Gene Details



USH1G and homologs in 7 species are found in 613 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 II Mouse 1003 Genes GS136433: pulmonary adenoma susceptibility 5a (Pas5a, Published QTL Chr 11)
Expand Tier II Human 455 Genes GS237881: [MeSH] Retinal Diseases : D012164
Expand Tier II Human 9028 Genes GS241666: [MeSH] Sequence Homology, Amino Acid : D017386
Expand Tier II Rat 167 Genes GS224097: Collagen induced arthritis QTL 28 (Cia28 Published QTL Chr 10)
Expand Tier II Human 8283 Genes GS245646: [MeSH] Hydrolases : D006867
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 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 II Human 125 Genes GS236163: [MeSH] Deafness : D003638
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 I Mouse GO 3705 Genes GS188641: GO:0071944 cell periphery
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 496 Genes GS235429: [MeSH] Ear : D004423
Expand Tier II Human 5070 Genes GS243926: [MeSH] Exons : D005091
Expand Tier I Mouse MP 6 Genes GS168036: MP:0004466 short cochlear outer hair cells
Expand Tier I Mouse GO 13255 Genes GS178461: GO:0009987 cellular process
Expand Tier I Human 2208 Genes GS230495: MSigDB Geneset - GGGAGGRR_V$MAZ_Q6
Expand Tier II Rat 375 Genes GS224238: Blood pressure QTL 280 (Bp280 Published QTL Chr 10)
Expand Tier I Mouse MP 3142 Genes GS169830: MP:0005384 cellular phenotype
Expand Tier II Rat 1845 Genes GS224997: Collagen induced arthritis QTL 21 (Cia21 Published QTL Chr 10)
Expand Tier I Human 152 Genes GS174979: HP:0011061 Abnormality of dental structure
Expand Tier I Human 240 Genes GS231685: PC Geneset - "V$LFA1_Q6" pathway genes
Expand Tier I Human CTD 4420 Genes GS124185: Plant Extracts interacting with Homo sapiens associated genes (MeSH:D010936) in CTD
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 I Mouse GO 453 Genes GS181012: GO:0007423 sensory organ development
Expand Tier II Human 17829 Genes GS235234: [MeSH] Biochemical Phenomena : D001669
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 I Mouse GO 22753 Genes GS193268: GO:0005575 cellular_component
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 I Mouse GO 123 Genes GS193046: GO:0050953 sensory perception of light stimulus
Expand Tier II Human 6978 Genes GS245264: [MeSH] Nervous System : D009420
Expand Tier I Human GO 563 Genes GS194646: GO:0042803 protein homodimerization activity
Expand Tier II Human 400 Genes GS235765: [MeSH] Chromosomes, Human, Pair 17 : D002886
Expand Tier II Human 4853 Genes GS239764: [MeSH] Glycoproteins : D006023
Expand Tier I Human 376 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier II Human 17829 Genes GS238030: [MeSH] Chemical Phenomena : D055598
Expand Tier II Human 584 Genes GS238514: [MeSH] Otorhinolaryngologic Diseases : D010038
Expand Tier I Human GO 2649 Genes GS207797: GO:0030154 cell differentiation
Expand Tier I Mouse MP 45 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 4064 Genes GS207581: GO:0007275 multicellular organismal development
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 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 Human GO 4016 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier II Rat 860 Genes GS223270: Bone structure and strength QTL 33 (Bss33 Published QTL Chr 10)
Expand Tier II Human 4278 Genes GS239955: [MeSH] Amino Acid Motifs : D020816
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 Rat 860 Genes GS223539: Bone mineral density QTL 57 (Bmd57 Published QTL Chr 10)
Expand Tier II Human 896 Genes GS240585: [MeSH] Sensory Receptor Cells : D011984
