Gene Details



USH1G and homologs in 1 species are found in 131 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 Human GO 4554 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human GO 75 Genes GS204969: GO:0050905 neuromuscular process
Expand Tier I Human 803 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human 124 Genes GS175492: HP:0000512 Abnormal electroretinogram
Expand Tier I Human GO 10576 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 3116 Genes GS197892: GO:0043228 non-membrane-bounded organelle
Expand Tier I Human GO 6743 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human 1203 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 34 Genes GS172732: HP:0001751 Vestibular dysfunction
Expand Tier I Human GO 7609 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human GO 25 Genes GS203824: GO:0045494 photoreceptor cell maintenance
Expand Tier I Human 42 Genes GS174449: HP:0001123 Visual field defect
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 Human 411 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human GO 1691 Genes GS209960: GO:0003008 system process
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 168 Genes GS175668: HP:0007369 Atrophy/Degeneration affecting the cerebrum
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 15151 Genes GS194087: GO:0003674 molecular_function
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 GO 182 Genes GS204087: GO:0043583 ear development
Expand Tier I Human 152 Genes GS174979: HP:0011061 Abnormality of dental structure
Expand Tier I Human GO 1066 Genes GS196002: GO:0048699 generation of neurons
Expand Tier I Human GO 329 Genes GS198056: GO:0048568 embryonic organ development
Expand Tier I Human 837 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 4338 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Human 1 Genes GS173492: HP:0004646 Hypoplasia of the nasal bone
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 401 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Human 342 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human 201 Genes GS171631: HP:0008051 Abnormality of the retinal pigment epithelium
Expand Tier I Human 341 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 1135 Genes GS205691: GO:0022008 neurogenesis
Expand Tier I Human GO 38 Genes GS198664: GO:0043954 cellular component maintenance
Expand Tier I Human GO 493 Genes GS209225: GO:0007600 sensory perception
Expand Tier I Human GO 2364 Genes GS207365: GO:0005829 cytosol
Expand Tier I Human 513 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human 607 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human GO 565 Genes GS194646: GO:0042803 protein homodimerization activity
Expand Tier I Human GO 966 Genes GS195570: GO:0046983 protein dimerization activity
Expand Tier I Human GO 132 Genes GS209984: GO:0050954 sensory perception of mechanical stimulus
Expand Tier I Human 202 Genes GS174764: HP:0007367 Atrophy/Degeneration affecting the central nervous system
Expand Tier I Human 49 Genes GS173812: HP:0000738 Hallucinations
Expand Tier I Human GO 4085 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human 375 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Human GO 2539 Genes GS203335: GO:0048513 organ development
Expand Tier I Human GO 2653 Genes GS207797: GO:0030154 cell differentiation
Expand Tier I Human 1 Genes GS171027: HP:0010940 Aplasia/Hypoplasia of the nasal bone
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
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 I Human GO 856 Genes GS194645: GO:0042802 identical protein binding
Expand Tier I Human GO 124 Genes GS210482: GO:0007605 sensory perception of sound
Expand Tier I Human 356 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Human GO 4061 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human 917 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 164 Genes GS174994: HP:0002059 Cerebral atrophy
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 I Human GO 39 Genes GS202686: GO:0060113 inner ear receptor cell differentiation
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 I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human GO 1587 Genes GS196772: GO:0048646 anatomical structure formation involved in morphogenesis
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 I Human 93 Genes GS176289: HP:0002120 Cerebral cortical atrophy
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human GO 898 Genes GS201125: GO:0009790 embryo development
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human 361 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human 636 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 170 Genes GS173476: HP:0002311 Incoordination
Expand Tier I Human GO 45 Genes GS197327: GO:0050885 neuromuscular process controlling balance
Expand Tier I Human GO 45 Genes GS205662: GO:0042490 mechanoreceptor differentiation
Expand Tier I Human GO 8 Genes GS209985: GO:0050957 equilibrioception
Expand Tier I Human GO 4250 Genes GS197009: GO:0005886 plasma membrane
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
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 386 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 1235 Genes GS202899: GO:0050877 neurological system process
Expand Tier I Human 469 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human GO 792 Genes GS205616: GO:0009887 organ morphogenesis
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 576 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human 532 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human 52 Genes GS174577: HP:0009924 Aplasia/Hypoplasia involving the nose
Expand Tier I Human 510 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Human GO 205 Genes GS209987: GO:0050953 sensory perception of light stimulus
Expand Tier I Human 1 Genes GS171749: HP:0010937 Abnormality of the nasal skeleton
Expand Tier I Human GO 7308 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 66 Genes GS173753: HP:0000510 Retinitis pigmentosa
Expand Tier I Human GO 7717 Genes GS207616: GO:0016020 membrane
Expand Tier I Human 413 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human GO 1722 Genes GS198004: GO:0007399 nervous system development
Expand Tier I Human GO 2816 Genes GS209411: GO:0048869 cellular developmental process
Expand Tier I Human GO 4201 Genes GS195112: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human GO 113 Genes GS197510: GO:0042471 ear morphogenesis
Expand Tier I Human 136 Genes GS175674: HP:0007360 Aplasia/Hypoplasia of the cerebellum
Expand Tier I Human GO 363 Genes GS205224: GO:0015629 actin cytoskeleton
Expand Tier I Human GO 1786 Genes GS208893: GO:0005856 cytoskeleton
Expand Tier I Human GO 95 Genes GS197513: GO:0042472 inner ear morphogenesis
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human GO 3506 Genes GS193991: GO:0048731 system development
Expand Tier I Human 590 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human 381 Genes GS175714: HP:0011389 Functional abnormality of the inner ear
Expand Tier I Human GO 204 Genes GS210485: GO:0007601 visual perception
Expand Tier I Human 95 Genes GS176616: HP:0000662 Night blindness
Expand Tier I Human 187 Genes GS174247: HP:0000539 Abnormality of refraction
Expand Tier I Human 40 Genes GS176115: HP:0000540 Hypermetropia
Expand Tier I Human GO 156 Genes GS196324: GO:0048839 inner ear development
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 187 Genes GS171512: HP:0007703 Abnormal retinal pigmentation
Expand Tier I Human GO 985 Genes GS204095: GO:0030182 neuron differentiation
Expand Tier I Human 413 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 368 Genes GS170971: HP:0000407 Sensorineural hearing impairment
Expand Tier I Human GO 3116 Genes GS199272: GO:0043232 intracellular non-membrane-bounded organelle