Gene Details



RS1 and homologs in 1 species are found in 127 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 4567 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human 124 Genes GS175492: HP:0000512 Abnormal electroretinogram
Expand Tier I Human GO 1319 Genes GS208126: GO:0009605 response to external stimulus
Expand Tier I Human GO 2139 Genes GS210214: GO:0005576 extracellular region
Expand Tier I Human GO 146 Genes GS208908: GO:0071214 cellular response to abiotic stimulus
Expand Tier I Human 3 Genes GS170855: HP:0001105 Retinal atrophy
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human GO 47 Genes GS200701: GO:0009583 detection of light stimulus
Expand Tier I Human GO 36 Genes GS202157: GO:0003407 neural retina development
Expand Tier I Human 37 Genes GS176719: HP:0000541 Retinal detachment
Expand Tier I Human GO 90 Genes GS201852: GO:0048593 camera-type eye morphogenesis
Expand Tier I Human GO 68 Genes GS204556: GO:0071478 cellular response to radiation
Expand Tier I Human 81 Genes GS171773: HP:0000532 Chorioretinal abnormality
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human GO 204 Genes GS210485: GO:0007601 visual perception
Expand Tier I Human 414 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human GO 1914 Genes GS198782: GO:0044459 plasma membrane part
Expand Tier I Human GO 1693 Genes GS209960: GO:0003008 system process
Expand Tier I Human 92 Genes GS171656: HP:0000610 Abnormality of the choroid
Expand Tier I Human GO 48 Genes GS199797: GO:0072341 modified amino acid binding
Expand Tier I Human GO 105 Genes GS204694: GO:0060041 retina development in camera-type eye
Expand Tier I Human GO 956 Genes GS200151: GO:0022610 biological adhesion
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 600 Genes GS206615: GO:0007186 G-protein coupled receptor signaling pathway
Expand Tier I Human GO 1097 Genes GS201255: GO:0044421 extracellular region part
Expand Tier I Human 170 Genes GS173988: HP:0000501 Glaucoma
Expand Tier I Human GO 4593 Genes GS206355: GO:0023052 signaling
Expand Tier I Human GO 20 Genes GS197623: GO:0005547 phosphatidylinositol-3,4,5-trisphosphate binding
Expand Tier I Human GO 83 Genes GS200700: GO:0009582 detection of abiotic stimulus
Expand Tier I Human GO 6 Genes GS195768: GO:0010314 phosphatidylinositol-5-phosphate binding
Expand Tier I Human GO 275 Genes GS206897: GO:0001654 eye development
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 15 Genes GS196656: GO:0001786 phosphatidylserine binding
Expand Tier I Human GO 2 Genes GS200560: GO:0036367 light adaption
Expand Tier I Human 35 Genes GS171655: HP:0000611 Choroid coloboma
Expand Tier I Human GO 8137 Genes GS202316: GO:0050789 regulation of biological process
Expand Tier I Human GO 4084 Genes GS209199: GO:0007165 signal transduction
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human CTD 239 Genes GS122047: Ethylnitrosourea interacting genes (MeSH:D005038) in CTD
Expand Tier I Human 166 Genes GS171901: HP:0010985 Gonosomal inheritance
Expand Tier I Human GO 2050 Genes GS203406: GO:0009653 anatomical structure morphogenesis
Expand Tier I Human GO 4719 Genes GS195977: GO:0007154 cell communication
Expand Tier I Human 1 Genes GS175000: HP:0007667 Cystic retinal degeneration
Expand Tier I Human 1 Genes GS175853: HP:0007984 Reduced amplitude of b-wave (ERG)
Expand Tier I Human 47 Genes GS171072: HP:0000572 Visual loss
Expand Tier I Human GO 124 Genes GS194482: GO:0019898 extrinsic to membrane
Expand Tier I Human GO 494 Genes GS197619: GO:0005543 phospholipid binding
Expand Tier I Human GO 4371 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Human GO 2392 Genes GS206737: GO:0043168 anion binding
Expand Tier I Human 344 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 738 Genes GS208665: GO:0008289 lipid binding
Expand Tier I Human GO 495 Genes GS209225: GO:0007600 sensory perception
Expand Tier I Human 4 Genes GS173799: HP:0001150 Choroidal sclerosis
Expand Tier I Human 203 Genes GS174706: HP:0000553 Abnormality of the uvea
Expand Tier I Human GO 29 Genes GS197622: GO:0005546 phosphatidylinositol-4,5-bisphosphate binding
Expand Tier I Human GO 6585 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human 515 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human GO 186 Genes GS200970: GO:0031406 carboxylic acid binding
Expand Tier I Human GO 319 Genes GS207688: GO:0009314 response to radiation
Expand Tier I Human 34 Genes GS174909: HP:0000546 Retinal degeneration
Expand Tier I Human GO 2027 Genes GS206356: GO:0023051 regulation of signaling
Expand Tier I Human GO 236 Genes GS203525: GO:0043010 camera-type eye development