Expand Tier I Mouse GO 187 Genes GS187229: GO:0043583 ear development
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 MP 39 Genes GS164569: MP:0003879 abnormal hair cell physiology
Expand Tier II Human 1171 Genes GS236935: [MeSH] Rhombencephalon : D012249
Expand Tier I Human 1219 Genes GS170964: HP:0000152 Abnormality of head and neck
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 I Mouse GO 13184 Genes GS191106: GO:0044464 cell part
Expand Tier II Human 1770 Genes GS244236: [MeSH] Homozygote : D006720
Expand Tier I Mouse GO 8406 Genes GS177404: GO:0005737 cytoplasm
Expand Tier I Mouse GO 3492 Genes GS177570: GO:0016043 cellular component organization
Expand Tier I Mouse GO 3076 Genes GS177265: GO:0048731 system development
Expand Tier I Human GO 1786 Genes GS208893: GO:0005856 cytoskeleton
Expand Tier I Human GO 12166 Genes GS201251: GO:0044424 intracellular part
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 Mouse GO 3614 Genes GS178359: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human 590 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human GO 204 Genes GS210485: GO:0007601 visual perception
Expand Tier I Mouse MP 146 Genes GS168193: MP:0000966 decreased sensory neuron number
Expand Tier I Mouse GO 3592 Genes GS188142: GO:0048856 anatomical structure development
Expand Tier II Human 5821 Genes GS239290: [MeSH] Cell Line, Transformed : D002461
Expand Tier I Mouse MP 169 Genes GS168066: MP:0002622 abnormal cochlear hair cell morphology
Expand Tier I Mouse MP 79 Genes GS169795: MP:0004427 abnormal vestibular labyrinth morphology
Expand Tier I Human 252 Genes GS232238: PC Geneset - "V$PAX_Q6" pathway genes
Expand Tier I Mouse MP 46 Genes GS168293: MP:0004742 abnormal vestibular system physiology
Expand Tier I Human 238 Genes GS227684: MSigDB Geneset - V$LMO2COM_02
Expand Tier I Human 750 Genes GS228358: MSigDB Geneset - RNGTGGGC_UNKNOWN
Expand Tier I Human 228 Genes GS231825: PC Geneset - "V$GATA3_01" pathway genes
Expand Tier II Human 36 Genes GS234806: [MeSH] Saccule and Utricle : D012444
Expand Tier I Mouse GO 347 Genes GS181267: GO:0048568 embryonic organ development
Expand Tier II Human 7832 Genes GS242870: [MeSH] Polymorphism, Genetic : D011110
Expand Tier I Human 284 Genes GS228198: MSigDB Geneset - TGATTTRY_V$GFI1_01
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 II Mouse 801 Genes GS136780: seizure susceptibility 3 (Szs3, Published QTL Chr 11)
Expand Tier I Mouse MP 614 Genes GS163226: MP:0003312 abnormal locomotor coordination
Expand Tier II Rat 974 Genes GS224407: Insulin level QTL 15 (Insul15 Published QTL Chr 10)
Expand Tier I Human GO 4344 Genes GS205500: GO:0071944 cell periphery
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 Human GO 38 Genes GS198664: GO:0043954 cellular component maintenance
Expand Tier II Human 249 Genes GS238427: [MeSH] Neuroepithelial Cells : D046569
Expand Tier II Human 13572 Genes GS242639: [MeSH] Metabolic Phenomena : D055754
Expand Tier I Human GO 493 Genes GS209225: GO:0007600 sensory perception
Expand Tier II Human 3848 Genes GS238044: [MeSH] Acid Anhydride Hydrolases : D017766
Expand Tier II Human 313 Genes GS244503: [MeSH] Mechanoreceptors : D008465
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 6336 Genes GS238872: [MeSH] Central Nervous System : D002490
Expand Tier I Human 49 Genes GS173812: HP:0000738 Hallucinations
Expand Tier I Human GO 434 Genes GS197802: GO:0007423 sensory organ development
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 GO 911 Genes GS179236: GO:0048699 generation of neurons
