Gene Details



USH2A and homologs in 7 species are found in 472 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 I Human 385 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Mouse GO 335 Genes GS193273: GO:0005578 proteinaceous extracellular matrix
Expand Tier I Mouse 291 Genes GS136389: autoimmune orchitis resistance 4 (Orch4, Published QTL Chr 1)
Expand Tier II Mouse 161 Genes GS35309: Whole Brain Gene expression correlates of Acoustic Startle Response Percentage of maximum startle response at 80 db in Females & Males BXD
Expand Tier I Human 877 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Mouse MP 1698 Genes GS164220: MP:0002882 abnormal neuron morphology
Expand Tier I Mouse MP 279 Genes GS163596: MP:0000026 abnormal inner ear morphology
Expand Tier I Human GO 7609 Genes GS201949: GO:0044699 single-organism process
Expand Tier III Human 49 Genes GS221924: Capture panel of retinitis pigmentosa (RP) genes used to diagnose Chinese probands
Expand Tier I Human GO 224 Genes GS210290: GO:0016324 apical plasma membrane
Expand Tier I Mouse GO 3706 Genes GS188641: GO:0071944 cell periphery
Expand Tier I Mouse 465 Genes GS136446: pentobarbital withdrawal QTL 1 (Pbw1, Published QTL Chr 1)
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Human 152 Genes GS174979: HP:0011061 Abnormality of dental structure
Expand Tier I Mouse MP 388 Genes GS170108: MP:0003727 abnormal retinal layer morphology
Expand Tier I Mouse 465 Genes GS136573: radiation-induced acute myeloid leukemia sensitivity 1 (Ramls1, Published QTL Chr 1)
Expand Tier I Mouse GO 454 Genes GS181012: GO:0007423 sensory organ development
Expand Tier I Mouse 385 Genes GS135862: femur breaking strength 5 (Fembrs5, Published QTL Chr 1)
Expand Tier III Rat 367 Genes GS224153: Glucose level QTL 63 (Gluco63 Published QTL Chr 13)
Expand Tier I Mouse MP 182 Genes GS163581: MP:0001004 abnormal retinal photoreceptor morphology
Expand Tier I Mouse 385 Genes GS135953: HDL QTL 20 (Hdlq20, Published QTL Chr 1)
Expand Tier I Mouse MP 190 Genes GS166394: MP:0003728 abnormal retinal photoreceptor layer morphology
Expand Tier I Mouse GO 2678 Genes GS181892: GO:0048523 negative regulation of cellular process
Expand Tier I Mouse GO 23778 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Mouse 465 Genes GS135270: alcohol dependency 1 (Alcdp1, Published QTL Chr 1)
Expand Tier I Mouse 454 Genes GS135788: ethanol induced locomotor activity 1 (Eila1, Published QTL Chr 1)
Expand Tier I Mouse GO 123 Genes GS193046: GO:0050953 sensory perception of light stimulus
Expand Tier I Human 375 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Human GO 2653 Genes GS207797: GO:0030154 cell differentiation
Expand Tier I Mouse GO 1 Genes GS188339: GO:0060171 stereocilium membrane
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 I Human 120 Genes GS172358: HP:0003117 Abnormality of circulating hormone level
Expand Tier I Mouse MP 47 Genes GS164793: MP:0008587 short photoreceptor outer segment
Expand Tier I Human 156 Genes GS172363: HP:0004324 Increased body weight
Expand Tier I Human 598 Genes GS176718: HP:0000078 Abnormality of the genital system
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 II Mouse 435 Genes GS83986: cocaine related behavior 2 (Cocrb2, Published QTL, Chr 1)
Expand Tier II Mouse 399 Genes GS84113: differences in cocaine responsiveness (Published QTL, Chr 1)
Expand Tier I Mouse GO 5734 Genes GS190713: GO:0016021 integral to membrane
Expand Tier I Human 636 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human GO 121 Genes GS200823: GO:0009913 epidermal cell differentiation
Expand Tier I Mouse 460 Genes GS135464: blood pressure QTL 21 (Bpq21, Published QTL Chr 1)
Expand Tier I Mouse MP 228 Genes GS163320: MP:0000031 abnormal cochlea morphology
Expand Tier I Human 140 Genes GS174906: HP:0000545 Myopia
Expand Tier I Human 423 Genes GS175332: HP:0000032 Abnormality of male external genitalia
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 I Human 323 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier I Human GO 4 Genes GS198531: GO:0002139 stereocilia coupling link
Expand Tier I Human 12 Genes GS171801: HP:0008527 Congenital sensorineural hearing impairment
Expand Tier I Mouse GO 28 Genes GS181577: GO:0017022 myosin binding
Expand Tier I Human GO 2 Genes GS205196: GO:0060171 stereocilium membrane
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier II Mouse 399 Genes GS84111: differences in cocaine responsiveness (Published QTL, Chr 1)
Expand Tier I Human 136 Genes GS175674: HP:0007360 Aplasia/Hypoplasia of the cerebellum
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 736 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Mouse GO 2994 Genes GS186215: GO:0048519 negative regulation of biological process
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 12162 Genes GS201251: GO:0044424 intracellular part
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 I Human 16 Genes GS175180: HP:0011073 Abnormality of dental color
Expand Tier I Mouse MP 171 Genes GS168066: MP:0002622 abnormal cochlear hair cell morphology
Expand Tier II Mouse 27 Genes GS35554: Neocortex Gene expression correlates of Morphine photocell counts minutes 120-135 in Males BXD
Expand Tier I Human GO 1006 Genes GS196988: GO:0045595 regulation of cell differentiation
Expand Human 167 Genes GS222318: Coding region point mutations in ASD probands.
