnormal utricle morphology
Expand Tier I Human 918 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human GO 762 Genes GS310374: GO:0042592 homeostatic process
Expand Tier I Human 604 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier II Human 15271 Genes GS242059: [MeSH] Cells : D002477
Expand Tier I Human 88 Genes GS173329: HP:0000682 Abnormality of dental enamel
Expand Tier II Rat 401 Genes GS223064: Mammary carcinoma susceptibility QTL 15 (Mcs15 Published QTL Chr 10)
Expand Tier II Human 1432 Genes GS239652: [MeSH] Genes, Recessive : D005808
Expand Tier II Human 102 Genes GS238585: [MeSH] Retinitis Pigmentosa : D012174
Expand Tier II Human 1611 Genes GS238953: [MeSH] Neurologic Manifestations : D009461
Expand Tier I Fly GO 177 Genes GS342208: GO:0031410 cytoplasmic vesicle
Expand Tier I Mouse GO 954 Genes GS330762: GO:0120025 plasma membrane bounded cell projection
Expand Tier I Mouse GO 55 Genes GS336570: GO:0060119 inner ear receptor cell development
Expand Tier II Rat 974 Genes GS224708: Serum cholesterol level QTL 65 (Scl65 Published QTL Chr 10)
Expand Tier II Human 18365 Genes GS244482: [MeSH] Nucleic Acids, Nucleotides, and Nucleosides : D009706
Expand Tier I Fly GO 106 Genes GS346826: GO:0005768 endosome
Expand Tier I Human GO 61 Genes GS311209: GO:0007605 sensory perception of sound
Expand Tier I Mouse GO 458 Genes GS338151: GO:0044430 cytoskeletal part
Expand Tier I Mouse MP 17 Genes GS166929: MP:0004333 abnormal utricular macula morphology
Expand Tier I Rat CTD 237 Genes GS267129: 2,5,2',5'-tetrachlorobiphenyl interacting with Rattus norvegicus associated genes (MeSH:C009407) in CTD
Expand Tier I Mouse GO 841 Genes GS332956: GO:0030030 cell projection organization
Expand Tier I Mouse MP 31 Genes GS165664: MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles
Expand Tier I Mouse GO 619 Genes GS337135: GO:0044463 cell projection part
Expand Tier I Mouse MP 72 Genes GS166904: MP:0001485 abnormal pinna reflex
Expand Tier I Mouse GO 1039 Genes GS332771: GO:0009790 embryo development
Expand Tier II Human 8178 Genes GS243735: [MeSH] Biological Factors : D001685
Expand Tier I Human 170 Genes GS173476: HP:0002311 Incoordination
Expand Tier I Mouse GO 63 Genes GS334506: GO:0036064 ciliary basal body
Expand Tier I Human GO 8 Genes GS209985: GO:0050957 equilibrioception
Expand Tier II Human 17873 Genes GS235797: [MeSH] DNA Probes : D015342
Expand Tier I Mouse MP 66 Genes GS168762: MP:0005423 abnormal somatic nervous system physiology
Expand Tier II Rat 1737 Genes GS224614: Adjuvant induced arthritis QTL 5 (Aia5 Published QTL Chr 10)
Expand Tier II Human 5214 Genes GS242147: [MeSH] Fibroblasts : D005347
Expand Tier I Mouse GO 153 Genes GS338750: GO:0005815 microtubule organizing center
Expand Tier I Mouse MP 1583 Genes GS165465: MP:0003633 abnormal nervous system physiology
Expand Tier II Human 11214 Genes GS242332: [MeSH] Cell Physiological Phenomena : D002468
Expand Tier I Human 387 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier II Rat 811 Genes GS223260: Neuroinflammation QTL 7 (Neuinf7 Published QTL Chr 10)
Expand Tier II Human 68 Genes GS237886: [MeSH] Vision Disorders : D014786
Expand Tier II Human 16448 Genes GS235242: [MeSH] Biochemical Processes : D055438
Expand Tier II Rat 931 Genes GS224933: Adjuvant induced arthritis QTL 19 (Aia19 Published QTL Chr 10)
Expand Tier II Human 16145 Genes GS245685: [MeSH] RNA : D012313
Expand Tier I Human 52 Genes GS174577: HP:0009924 Aplasia/Hypoplasia involving the nose