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 Human GO 216 Genes GS198051: GO:0048562 embryonic organ morphogenesis
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 898 Genes GS201125: GO:0009790 embryo development
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 Rat 167 Genes GS223474: Pristane induced arthritis QTL 25 (Pia25 Published QTL Chr 10)
Expand Tier II Human 7005 Genes GS243569: [MeSH] Macromolecular Substances : D046911
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 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 253 Genes GS164126: MP:0001388 abnormal stationary movement
Expand Tier II Human 11962 Genes GS245976: [MeSH] Cellular Structures : D022082
Expand Tier II Rat 1941 Genes GS224152: Glucose level QTL 60 (Gluco60 Published QTL Chr 10)
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 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 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 223 Genes GS164059: MP:0006325 impaired hearing
Expand Tier I Mouse MP 31 Genes GS168879: MP:0004737 absent distortion product otoacoustic emissions
Expand Tier I Mouse MP 29 Genes GS165729: MP:0002730 head shaking
Expand Tier II Human 15903 Genes GS234668: [MeSH] Open Reading Frames : D016366
Expand Tier II Human 1995 Genes GS242610: [MeSH] Sense Organs : D012679
Expand Tier I Human GO 3117 Genes GS197892: GO:0043228 non-membrane-bounded organelle
Expand Tier I Human 276 Genes GS231748: PC Geneset - "TGATTTRY_V$GFI1_01" pathway genes
Expand Tier I Human GO 6743 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier II Human 1477 Genes GS242312: [MeSH] Extracellular Matrix Proteins : D016326
Expand Tier I Human 1204 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier II Rat 1495 Genes GS223555: Stress response QTL 5 (Stresp5 Published QTL Chr 10)
Expand Tier II Human 16814 Genes GS235942: [MeSH] Genetic Processes : D039361
Expand Tier II Human 7665 Genes GS238111: [MeSH] Genotype : D005838
Expand Tier I Mouse MP 52 Genes GS169793: MP:0004425 abnormal otolith organ morphology
Expand Tier I Human GO 25 Genes GS203824: GO:0045494 photoreceptor cell maintenance
Expand Tier II Human 2529 Genes GS241608: [MeSH] Haplotypes : D006239
Expand Tier I Mouse GO 902 Genes GS184317: GO:0009790 embryo development
Expand Tier II Human 246 Genes GS236399: [MeSH] Consanguinity : D003241
Expand Tier I Human GO 5627 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 252 Genes GS229583: MSigDB Geneset - V$PAX_Q6
Expand Tier I Human 384 Genes GS171708: HP:0000359 Abnormality of the inner ear
Expand Tier I Mouse GO 9739 Genes GS186744: GO:0043226 organelle
Expand Tier II Human 108 Genes GS234972: [MeSH] Vestibule, Labyrinth : D014722
Expand Tier I Human GO 1691 Genes GS209960: GO:0003008 system process
Expand Tier I Mouse MP 20 Genes GS165864: MP:0004405 absent cochlear hair cells
Expand Tier II Rat 373 Genes GS223102: Blood pressure QTL 149 (Bp149 Published QTL Chr 10)
Expand Tier II Human 451 Genes GS237443: [MeSH] Ear, Inner : D007758
Expand Tier II Rat 448 Genes GS224581: Oil induced arthritis QTL 3 (Oia3 Published QTL Chr 10)
Expand Tier I Mouse MP 3256 Genes GS169828: MP:0005386 behavior/neurological phenotype
Expand Tier I Rat CTD 2821 Genes GS263730: Cuprizone interacting with Rattus norvegicus associated genes (MeSH:D003471) in CTD
Expand Tier I Mouse MP 176 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 941 Genes GS168958: MP:0003492 abnormal involuntary movement
Expand Tier I Mouse GO 11363 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 II Human 11267 Genes GS239295: [MeSH] Enzymes and Coenzymes : D045762