Expand Tier I Human 389 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Mouse MP 95 Genes GS166313: MP:0008450 retinal photoreceptor degeneration
Expand Tier I Human GO 4338 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Human 342 Genes GS174378: HP:0000518 Cataract
Expand Human 70 Genes GS222261: Genes associated with retinitis pigmentosa (RP) on OMIM database
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 Mouse 295 Genes GS136536: promotion susceptibility QTL 3 (Psl3, Published QTL Chr 1)
Expand Tier I Mouse 460 Genes GS136188: lipoprotein QTL 3 (Lprq3, Published QTL Chr 1)
Expand Human 70 Genes GS221898: RetNet genes linked to retinitis pigmentosa (RP)
Expand Tier II Mouse 366 Genes GS84115: morphine preference (Published QTL, Chr 1)
Expand Tier I Human 607 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human GO 5 Genes GS194007: GO:0048496 maintenance of organ identity
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 I Mouse GO 912 Genes GS179236: GO:0048699 generation of neurons
Expand Tier II Mouse 161 Genes GS35289: Whole Brain Gene expression correlates of Prepulse inhibition at 80db in Females & Males BXD
Expand Tier I Mouse 325 Genes GS136699: systematic lupus erythematosus susceptibility 1c (Sle1c, Published QTL Chr 1)
Expand Tier I Human GO 6 Genes GS205287: GO:0035315 hair cell differentiation
Expand Tier I Mouse MP 323 Genes GS163432: MP:0006069 abnormal retinal neuronal layer morphology
Expand Tier I Human 103 Genes GS173741: HP:0100699 Scarring
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 GS186488: GO:0048513 organ development
Expand Tier I Human 397 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Mouse MP 328 Genes GS168218: MP:0001963 abnormal hearing physiology
Expand Tier I Mouse MP 178 Genes GS163068: MP:0000045 abnormal hair cell morphology
Expand Tier I Human GO 453 Genes GS194627: GO:0008544 epidermis development
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 Mouse 466 Genes GS136839: trypansomiasis infection response 3c (Tir3c, Published QTL Chr 1)
Expand Tier I Mouse MP 384 Genes GS164570: MP:0003878 abnormal ear physiology
Expand Tier I Human 79 Genes GS175373: HP:0011486 Abnormality of corneal thickness
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 III Rat 555 Genes GS223140: Bone structure and strength QTL 26 (Bss26 Published QTL Chr 13)
Expand Tier I Human 489 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Human 435 Genes GS173024: HP:0000811 Abnormal external genitalia
Expand Tier I Mouse GO 10 Genes GS185806: GO:0031528 microvillus membrane
Expand Tier I Human GO 4554 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human GO 1430 Genes GS206618: GO:0050793 regulation of developmental process
Expand Tier I Mouse MP 32 Genes GS168863: MP:0004402 decreased cochlear outer hair cell number
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 Mouse GO 1398 Genes GS181215: GO:0007399 nervous system development
Expand Tier I Human GO 2112 Genes GS210214: GO:0005576 extracellular region
Expand Tier I Human GO 10576 Genes GS203594: GO:0043226 organelle
Expand Tier I Mouse GO 244 Genes GS179362: GO:0005929 cilium
Expand Tier I Mouse GO 377 Genes GS179537: GO:0031012 extracellular matrix
Expand Tier I Mouse GO 4 Genes GS181740: GO:0002139 stereocilia coupling link
Expand Tier I Mouse 454 Genes GS136703: systematic lupus erythematosus susceptibility 9 (Sle9, Published QTL Chr 1)
Expand Tier I Human 532 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier I Human GO 3116 Genes GS197892: GO:0043228 non-membrane-bounded organelle
Expand Tier I Mouse 465 Genes GS136008: haloperidol induced catalepsy 2 (Hpic2, Published QTL Chr 1)
Expand Tier I Human 1203 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human GO 25 Genes GS203824: GO:0045494 photoreceptor cell maintenance
Expand Tier II Mouse 338 Genes GS84320: pentobarbital withdrawal on Chr1 (Published QTL)
Expand Tier I Mouse 465 Genes GS135534: caffeine metabolism QTL 1 (Cafq1, Published QTL Chr 1)
Expand Tier I Mouse GO 87 Genes GS190034: GO:0031513 nonmotile primary cilium
Expand Tier I Mouse GO 1440 Genes GS181988: GO:0044459 plasma membrane part
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 Human 74 Genes GS222884: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PEROXISOME