Expand Tier I Mouse GO 1151 Genes GS336502: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier I Fly GO 1724 Genes GS341751: GO:0043227 membrane-bounded organelle
Expand Tier I Human CTD 3575 Genes GS124427: butyraldehyde interacting with Homo sapiens associated genes (MeSH:C018475) in CTD
Expand Tier II Human 3057 Genes GS235557: [MeSH] Animal Diseases : D000820
Expand Tier I Mouse MP 24 Genes GS163528: MP:0004434 abnormal cochlear outer hair cell physiology
Expand Tier I Human 2195 Genes GS232290: PC Geneset - "GGGAGGRR_V$MAZ_Q6" pathway genes
Expand Tier I Human GO 190 Genes GS311212: GO:0007600 sensory perception
Expand Tier I Mouse MP 46 Genes GS163980: MP:0006089 abnormal vestibular saccule morphology
Expand Tier I Mouse GO 35 Genes GS338422: GO:0032391 photoreceptor connecting cilium
Expand Tier I Human 231 Genes GS227927: MSigDB Geneset - V$GATA3_01
Expand Tier I Mouse GO 128 Genes GS336471: GO:0042471 ear morphogenesis
Expand Tier I Human 34 Genes GS172732: HP:0001751 Vestibular dysfunction
Expand Tier I Mouse GO 4903 Genes GS335881: GO:0032501 multicellular organismal process
Expand Tier I Human 268 Genes GS229238: MSigDB Geneset - YKACATTT_UNKNOWN
Expand Tier II Rat 234 Genes GS223760: Collagen induced arthritis QTL 5 (Cia5 Published QTL Chr 10)
Expand Tier I Mouse GO 735 Genes GS329544: GO:0097458 neuron part
Expand Tier I Human CTD 1467 Genes GS123541: pentanal interacting with Homo sapiens associated genes (MeSH:C046012) in CTD
Expand Tier I Human GO 22 Genes GS313316: GO:0001895 retina homeostasis
Expand Tier II Human 13275 Genes GS238592: [MeSH] Cells, Cultured : D002478
Expand Tier I Human 42 Genes GS174449: HP:0001123 Visual field defect
Expand Tier I Human 412 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human 135 Genes GS232407: PC Geneset - "V$MEIS1BHOXA9_01" pathway genes
Expand Tier I Human 1563 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human CTD 3849 Genes GS252195: (+)-JQ1 compound interacting with Homo sapiens associated genes (MeSH:C561695) in CTD
Expand Tier I Mouse GO 5381 Genes GS332861: GO:0005515 protein binding
Expand Tier II Rat 618 Genes GS223217: Glomerulus QTL 25 (Glom25 Published QTL Chr 10)
Expand Tier II Human 6771 Genes GS237257: [MeSH] Pathologic Processes : D010335
Expand Tier I Fly GO 2449 Genes GS341210: GO:0044424 intracellular part
Expand Tier I Human 139 Genes GS230584: MSigDB Geneset - V$MEIS1BHOXA9_01
Expand Tier II Mouse 1003 Genes GS136677: skull morphology 16 (Skull16, Published QTL Chr 11)
Expand Tier II Mouse 1038 Genes GS136434: pulmonary adenoma susceptibility 5b (Pas5b, Published QTL Chr 11)
Expand Tier II Human 1285 Genes GS234181: [MeSH] Retina : D012160
Expand Tier I Human 463 Genes GS232087: PC Geneset - "TCANNTGAY_V$SREBP1_01" pathway genes
Expand Tier II Rat 113 Genes GS223390: Experimental allergic encephalomyelitis QTL 12 (Eae12 Published QTL Chr 10)
Expand Tier I Mouse MP 14 Genes GS162966: MP:0004324 vestibular hair cell degeneration
Expand Tier II Human 9890 Genes GS235538: [MeSH] Protein Binding : D011485
Expand Tier I Human 1 Genes GS173492: HP:0004646 Hypoplasia of the nasal bone
Expand Tier II Human 3607 Genes GS243780: [MeSH] COS Cells : D019556
Expand Tier II Human 5776 Genes GS235960: [MeSH] Connective Tissue Cells : D003239
Expand Tier I Mouse MP 134 Genes GS169847: MP:0004399 abnormal cochlear outer hair cell morphology
Expand Tier II Human 4645 Genes GS238960: [MeSH] Membrane Glycoproteins : D008562
Expand Tier I Mouse MP 579 Genes GS167922: MP:0000959 abnormal somatic sensory system morphology
Expand Tier II Human 1449 Genes GS242366: [MeSH] Inheritance Patterns : D040582