Expand Tier I Human GO 2545 Genes GS203335: GO:0048513 organ development
Expand Tier I Human GO 2317 Genes GS209215: GO:0007166 cell surface receptor signaling pathway
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 435 Genes GS197802: GO:0007423 sensory organ development
Expand Tier I Human GO 5810 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human GO 37 Genes GS210487: GO:0007602 phototransduction
Expand Tier I Human 358 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Human GO 4070 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human 472 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Human GO 1776 Genes GS205147: GO:0009966 regulation of signal transduction
Expand Tier I Human GO 18 Genes GS205342: GO:0032266 phosphatidylinositol-3-phosphate binding
Expand Tier I Human GO 7 Genes GS208725: GO:0070273 phosphatidylinositol-4-phosphate binding
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human GO 1588 Genes GS196772: GO:0048646 anatomical structure formation involved in morphogenesis
Expand Tier I Human GO 11 Genes GS209228: GO:0007603 phototransduction, visible light
Expand Tier I Human 160 Genes GS175806: HP:0001417 X-linked inheritance
Expand Tier I Human GO 4024 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human GO 12 Genes GS196421: GO:0080025 phosphatidylinositol-3,5-bisphosphate binding
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human GO 202 Genes GS209992: GO:0051606 detection of stimulus
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human 364 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human GO 6151 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human GO 13 Genes GS209557: GO:0043325 phosphatidylinositol-3,4-bisphosphate binding
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human GO 2 Genes GS208258: GO:0016062 adaptation of rhodopsin mediated signaling
Expand Tier I Human 34 Genes GS172418: HP:0000567 Chorioretinal coloboma
Expand Tier I Human GO 4283 Genes GS197009: GO:0005886 plasma membrane
Expand Tier I Human GO 39 Genes GS207123: GO:0071482 cellular response to light stimulus
Expand Tier I Human 36 Genes GS172842: HP:0000480 Retinal coloboma
Expand Tier I Human 20 Genes GS174479: HP:0000529 Progressive visual loss
Expand Tier I Human GO 954 Genes GS195976: GO:0007155 cell adhesion
Expand Tier I Human GO 126 Genes GS201851: GO:0048592 eye morphogenesis
Expand Tier I Human 544 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 388 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 1236 Genes GS202899: GO:0050877 neurological system process
Expand Tier I Human GO 806 Genes GS197478: GO:0009628 response to abiotic stimulus
Expand Tier I Human GO 792 Genes GS205616: GO:0009887 organ morphogenesis
Expand Tier I Human GO 7689 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 4593 Genes GS204007: GO:0044700 single organism signaling
Expand Tier I Human 512 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Human GO 102 Genes GS197118: GO:0016597 amino acid binding
Expand Tier I Human GO 854 Genes GS203972: GO:0005615 extracellular space
Expand Tier I Human GO 7 Genes GS207395: GO:0009642 response to light intensity
Expand Tier I Human GO 205 Genes GS209987: GO:0050953 sensory perception of light stimulus
Expand Tier I Human GO 80 Genes GS194476: GO:0019897 extrinsic to plasma membrane
Expand Tier I Human GO 8622 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human GO 22 Genes GS200702: GO:0009584 detection of visible light
Expand Tier I Human GO 37 Genes GS208512: GO:0060042 retina morphogenesis in camera-type eye
Expand Tier I Human GO 17 Genes GS206358: GO:0023058 adaptation of signaling pathway
Expand Tier I Human GO 7808 Genes GS207616: GO:0016020 membrane
Expand Tier I Human GO 203 Genes GS205472: GO:0009416 response to light stimulus
Expand Tier I Human GO 2335 Genes GS206192: GO:0048583 regulation of response to stimulus
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human GO 100 Genes GS200699: GO:0009581 detection of external stimulus
Expand Tier I Human GO 2033 Genes GS201132: GO:0010646 regulation of cell communication
Expand Tier I Human GO 5 Genes GS195141: GO:0016056 rhodopsin mediated signaling pathway
Expand Tier I Human GO 4983 Genes GS199124: GO:0051716 cellular response to stimulus
Expand Tier I Human GO 153 Genes GS203392: GO:0035091 phosphatidylinositol binding
Expand Tier I Human GO 13 Genes GS195191: GO:0010842 retina layer formation
Expand Tier I Human 107 Genes GS172094: HP:0000589 Coloboma
Expand Tier I Human GO 3513 Genes GS193991: GO:0048731 system development