Expand Tier I Mouse MP 553 Genes GS167217: MP:0001325 abnormal retina morphology
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Human GO 1905 Genes GS198782: GO:0044459 plasma membrane part
Expand Tier I Human GO 1691 Genes GS209960: GO:0003008 system process
Expand Tier I Human 177 Genes GS171047: HP:0008736 Hypoplasia of penis
Expand Tier I Mouse MP 180 Genes GS163063: MP:0000042 abnormal organ of Corti morphology
Expand Tier I Human 274 Genes GS172372: HP:0000648 Optic atrophy
Expand Tier I Human 168 Genes GS175668: HP:0007369 Atrophy/Degeneration affecting the cerebrum
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier I Mouse GO 2876 Genes GS181102: GO:0043228 non-membrane-bounded organelle
Expand Tier I Mouse GO 123 Genes GS193540: GO:0007601 visual perception
Expand Tier I Mouse GO 188 Genes GS184450: GO:0044420 extracellular matrix part
Expand Tier I Mouse GO 159 Genes GS179560: GO:0048839 inner ear development
Expand Tier III Mouse 6189 Genes GS213074: Genes with suggestive difference in (B6PF1) vs (PB6F1 + B6 + PWD) comparison
Expand Tier I Mouse 454 Genes GS136969: Y-linked autoimmune acceleration 4 (Yaa4, Published QTL Chr 1)
Expand Tier I Mouse GO 293 Genes GS192775: GO:0045177 apical part of cell
Expand Tier I Human 169 Genes GS173988: HP:0000501 Glaucoma
Expand Tier I Mouse GO 441 Genes GS180207: GO:0045596 negative regulation of cell differentiation
Expand Tier I Mouse GO 5859 Genes GS182404: GO:0031224 intrinsic to membrane
Expand Tier I Human 248 Genes GS176844: HP:0000429 Abnormality of the nasal alae
Expand Tier I Mouse 454 Genes GS135994: hippocampal weight 1 (Hipp1, Published QTL Chr 1)
Expand Tier I Human GO 634 Genes GS194613: GO:0008092 cytoskeletal protein binding
Expand Tier III Mouse 85 Genes GS34589: Striatum Gene expression correlates of Novel environment distance (cm) travelled minutes 0-15 in BXD Males
Expand Tier II Mouse 399 Genes GS84112: differences in cocaine responsiveness (Published QTL, Chr 1)
Expand Tier I Mouse MP 959 Genes GS166244: MP:0002752 abnormal somatic nervous system morphology
Expand Tier II Mouse 56 Genes GS84121: METH responses for body temperature (Published QTL, Chr 1)
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Mouse GO 5 Genes GS177280: GO:0048496 maintenance of organ identity
Expand Tier I Human GO 2828 Genes GS198684: GO:0048523 negative regulation of cellular process
Expand Tier I Human GO 8094 Genes GS202316: GO:0050789 regulation of biological process
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 280 Genes GS176231: HP:0010938 Abnormality of the external nose
Expand Tier I Human GO 182 Genes GS204087: GO:0043583 ear development
Expand Tier I Human GO 361 Genes GS210217: GO:0005578 proteinaceous extracellular matrix
Expand Tier I Human 100 Genes GS176744: HP:0000987 Atypical scarring of skin
Expand Tier I Human GO 186 Genes GS201254: GO:0044420 extracellular matrix part
Expand Tier I Human GO 535 Genes GS205331: GO:0051093 negative regulation of developmental process
Expand Tier I Mouse MP 52 Genes GS164345: MP:0006336 abnormal otoacoustic response
Expand Tier I Mouse 351 Genes GS136291: modifier of obesity related sterility 1 (Mors1, Published QTL Chr 1)
Expand Tier I Human 89 Genes GS176988: HP:0008046 Abnormality of the retinal vasculature
Expand Tier I Mouse GO 406 Genes GS182368: GO:0043025 neuronal cell body
Expand Tier I Mouse GO 23359 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Human GO 5243 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Mouse 465 Genes GS135552: CD8 T memory cell subset 1 (Cd8mts1, Published QTL Chr 1)
Expand Tier I Mouse MP 17 Genes GS163030: MP:0008582 short photoreceptor inner segment
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier III Rat 866 Genes GS223219: Glomerulus QTL 27 (Glom27 Published QTL Chr 13)
Expand Tier I Mouse GO 605 Genes GS177870: GO:0008092 cytoskeletal protein binding
Expand Tier I Human 401 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Mouse 431 Genes GS135596: cholesterol and HDL QTL 1 (Chldq1, Published QTL Chr 1)
Expand Tier I Human GO 16 Genes GS202642: GO:0031528 microvillus membrane
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 Mouse 465 Genes GS135344: atherosclerosis 9 (Ath9, Published QTL Chr 1)