Expand Tier II Human 761 Genes GS236992: [MeSH] Chromosomes, Human, 16-18 : D002902
Expand Tier II Human 4038 Genes GS235744: [MeSH] Neurons : D009474
Expand Tier I Mouse MP 302 Genes GS165390: MP:0003224 neuron degeneration
Expand Tier II Human 1978 Genes GS239789: [MeSH] Adenosine Triphosphatases : D000251
Expand Tier I Mouse GO 4215 Genes GS335880: GO:0032502 developmental process
Expand Tier I Mouse CTD 4083 Genes GS257019: Dietary Fats interacting with Mus musculus associated genes (MeSH:D004041) in CTD
Expand Tier II Rat 1387 Genes GS224316: Blood pressure QTL 1 (Bp1 Published QTL Chr 10)
Expand Tier II Mouse 710 Genes GS136328: non-insulin-dependent diabetes mellitus 4 (Nidd4, Published QTL Chr 11)
Expand Tier I Human 194 Genes GS232060: PC Geneset - "V$GATA_Q6" pathway genes
Expand Tier I Rat CTD 2821 Genes GS263731: Crotalid Venoms interacting with Rattus norvegicus associated genes (MeSH:D003435) in CTD
Expand Tier I Human GO 1243 Genes GS307397: GO:0042802 identical protein binding
Expand Tier II Human 17895 Genes GS243866: [MeSH] Laboratory Chemicals : D019995
Expand Tier I Mouse GO 194 Genes GS331629: GO:0048839 inner ear development
Expand Tier II Rat 967 Genes GS224952: CIA Autoantibody QTL 2 (Ciaa2 Published QTL Chr 10)
Expand Tier I Human 740 Genes GS228632: MSigDB Geneset - CTGCAGY_UNKNOWN
Expand Tier I Human 93 Genes GS176289: HP:0002120 Cerebral cortical atrophy
Expand Tier I Human GO 1934 Genes GS307919: GO:0065008 regulation of biological quality
Expand Tier I Human CTD 1807 Genes GS126601: Aluminum interacting with nan associated genes (MeSH:D000535) in CTD
Expand Tier I Mouse MP 11231 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier II Human 9296 Genes GS237836: [MeSH] Carrier Proteins : D002352
Expand Tier II Human 1544 Genes GS237303: [MeSH] Mutation, Missense : D020125
Expand Tier I Mouse GO 963 Genes GS337159: GO:0042995 cell projection
Expand Tier II Human 17896 Genes GS243233: [MeSH] Specialty Uses of Chemicals : D020313
Expand Tier II Human 7086 Genes GS239275: [MeSH] Intracellular Signaling Peptides and Proteins : D047908
Expand Tier II Human 199 Genes GS243183: [MeSH] Hearing Loss : D034381
Expand Tier II Human 1445 Genes GS235299: [MeSH] Physical Processes : D055586
Expand Tier II Rat 856 Genes GS223659: Body weight QTL 106 (Bw106 Published QTL Chr 10)
Expand Tier I Mouse MP 74 Genes GS165873: MP:0004404 cochlear outer hair cell degeneration
Expand Tier I Human GO 181 Genes GS313508: GO:0060249 anatomical structure homeostasis
Expand Tier I Human 1 Genes GS171749: HP:0010937 Abnormality of the nasal skeleton
Expand Tier I Mouse MP 41 Genes GS168065: MP:0002623 abnormal vestibular hair cell morphology
Expand Tier I Human 1099 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier II Human 313 Genes GS235047: [MeSH] Retinal Degeneration : D012162
Expand Tier I Human 66 Genes GS173753: HP:0000510 Retinitis pigmentosa
Expand Tier I Mouse MP 7 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 14808 Genes GS236241: [MeSH] Protein Structure, Tertiary : D017434
Expand Tier II Mouse 792 Genes GS136514: protein kinase C content in lungs (Pkccl, Published QTL Chr 11)
Expand Tier I Mouse GO 619 Genes GS328786: GO:0120038 plasma membrane bounded cell projection part
Expand Tier I Mouse GO 5871 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Mouse MP 16 Genes GS163829: MP:0011060 abnormal kinocilium morphology
Expand Tier II Human 1782 Genes GS241289: [MeSH] Behavior : D001519
Expand Tier I Human CTD 3187 Genes GS124951: Atrazine interacting with Homo sapiens associated genes (MeSH:D001280) in CTD