Expand Tier II Human 305 Genes GS236348: [MeSH] Cochlea : D003051
Expand Tier II Mouse 700 Genes GS136632: small effect CIA locus 6 (Secia6, Published QTL Chr 11)
Expand Tier II Mouse 1046 Genes GS136952: weight gain in high growth mice 7 (Wg7, Published QTL Chr 11)
Expand Tier II Human 148 Genes GS237293: [MeSH] Hair Cells, Auditory : D006198
Expand Tier II Human 34 Genes GS238726: [MeSH] Blindness : D001766
Expand Tier II Human 19180 Genes GS243722: [MeSH] Genetic Structures : D040342
Expand Tier I Mouse GO 159 Genes GS179560: GO:0048839 inner ear development
Expand Tier II Human 17816 Genes GS241744: [MeSH] DNA, Single-Stranded : D004277
Expand Tier I Human CTD 5430 Genes GS127127: Benzo(a)pyrene interacting with Homo sapiens associated genes (MeSH:D001564) in CTD
Expand Tier II Human 17454 Genes GS241889: [MeSH] Molecular Structure : D015394
Expand Tier II Mouse 714 Genes GS135555: CD8 memory T cell subset 4 (Cd8mts4, Published QTL Chr 11)
Expand Tier II Rat 1499 Genes GS223083: Collagen induced arthritis QTL 22 (Cia22 Published QTL Chr 10)
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 II Mouse 792 Genes GS136220: mandible length 12 (Manln12, Published QTL Chr 11)
Expand Tier II Rat 878 Genes GS224321: Blood pressure QTL 9 (Bp9 Published QTL Chr 10)
Expand Tier II Rat 461 Genes GS224585: Oil induced arthritis QTL 5 (Oia5 Published QTL Chr 10)
Expand Tier II Human 654 Genes GS238802: [MeSH] Molecular Motor Proteins : D020409
Expand Tier I Mouse MP 786 Genes GS166244: MP:0002752 abnormal somatic nervous system morphology
Expand Tier I Human 1489 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier II Human 4260 Genes GS234648: [MeSH] Alleles : D000483
Expand Tier I Human GO 15161 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 9089 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human GO 2047 Genes GS203406: GO:0009653 anatomical structure morphogenesis
Expand Tier I Human GO 182 Genes GS204087: GO:0043583 ear development
Expand Tier I Mouse MP 13 Genes GS164584: MP:0004331 vestibular saccular macula degeneration
Expand Tier I Mouse MP 59 Genes GS164345: MP:0006336 abnormal otoacoustic response
Expand Tier I Mouse MP 20 Genes GS170320: MP:0004813 absent linear vestibular evoked potential
Expand Tier I Mouse GO 22332 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Human 172 Genes GS227945: MSigDB Geneset - chr17q25
Expand Tier II Human 17923 Genes GS234621: [MeSH] Chemical Actions and Uses : D020164
Expand Tier II Human 16633 Genes GS235061: [MeSH] Amino Acids, Peptides, and Proteins : D000602
Expand Tier I Mouse MP 1030 Genes GS163227: MP:0003313 abnormal locomotor activation
Expand Tier I Human GO 10565 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human 192 Genes GS230311: MSigDB Geneset - V$GATA_Q6
Expand Tier II Human 18556 Genes GS245795: [MeSH] Genes : D005796
Expand Tier I Mouse GO 1465 Genes GS180001: GO:0048646 anatomical structure formation involved in morphogenesis
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 I Human 202 Genes GS171631: HP:0008051 Abnormality of the retinal pigment epithelium
Expand Tier I Human 341 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier II Mouse 769 Genes GS84255: alcohol preference locus (Published QTL, Chr 11)
Expand Tier I Human CTD 3575 Genes GS255189: Bisecurin I interacting with Homo sapiens associated genes (MeSH:C018467) in CTD
Expand Tier II Mouse 1003 Genes GS135678: compensatory renal hypertrophy QTL 1 (Crhq1, Published QTL Chr 11)