Expand Tier III Human 1 Genes GS221923: Multiplex ligation-dependent probe amplification (MLPA) and array-based comparative genomic hybridization (aCGH) used to study mutations in USH2A gene that cause retinitis pigmentosa (RP)
Expand Human 74 Genes GS221263: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PEROXISOME
Expand Tier I Mouse GO 6473 Genes GS184448: GO:0044425 membrane part
Expand Tier I Mouse MP 51 Genes GS165924: MP:0004400 abnormal cochlear outer hair cell number
Expand Tier I Human 171 Genes GS173019: HP:0000819 Diabetes mellitus
Expand Tier I Mouse GO 2710 Genes GS192471: GO:0048869 cellular developmental process
Expand Tier I Mouse MP 577 Genes GS165985: MP:0000965 abnormal sensory neuron morphology
Expand Tier I Human 85 Genes GS173666: HP:0005978 Type II diabetes mellitus
Expand Tier I Mouse MP 623 Genes GS164446: MP:0005195 abnormal posterior eye segment morphology
Expand Tier I Human 202 Genes GS174764: HP:0007367 Atrophy/Degeneration affecting the central nervous system
Expand Tier I Mouse MP 482 Genes GS167105: MP:0008948 decreased neuron number
Expand Tier I Human GO 4085 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Mouse MP 209 Genes GS165114: MP:0004426 abnormal cochlear labyrinth morphology
Expand Tier I Human 136 Genes GS171855: HP:0000597 Ophthalmoparesis
Expand Tier I Mouse MP 3522 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier I Mouse MP 48 Genes GS169803: MP:0003730 abnormal photoreceptor inner segment morphology
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human 356 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Human 471 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Human 164 Genes GS174994: HP:0002059 Cerebral atrophy
Expand Tier I Human GO 39 Genes GS202686: GO:0060113 inner ear receptor cell differentiation
Expand Tier I Mouse GO 8386 Genes GS189751: GO:0050794 regulation of cellular process
Expand Tier I Mouse 455 Genes GS136697: systematic lupus erythematosus susceptibility 1a (Sle1a, Published QTL Chr 1)
Expand Tier I Mouse MP 52 Genes GS167572: MP:0001006 abnormal retinal cone cell morphology
Expand Tier I Mouse GO 24 Genes GS186963: GO:0045494 photoreceptor cell maintenance
Expand Tier II Mouse 303 Genes GS84117: alcohol withdrawal (Published QTL, Chr 1)
Expand Tier I Mouse 385 Genes GS135459: bone mineral density 5 (Bomd5, Published QTL Chr 1)
Expand Tier I Mouse 330 Genes GS136796: total body bone mineral density 1 (Tbbmd1, Published QTL Chr 1)
Expand Tier I Mouse MP 106 Genes GS166716: MP:0003729 abnormal photoreceptor outer segment morphology
Expand Tier I Mouse GO 49 Genes GS185850: GO:0060113 inner ear receptor cell differentiation
Expand Tier I Human GO 185 Genes GS196034: GO:0031253 cell projection membrane
Expand Tier I Mouse 465 Genes GS135539: cerebellum weight 1 (Cbm1, Published QTL Chr 1)
Expand Tier I Human 550 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Mouse GO 26 Genes GS181543: GO:0001917 photoreceptor inner segment
Expand Tier I Human 361 Genes GS173991: HP:0000505 Visual impairment
Expand Tier II Mouse 124 Genes GS84120: high-dose ethanol actions (Published QTL, Chr 1)
Expand Tier I Human GO 45 Genes GS205662: GO:0042490 mechanoreceptor differentiation
Expand Tier I Mouse MP 1415 Genes GS169531: MP:0005391 vision/eye phenotype
Expand Tier I Mouse 385 Genes GS136441: peak bone mineral density 1 (Pbmd1, Published QTL Chr 1)
Expand Tier I Mouse 465 Genes GS136563: radiation pulmonary fibrosis 2 (Radpf2, Published QTL Chr 1)
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 1068 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 695 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Mouse GO 8942 Genes GS185492: GO:0050789 regulation of biological process
Expand Tier I Human GO 4 Genes GS199423: GO:0002142 stereocilia ankle link complex
Expand Tier I Mouse 465 Genes GS135805: emotionality 1 (Emo1, Published QTL Chr 1)
Expand Tier I Mouse MP 204 Genes GS165391: MP:0000972 abnormal mechanoreceptor morphology
Expand Tier I Human 541 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier II Mouse 93 Genes GS34767: Whole Brain Gene expression correlates of Novel environment vertical activity counts minutes 45-60 in Females & Males BXD