Expand Tier I Mouse GO 1907 Genes GS337230: GO:0009653 anatomical structure morphogenesis
Expand Tier I Mouse MP 82 Genes GS165787: MP:0001522 impaired swimming
Expand Tier II Human 911 Genes GS234220: [MeSH] Metencephalon : D020540
Expand Tier I Mouse GO 263 Genes GS334922: GO:0044441 ciliary part
Expand Tier I Human 235 Genes GS232281: PC Geneset - "V$LMO2COM_02" pathway genes
Expand Tier II 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 I Human 188 Genes GS174247: HP:0000539 Abnormality of refraction
Expand Tier I Mouse MP 73 Genes GS167643: MP:0000034 abnormal inner ear vestibule morphology
Expand Tier II Human 3949 Genes GS240624: [MeSH] Adaptor Proteins, Signal Transducing : D048868
Expand Tier II Human 3681 Genes GS234179: [MeSH] DNA, Intergenic : D021901
Expand Tier I Human 1056 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 243 Genes GS229555: MSigDB Geneset - V$LFA1_Q6
Expand Tier I Mouse GO 3974 Genes GS337870: GO:0048856 anatomical structure development
Expand Tier I Mouse MP 113 Genes GS168215: MP:0001967 deafness
Expand Tier I Human 698 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier II Human 238 Genes GS237228: [MeSH] Eye Diseases, Hereditary : D015785
Expand Tier II Human 1360 Genes GS236633: [MeSH] Brain Stem : D001933
Expand Tier I Mouse MP 33 Genes GS167452: MP:0004532 abnormal inner hair cell stereociliary bundle morphology
Expand Tier II Human 3527 Genes GS237484: [MeSH] Congenital, Hereditary, and Neonatal Diseases and Abnormalities : D009358
Expand Tier II Human 18573 Genes GS238415: [MeSH] Genome Components : D040481
Expand Tier I Human 838 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier II Human 1048 Genes GS240795: [MeSH] Eye Diseases : D005128
Expand Tier I Human 111 Genes GS228993: MSigDB Geneset - CCANNAGRKGGC_UNKNOWN
Expand Tier II Human 892 Genes GS243817: [MeSH] Abnormalities, Multiple : D000015
Expand Tier II Human 1643 Genes GS237070: [MeSH] Biophysical Phenomena : D055592
Expand Tier I Rat CTD 207 Genes GS264855: PCB 180 interacting with Rattus norvegicus associated genes (MeSH:C410127) in CTD
Expand Tier I Human GO 5595 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Mouse GO 7187 Genes GS334959: GO:0005575 cellular_component
Expand Tier I Mouse MP 1422 Genes GS165260: MP:0001392 abnormal locomotor behavior
Expand Tier II Human 15107 Genes GS238930: [MeSH] Molecular Conformation : D008968
Expand Tier II Human 17884 Genes GS240750: [MeSH] Molecular Probes : D015335
Expand Tier I Mouse GO 6323 Genes GS337136: GO:0044464 cell part
Expand Tier II Rat 1737 Genes GS223091: Collagen induced arthritis QTL 20 (Cia20 Published QTL Chr 10)
Expand Tier I Mouse GO 1120 Genes GS333851: GO:0022008 neurogenesis
Expand Tier I Mouse MP 174 Genes GS163498: MP:0003308 abnormal cochlear sensory epithelium morphology
Expand Tier I Mouse MP 104 Genes GS169841: MP:0004393 abnormal cochlear inner hair cell morphology
Expand Tier II Rat 775 Genes GS224389: Pancreatic morphology QTL 2 (Pancm2 Published QTL Chr 10)
Expand Tier I Mouse MP 355 Genes GS165385: MP:0008946 abnormal neuron number
Expand Tier I Mouse GO 2697 Genes GS334419: GO:0030154 cell differentiation
Expand Tier II Human 2729 Genes GS234130: [MeSH] Genetic Diseases, Inborn : D030342
Expand Tier II Human 2232 Genes GS236425: [MeSH] Signs and Symptoms : D012816
Expand Tier I Human 458 Genes GS229382: MSigDB Geneset - TCANNTGAY_V$SREBP1_01
Expand Tier I Mouse GO 827 Genes GS328788: GO:0120036 plasma membrane bounded cell projection organization