Expand Tier I Mouse MP 29 Genes GS164033: MP:0004812 abnormal linear vestibular evoked potential
Expand Tier I Rat CTD 954 Genes GS266865: indole-3-carbinol interacting with Rattus norvegicus associated genes (MeSH:C016517) in CTD
Expand Tier I Mouse MP 74 Genes GS165663: MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology
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 2706 Genes GS192471: GO:0048869 cellular developmental process
Expand Tier II Human 15970 Genes GS237679: [MeSH] Genetic Code : D005815
Expand Tier I Mouse MP 394 Genes GS165985: MP:0000965 abnormal sensory neuron morphology
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 289 Genes GS167105: MP:0008948 decreased neuron number
Expand Tier I Human GO 4087 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Mouse MP 203 Genes GS165114: MP:0004426 abnormal cochlear labyrinth morphology
Expand Tier I Mouse MP 2915 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier II Human 13379 Genes GS240987: [MeSH] Metabolism : D008660
Expand Tier I Human 1 Genes GS171027: HP:0010940 Aplasia/Hypoplasia of the nasal bone
Expand Tier I Human 2330 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 356 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier II Human 109 Genes GS239631: [MeSH] Mechanotransduction, Cellular : D040542
Expand Tier II Human 13540 Genes GS241850: [MeSH] Genetic Variation : D014644
Expand Tier II Human 177 Genes GS243045: [MeSH] Dyneins : D004398
Expand Tier I Human 164 Genes GS174994: HP:0002059 Cerebral atrophy
Expand Tier II Mouse 707 Genes GS83981: cocaine related behavior 12 (Cocrb12, Published QTL, Chr 11)
Expand Tier I Mouse MP 417 Genes GS164346: MP:0006335 abnormal hearing electrophysiology
Expand Tier II Human 161 Genes GS243224: [MeSH] Organ of Corti : D009925
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 I Mouse GO 24 Genes GS186963: GO:0045494 photoreceptor cell maintenance
Expand Tier I Human 164 Genes GS227333: MSigDB Geneset - V$SREBP1_01
Expand Tier II Rat 263 Genes GS224185: Bone mineral density QTL 16 (Bmd16 Published QTL Chr 10)
Expand Tier II Human 15098 Genes GS236076: [MeSH] Protein Conformation : D011487
Expand Tier I Mouse GO 49 Genes GS185850: GO:0060113 inner ear receptor cell differentiation
Expand Tier II Human 1136 Genes GS240265: [MeSH] Neurons, Afferent : D009475
Expand Tier I Human 289 Genes GS227399: MSigDB Geneset - GATAAGR_V$GATA_C
Expand Tier I Mouse MP 90 Genes GS165544: MP:0004362 cochlear hair cell degeneration
Expand Tier I Mouse MP 739 Genes GS164724: MP:0001516 abnormal motor coordination/ balance
Expand Tier I Human CTD 1467 Genes GS121243: 5-dihydrocortisone interacting with Homo sapiens associated genes (MeSH:C045993) in CTD
Expand Tier I Human 362 Genes GS173991: HP:0000505 Visual impairment
Expand Tier II Mouse 692 Genes GS136896: visual placing (Vispl, Published QTL Chr 11)
Expand Tier I Mouse MP 2315 Genes GS169391: MP:0002066 abnormal motor capabilities/coordination/movement
Expand Tier I Human 110 Genes GS230191: MSigDB Geneset - V$MEIS1AHOXA9_01
Expand Tier II Mouse 705 Genes GS136357: novelty/stress induced locomotor activation 8 (Nsila8, Published QTL Chr 11)
Expand Tier II Rat 950 Genes GS224939: Schwannoma susceptibility QTL 1 (Schws1 Published QTL Chr 10)
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 II Rat 957 Genes GS224069: Bone structure and strength QTL 80 (Bss80 Published QTL Chr 10)
Expand Tier II Rat 302 Genes GS224134: Blood pressure QTL 310 (Bp310 Published QTL Chr 10)
Expand Tier II Human 99 Genes GS235739: [MeSH] Hearing Loss, Sensorineural : D006319