Expand Tier I Human 469 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Mouse GO 10879 Genes GS181473: GO:0005488 binding
Expand Human 14 Genes GS221900: Capture panel of retinitis pigmentosa (RP) genes used to diagnose Italian probands
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 GO 5892 Genes GS180036: GO:0032501 multicellular organismal process
Expand Tier I Mouse GO 825 Genes GS187237: GO:0030182 neuron differentiation
Expand Tier I Mouse 467 Genes GS136343: natural killer T cell numbers 1 (Nktcn1, Published QTL Chr 1)
Expand Tier I Mouse 449 Genes GS136475: plasma cholesterol 1 (Pcho1, Published QTL Chr 1)
Expand Tier I Human GO 8578 Genes GS196930: GO:0065007 biological regulation
Expand Tier II Mouse 435 Genes GS84108: cocaine related behavior Chr1 at D1Ncvs12 (Published QTL)
Expand Tier I Mouse GO 8145 Genes GS190714: GO:0016020 membrane
Expand Tier I Mouse 465 Genes GS136269: modifier of Notch (Mnotch, Published QTL Chr 1)
Expand Tier I Mouse MP 569 Genes GS165809: MP:0002864 abnormal ocular fundus morphology
Expand Tier I Mouse 434 Genes GS135508: body weight at 8 weeks QTL 1 (Bw8q1, Published QTL Chr 1)
Expand Tier I Human 220 Genes GS171139: HP:0005288 Abnormality of the nares
Expand Tier I Human GO 7717 Genes GS207616: GO:0016020 membrane
Expand Tier I Human GO 68 Genes GS204815: GO:0005902 microvillus
Expand Tier I Mouse GO 1394 Genes GS191552: GO:0042995 cell projection
Expand Tier I Human 78 Genes GS173104: HP:0000670 Carious teeth
Expand Tier I Mouse 465 Genes GS135601: circulating hormone level QTL 1 (Chlq1, Published QTL Chr 1)
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Human 54 Genes GS221925: Capture panel of retinitis pigmentosa (RP) genes used to diagnose Irish probands
Expand Tier I Mouse GO 3614 Genes GS180229: GO:0005886 plasma membrane
Expand Tier I Mouse GO 4333 Genes GS184452: GO:0044422 organelle part
Expand Tier I Human GO 1722 Genes GS198004: GO:0007399 nervous system development
Expand Tier I Human GO 27 Genes GS198431: GO:0032421 stereocilium bundle
Expand Tier I Human 148 Genes GS172295: HP:0001513 Obesity
Expand Tier I Mouse GO 4073 Genes GS180034: GO:0032502 developmental process
Expand Tier I Human GO 4201 Genes GS195112: GO:0071840 cellular component organization or biogenesis
Expand Tier I Mouse GO 444 Genes GS189435: GO:0044297 cell body
Expand Tier I Mouse 465 Genes GS136751: susceptibility to Salmonella typhimurium antigens 2 (Ssta2, Published QTL Chr 1)
Expand Tier I Mouse 465 Genes GS136863: triglycerides (Trglyd, Published QTL Chr 1)
Expand Tier I Human GO 3098 Genes GS203058: GO:0048519 negative regulation of biological process
Expand Tier II Mouse 443 Genes GS84110: Acute ethanol sensitivity on Chr1 (Published QTL)
Expand Tier I Human 95 Genes GS176989: HP:0008047 Abnormality of the vasculature of the eye
Expand Tier I Mouse GO 609 Genes GS185024: GO:0044463 cell projection part
Expand Tier I Human GO 3506 Genes GS193991: GO:0048731 system development
Expand Tier I Human 381 Genes GS175714: HP:0011389 Functional abnormality of the inner ear
Expand Tier I Mouse MP 247 Genes GS163316: MP:0000035 abnormal membranous labyrinth morphology
Expand Tier I Mouse 465 Genes GS136257: melanoma modifier 2 (Melm2, Published QTL Chr 1)
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 Mouse 465 Genes GS135677: cholesterol QTL 6 (Cq6, Published QTL Chr 1)
Expand Tier I Mouse GO 1041 Genes GS184451: GO:0044421 extracellular region part
Expand Tier I Human 187 Genes GS171512: HP:0007703 Abnormal retinal pigmentation
Expand Tier I Mouse 377 Genes GS136613: colon tumor susceptibility 3 (Scc3, Published QTL Chr 1)
Expand Tier I Mouse MP 487 Genes GS166123: MP:0002102 abnormal ear morphology
Expand Tier I Human 413 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Mouse GO 6947 Genes GS192918: GO:0050896 response to stimulus
Expand Tier I Mouse GO 1825 Genes GS193270: GO:0005576 extracellular region
Expand Tier I Mouse GO 2138 Genes GS186067: GO:0050877 neurological system process
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 182 Genes GS176955: HP:0000431 Wide nasal bridge
Expand Tier I Human GO 4 Genes GS199415: GO:0002141 stereocilia ankle link
Expand Tier I Mouse MP 16 Genes GS167659: MP:0008444 retinal cone cell degeneration