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 Mouse MP 193 Genes GS165391: MP:0000972 abnormal mechanoreceptor morphology
Expand Tier II Human 10111 Genes GS235272: [MeSH] Membrane Proteins : D008565
Expand Tier I Human 541 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 469 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Mouse GO 10875 Genes GS181473: GO:0005488 binding
Expand Tier I Mouse GO 580 Genes GS177903: GO:0042803 protein homodimerization activity
Expand Tier I Human 2115 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 180 Genes GS232370: PC Geneset - "V$SREBP1_01" pathway genes
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 Mouse GO 5884 Genes GS180036: GO:0032501 multicellular organismal process
Expand Tier I Mouse GO 824 Genes GS187237: GO:0030182 neuron differentiation
Expand Tier I Mouse MP 1557 Genes GS168956: MP:0003491 abnormal voluntary movement
Expand Tier I Mouse GO 8142 Genes GS190714: GO:0016020 membrane
Expand Tier II Human 7335 Genes GS243335: [MeSH] Chromosomes, Mammalian : D033481
Expand Tier I Human GO 7725 Genes GS207616: GO:0016020 membrane
Expand Tier II Human 6299 Genes GS242721: [MeSH] Physical Phenomena : D055585
Expand Tier II Human 266 Genes GS244540: [MeSH] Lod Score : D008126
Expand Tier II Human 4886 Genes GS241960: [MeSH] Protein Structure, Secondary : D017433
Expand Tier I Human GO 12781 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse GO 3613 Genes GS180229: GO:0005886 plasma membrane
Expand Tier I Human GO 1722 Genes GS198004: GO:0007399 nervous system development
Expand Tier I Mouse GO 4068 Genes GS180034: GO:0032502 developmental process
Expand Tier I Human GO 4203 Genes GS195112: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human GO 113 Genes GS197510: GO:0042471 ear morphogenesis
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 II Human 17259 Genes GS239769: [MeSH] Gene Library : D015723
Expand Tier II Rat 263 Genes GS225009: Bone structure and strength QTL 18 (Bss18 Published QTL Chr 10)
Expand Tier II Human 12777 Genes GS238348: [MeSH] Cell Line : D002460
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 347 Genes GS243624: [MeSH] Cilia : D002923
Expand Tier II Human 15903 Genes GS243578: [MeSH] Reading Frames : D016364
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 1026 Genes GS169225: MP:0000358 abnormal cell morphology
Expand Tier I Human GO 3507 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 234 Genes GS163316: MP:0000035 abnormal membranous labyrinth morphology
Expand Tier II Rat 975 Genes GS224571: Bone structure and strength QTL 6 (Bss6 Published QTL Chr 10)
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 II Mouse 697 Genes GS136244: methamphetamine response QTL 3 (Marq3, Published QTL Chr 11)
Expand Tier II Mouse 792 Genes GS136831: TNF-induced lethal shock susceptibility 2 (Tilss2, Published QTL Chr 11)
Expand Tier II Human 3217 Genes GS239332: [MeSH] Biopolymers : D001704
Expand Tier I Human 41 Genes GS176115: HP:0000540 Hypermetropia
Expand Tier II Human 19359 Genes GS241072: [MeSH] Genetic Phenomena : D055614
Expand Tier I Human GO 156 Genes GS196324: GO:0048839 inner ear development
Expand Tier I Human GO 11880 Genes GS198263: GO:0005488 binding
Expand Tier II Human 16876 Genes GS243325: [MeSH] Base Sequence : D001483
Expand Tier I Mouse GO 87 Genes GS188110: GO:0050905 neuromuscular process
Expand Tier II Human 101 Genes GS234599: [MeSH] Retinal Dystrophies : D058499
Expand Tier I Mouse MP 8 Genes GS167119: MP:0004577 abnormal cochlear hair cell inter-stereocilial links morphology
Expand Tier II Human 381 Genes GS244927: [MeSH] Myosins : D009218
Expand Tier I Human 188 Genes GS171512: HP:0007703 Abnormal retinal pigmentation
Expand Tier II Mouse 981 Genes GS135755: experimental allergic encephalomyelitis susceptibility 22 (Eae22, Published QTL Chr 11)
Expand Tier I Mouse MP 425 Genes GS166123: MP:0002102 abnormal ear morphology
Expand Tier II Human 7110 Genes GS241292: [MeSH] Pathological Conditions, Signs and Symptoms : D013568
Expand Tier II Human 3173 Genes GS241597: [MeSH] Disease Models, Animal : D004195
Expand Tier I Human 413 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier II Human 9485 Genes GS235276: [MeSH] Signal Transduction : D015398
Expand Tier I Mouse GO 2134 Genes GS186067: GO:0050877 neurological system process
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 Human 368 Genes GS170971: HP:0000407 Sensorineural hearing impairment
Expand Tier I Rat CTD 954 Genes GS266866: 1-indanol interacting with Rattus norvegicus associated genes (MeSH:C016515) in CTD
Expand Tier I Mouse MP 19 Genes GS167591: MP:0004330 abnormal vestibular saccular macula morphology
Expand Tier I Human 1261 Genes GS229869: MSigDB Geneset - TATAAA_V$TATA_01
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 I Mouse GO 2494 Genes GS193018: GO:0003008 system process
Expand Tier II Mouse 792 Genes GS135341: atherosclerosis 19 (Ath19, Published QTL Chr 11)
Expand Tier I Mouse MP 202 Genes GS167140: MP:0003169 abnormal scala media morphology
Expand Tier I Mouse GO 112 Genes GS180713: GO:0042471 ear morphogenesis
Expand Tier II Rat 811 Genes GS223460: Mammary carcinoma susceptibility QTL 7 (Mcs7 Published QTL Chr 10)
Expand Tier II Human 646 Genes GS235519: [MeSH] Syndrome : D013577
Expand Tier I Mouse MP 60 Genes GS165854: MP:0004406 abnormal cochlear hair cell number
Expand Tier I Mouse GO 933 Genes GS178813: GO:0046983 protein dimerization activity
Expand Tier II Rat 957 Genes GS224788: Bone structure and strength QTL 79 (Bss79 Published QTL Chr 10)
Expand Tier I Mouse GO 11123 Genes GS184447: GO:0044424 intracellular part
Expand Tier II Human 18339 Genes GS238575: [MeSH] Nucleic Acids : D009696
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 Human GO 1135 Genes GS205691: GO:0022008 neurogenesis
Expand Tier II Human 874 Genes GS238245: [MeSH] Cerebellum : D002531
Expand Tier I Mouse GO 8 Genes GS193044: GO:0050957 equilibrioception
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 Human GO 964 Genes GS195570: GO:0046983 protein dimerization activity
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 II Human 17884 Genes GS239502: [MeSH] Nucleic Acid Probes : D015341
Expand Tier I Human GO 2540 Genes GS203335: GO:0048513 organ development
Expand Tier I Mouse GO 55 Genes GS188801: GO:0042490 mechanoreceptor differentiation
Expand Tier I Mouse GO 9716 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Mouse GO 22819 Genes GS180164: GO:0008150 biological_process
Expand Tier II Human 8777 Genes GS244835: [MeSH] Chromosomes : D002875
Expand Tier II Rat 1737 Genes GS223978: Pristane induced arthritis QTL 10 (Pia10 Published QTL Chr 10)
Expand Tier II Human 2091 Genes GS237069: [MeSH] Congenital Abnormalities : D000013
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 604 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human GO 492 Genes GS201848: GO:0048598 embryonic morphogenesis
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 Human GO 1586 Genes GS196772: GO:0048646 anatomical structure formation involved in morphogenesis