Expand Tier I Human 368 Genes GS170971: HP:0000407 Sensorineural hearing impairment
Expand Tier I Human 442 Genes GS175423: HP:0010461 Abnormality of the male genitalia
Expand Tier II Mouse 376 Genes GS35779: Neocortex Gene expression correlates of CPP - Time (s) in drug-paired compartment a in Males BXD
Expand Tier I Mouse MP 459 Genes GS163138: MP:0005253 abnormal eye physiology
Expand Tier I Mouse 460 Genes GS136103: lupus NZB x NZW 7 (Lbw7, Published QTL Chr 1)
Expand Tier I Mouse GO 2498 Genes GS193018: GO:0003008 system process
Expand Tier I Mouse MP 207 Genes GS167140: MP:0003169 abnormal scala media morphology
Expand Tier II Mouse 435 Genes GS84109: METH responses for climbing on Chr1 at D1Ncvs12 (Published QTL)
Expand Tier I Mouse MP 71 Genes GS165854: MP:0004406 abnormal cochlear hair cell number
Expand Tier I Human 120 Genes GS171657: HP:0000613 Photophobia
Expand Tier I Human GO 636 Genes GS201839: GO:0044463 cell projection part
Expand Tier III Mouse 8331 Genes GS128199: Alcohol Preference union of 86 Gene Sets
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Human 308 Genes GS172100: HP:0000587 Abnormality of the optic nerve
Expand Tier I Human GO 1135 Genes GS205691: GO:0022008 neurogenesis
Expand Tier II Mouse 411 Genes GS84107: ethanol conditioned taste aversion on Chr1 (Published QTL)
Expand Tier I Human 316 Genes GS175597: HP:0011013 Abnormality of carbohydrate metabolism/homeostasis
Expand Tier I Human 382 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Human GO 6548 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human 513 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Mouse GO 18 Genes GS181644: GO:0032420 stereocilium
Expand Human 74 Genes GS221014: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PEROXISOME
Expand Tier I Mouse 465 Genes GS136467: pentobarbital withdrawal modifier (Pbwm, Published QTL Chr 1)
Expand Tier I Mouse 467 Genes GS136729: susceptibility to lung cancer 5 (Sluc5, Published QTL Chr 1)
Expand Tier I Human GO 51 Genes GS201433: GO:0005518 collagen binding
Expand Tier I Mouse GO 2991 Genes GS182469: GO:0043234 protein complex
Expand Human 74 Genes GS219653: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PEROXISOME
Expand Tier II Mouse 137 Genes GS84119: alcohol consumption (Published QTL, Chr 1)
Expand Tier I Mouse MP 51 Genes GS168880: MP:0004736 abnormal distortion product otoacoustic emission
Expand Tier I Mouse 465 Genes GS135916: graft-versus-host disease 1 (Gvhd1, Published QTL Chr 1)
Expand Tier III Human 102 Genes GS14904: Genes Harboring Allelic Variants That Distinguish Successful vs Unsuccessful Nicotine Abstainers in at Least 2 Samples
Expand Tier III Rat 555 Genes GS223271: Bone structure and strength QTL 34 (Bss34 Published QTL Chr 13)
Expand Tier I Human GO 2539 Genes GS203335: GO:0048513 organ development
Expand Tier I Mouse GO 55 Genes GS188801: GO:0042490 mechanoreceptor differentiation
Expand Tier I Human 199 Genes GS176660: HP:0000050 Hypoplastic genitalia
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 I Human 381 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Human 917 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Mouse GO 41 Genes GS184631: GO:0005518 collagen binding
Expand Tier I Mouse MP 223 Genes GS169032: MP:0005551 abnormal eye electrophysiology
Expand Tier I Human 604 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human 88 Genes GS173329: HP:0000682 Abnormality of dental enamel
Expand Tier I Human GO 431 Genes GS196987: GO:0045596 negative regulation of cell differentiation
Expand Tier I Mouse 465 Genes GS135234: activity response to ethanol 1 (Actre1, Published QTL Chr 1)
Expand Tier I Mouse GO 1463 Genes GS189746: GO:0050793 regulation of developmental process
Expand Tier I Human 985 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Mouse GO 3583 Genes GS180236: GO:0032991 macromolecular complex
Expand Tier I Mouse 460 Genes GS135935: HDL level 34 (Hdl34, Published QTL Chr 1)
Expand Tier I Human GO 29 Genes GS198369: GO:0017022 myosin binding
Expand Tier I Mouse 467 Genes GS136594: rotarod performance 1 (Rrodp1, Published QTL Chr 1)
Expand Tier I Mouse GO 65 Genes GS187955: GO:0005902 microvillus
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Mouse GO 102 Genes GS178598: GO:0072372 primary cilium