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 Mouse GO 1849 Genes GS186562: GO:0009653 anatomical structure morphogenesis
Expand Tier I Mouse MP 17 Genes GS166929: MP:0004333 abnormal utricular macula morphology
Expand Tier I Human GO 14550 Genes GS208012: GO:0044464 cell part
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 MP 31 Genes GS165664: MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles
Expand Tier I Mouse MP 72 Genes GS166904: MP:0001485 abnormal pinna reflex
Expand Tier I Human GO 16873 Genes GS210212: GO:0005575 cellular_component
Expand Tier II Human 8178 Genes GS243735: [MeSH] Biological Factors : D001685
Expand Tier I Human 170 Genes GS173476: HP:0002311 Incoordination
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 MP 1583 Genes GS165465: MP:0003633 abnormal nervous system physiology
Expand Tier I Mouse GO 226 Genes GS181262: GO:0048562 embryonic organ morphogenesis
Expand Tier II Rat 811 Genes GS223260: Neuroinflammation QTL 7 (Neuinf7 Published QTL Chr 10)
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 Human 16448 Genes GS235242: [MeSH] Biochemical Processes : D055438
Expand Tier II Human 68 Genes GS237886: [MeSH] Vision Disorders : D014786
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 Human GO 205 Genes GS209987: GO:0050953 sensory perception of light stimulus
Expand Tier II Human 3057 Genes GS235557: [MeSH] Animal Diseases : D000820
Expand Tier I Human CTD 3575 Genes GS124427: butyraldehyde interacting with Homo sapiens associated genes (MeSH:C018475) in CTD
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$MAZ_Q6" pathway genes
Expand Tier I Human GO 75 Genes GS204969: GO:0050905 neuromuscular process
Expand Tier I Mouse MP 46 Genes GS163980: MP:0006089 abnormal vestibular saccule morphology
Expand Tier I Mouse GO 132 Genes GS193043: GO:0050954 sensory perception of mechanical stimulus
Expand Tier I Human 231 Genes GS227927: MSigDB Geneset - V$GATA3_01
Expand Tier I Human 34 Genes GS172732: HP:0001751 Vestibular dysfunction
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 Human CTD 1467 Genes GS123541: pentanal interacting with Homo sapiens associated genes (MeSH:C046012) in CTD
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 135 Genes GS232407: PC Geneset - "V$MEIS1BHOXA9_01" pathway genes
Expand Tier I Human 412 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human 1563 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human CTD 3849 Genes GS252195: (+)-JQ1 compound interacting with Homo sapiens associated genes (MeSH:C561695) in CTD
Expand Tier II Rat 618 Genes GS223217: Glomerulus QTL 25 (Glom25 Published QTL Chr 10)
Expand Tier II Human 6771 Genes GS237257: [MeSH] Pathologic Processes : D010335
Expand Tier I Human 139 Genes GS230584: MSigDB Geneset - V$MEIS1BHOXA9_01
Expand Tier II Mouse 1003 Genes GS136677: skull morphology 16 (Skull16, Published QTL Chr 11)
Expand Tier I Mouse GO 863 Genes GS177902: GO:0042802 identical protein binding
Expand Tier I Mouse GO 13185 Genes GS182834: GO:0005623 cell
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 GO 1066 Genes GS196002: GO:0048699 generation of neurons
Expand Tier I Human 463 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 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 I Mouse GO 2876 Genes GS182474: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier II Human 5776 Genes GS235960: [MeSH] Connective Tissue Cells : D003239
Expand Tier II Human 3607 Genes GS243780: [MeSH] COS Cells : D019556
Expand Tier I Human GO 12490 Genes GS199635: GO:0005622 intracellular