Expand Tier I Human GO 6073 Genes GS201252: GO:0044425 membrane part
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 Mouse 369 Genes GS84114: activity response to ethanol (Published QTL, Chr 1)
Expand Tier I Human GO 1223 Genes GS208482: GO:0042995 cell projection
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 465 Genes GS135867: fasting glucose 2 (Fglu2, Published QTL Chr 1)
Expand Tier I Human 511 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human GO 7650 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier I Human GO 205 Genes GS209987: GO:0050953 sensory perception of light stimulus
Expand Tier I Human GO 294 Genes GS209721: GO:0045177 apical part of cell
Expand Human 492 Genes GS222864: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_METABOLISM_OF_LIPIDS_AND_LIPOPROTEINS
Expand Tier I Mouse 460 Genes GS136692: systemic lupus erythmatosus susceptibility 1 (Sle1, Published QTL Chr 1)
Expand Tier I Mouse GO 133 Genes GS193043: GO:0050954 sensory perception of mechanical stimulus
Expand Tier I Mouse 906 Genes GS129103: bone mineral density 5 (Bmd5 Published QTL Chr 1)
Expand Tier I Mouse 454 Genes GS136740: spermatocyte heat stress resistance 1 (Sphsr1, Published QTL Chr 1)
Expand Tier I Human GO 1435 Genes GS205623: GO:0009888 tissue development
Expand Tier I Mouse 465 Genes GS135673: cholesterol QTL 2 (Cq2, Published QTL Chr 1)
Expand Tier I Human 42 Genes GS174449: HP:0001123 Visual field defect
Expand Tier I Human 220 Genes GS171791: HP:0000370 Abnormality of the middle ear
Expand Tier I Human 411 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Mouse 454 Genes GS136381: obesity QTL 9 (Obq9, Published QTL Chr 1)
Expand Tier I Mouse 460 Genes GS135583: chronic glomerulonephritis in NZM 1 (Cgnz1, Published QTL Chr 1)
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 1222 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Mouse GO 553 Genes GS188475: GO:0051093 negative regulation of developmental process
Expand Tier I Mouse GO 28 Genes GS181643: GO:0032421 stereocilium bundle
Expand Tier I Human GO 5359 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier III Rat 922 Genes GS223612: Blood pressure QTL 244 (Bp244 Published QTL Chr 13)
Expand Tier I Human GO 1066 Genes GS196002: GO:0048699 generation of neurons
Expand Tier I Human 90 Genes GS170889: HP:0006482 Abnormality of dental morphology
Expand Tier I Mouse GO 213 Genes GS193348: GO:0016324 apical plasma membrane
Expand Tier I Human GO 3853 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Human GO 90 Genes GS208328: GO:0005604 basement membrane
Expand Tier I Mouse GO 94 Genes GS191405: GO:0005604 basement membrane
Expand Tier I Human 288 Genes GS175335: HP:0000036 Abnormality of the penis
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 I Mouse MP 142 Genes GS169847: MP:0004399 abnormal cochlear outer hair cell morphology
Expand Tier I Mouse GO 37 Genes GS181873: GO:0043954 cellular component maintenance
Expand Tier I Mouse MP 702 Genes GS167922: MP:0000959 abnormal somatic sensory system morphology
Expand Tier I Mouse GO 23 Genes GS187859: GO:0032391 photoreceptor connecting cilium
Expand Tier I Human GO 132 Genes GS209984: GO:0050954 sensory perception of mechanical stimulus
Expand Tier I Mouse MP 433 Genes GS165390: MP:0003224 neuron degeneration
Expand Tier I Human CTD 1151 Genes GS121437: Fluorouracil interacting genes (MeSH:D005472) in CTD
Expand Tier I Human 209 Genes GS173206: HP:0003241 Genital hypoplasia
Expand Tier I Human 157 Genes GS171968: HP:0000405 Conductive hearing impairment
Expand Tier I Human GO 23 Genes GS198432: GO:0032420 stereocilium
Expand Tier I Mouse 466 Genes GS135476: bone response to mechanical loading 1 (Brml1, Published QTL Chr 1)
Expand Tier I Mouse 458 Genes GS136698: systematic lupus erythematosus susceptibility 1b (Sle1b, Published QTL Chr 1)
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
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 158 Genes GS171900: HP:0011452 Functional abnormality of the middle ear
Expand Tier I Mouse 465 Genes GS135501: basal locomotor activity 4 (Bslm4, Published QTL Chr 1)
Expand Tier III Rat 381 Genes GS223355: Glomerulus QTL 15 (Glom15 Published QTL Chr 13)
Expand Tier I Mouse MP 11449 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Mouse GO 141 Genes GS179265: GO:0031253 cell projection membrane
Expand Tier I Mouse GO 2538 Genes GS190893: GO:0030154 cell differentiation
Expand Tier I Mouse 467 Genes GS135683: Ctla4 expression QTL (Ctex, Published QTL Chr 1)
Expand Tier I Human GO 4250 Genes GS197009: GO:0005886 plasma membrane
Expand Tier I Human 50 Genes GS173561: HP:0000691 Microdontia
Expand Tier I Human 496 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Human GO 6347 Genes GS201256: GO:0044422 organelle part
Expand Tier II Mouse 151 Genes GS34251: Striatum Gene expression correlates of Activity in altered context during presentation of cue in Males BXD
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 104 Genes GS129202: zinc induced tolerance 1 (Zit1 Published QTL Chr 1)
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 413 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Human 62 Genes GS221933: Mutations of 60 known causative genes in 157 families with retinitis pigmentosa (RP) based on exome sequencing
Expand Tier I Human GO 2816 Genes GS209411: GO:0048869 cellular developmental process
Expand Tier III Rat 538 Genes GS223607: Blood pressure QTL 241 (Bp241 Published QTL Chr 13)
Expand Tier I Human 284 Genes GS175594: HP:0011014 Abnormal glucose homeostasis
Expand Tier I Mouse GO 5879 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Mouse GO 4 Genes GS182628: GO:0002142 stereocilia ankle link complex
Expand Tier I Human GO 425 Genes GS196302: GO:0031012 extracellular matrix
Expand Tier II Mouse 324 Genes GS84116: ethanol withdrawal on Chr1 at Xmv41 (Published QTL)
Expand Tier I Mouse GO 3605 Genes GS190682: GO:0007275 multicellular organismal development
Expand Tier I Human 886 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 209 Genes GS175990: HP:0000463 Anteverted nares
Expand Tier I Human GO 3271 Genes GS199267: GO:0043234 protein complex
Expand Tier II Mouse 85 Genes GS34574: Striatum Gene expression correlates of Novel environment distance (cm) travelled minutes 0-15 in Males BXD
Expand Tier III Rat 894 Genes GS223393: Experimental allergic encephalomyelitis QTL 17 (Eae17 Published QTL Chr 13)
Expand Tier II Mouse 187 Genes GS84118: ethanol induced locomotion (Published QTL, Chr 1)
Expand Tier I Mouse 465 Genes GS135799: escape latencies during navigation task (Elnt, Published QTL Chr 1)
Expand Tier I Mouse 430 Genes GS135968: HDL QTL 5 (Hdlq5, Published QTL Chr 1)
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 Mouse 385 Genes GS135969: HDL QTL 6 (Hdlq6, Published QTL Chr 1)
Expand Tier I Mouse GO 4 Genes GS182620: GO:0002141 stereocilia ankle link
Expand Tier I Human GO 1094 Genes GS201255: GO:0044421 extracellular region part
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Mouse 467 Genes GS136771: SWR lupus locus 1 (Swrl1, Published QTL Chr 1)
Expand Tier I Mouse GO 1038 Genes GS180208: GO:0045595 regulation of cell differentiation
Expand Tier I Mouse 465 Genes GS135290: alcohol withdrawal 1 (Alcw1, Published QTL Chr 1)
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 I Mouse 460 Genes GS135578: cystic fibrosis modifier QTL 1 (Cfmq1, Published QTL Chr 1)
Expand Tier I Human GO 3116 Genes GS199272: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier I Human 837 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 273 Genes GS172516: HP:0001347 Hyperreflexia
Expand Tier I Mouse GO 1550 Genes GS192290: GO:0007600 sensory perception
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Mouse GO 6204 Genes GS184629: GO:0005515 protein binding
Expand Tier I Human 78 Genes GS172553: HP:0100689 Decreased corneal thickness
Expand Tier I Mouse MP 179 Genes GS163498: MP:0003308 abnormal cochlear sensory epithelium morphology
Expand Tier I Mouse MP 1327 Genes GS163971: MP:0002092 abnormal eye morphology
Expand Tier I Mouse MP 542 Genes GS165385: MP:0008946 abnormal neuron number
Expand Tier I Human 77 Genes GS173703: HP:0000842 Hyperinsulinemia
Expand Tier I Mouse 346 Genes GS129094: bone mineral density 1 (Bmd1 Published QTL Chr 1)
Expand Tier I Mouse GO 9323 Genes GS180152: GO:0065007 biological regulation
Expand Tier III Rat 795 Genes GS224055: Renal function QTL 47 (Rf47 Published QTL Chr 13)