Gene Details



CRX and homologs in 1 species are found in 249 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 385 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Human GO 1050 Genes GS202082: GO:0051254 positive regulation of RNA metabolic process
Expand Tier I Human GO 14 Genes GS200472: GO:0030275 LRR domain binding
Expand Tier I Human 877 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human GO 3714 Genes GS194038: GO:1901362 organic cyclic compound biosynthetic process
Expand Tier I Human GO 3108 Genes GS198685: GO:0048522 positive regulation of cellular process
Expand Tier I Human 64 Genes GS174379: HP:0002084 Encephalocele
Expand Tier I Human GO 7609 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier III Human 49 Genes GS221924: Capture panel of retinitis pigmentosa (RP) genes used to diagnose Chinese probands
Expand Tier I Human 231 Genes GS176771: HP:0001000 Abnormality of skin pigmentation
Expand Tier I Human GO 5184 Genes GS208954: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Human 829 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 42 Genes GS174449: HP:0001123 Visual field defect
Expand Tier I Human 81 Genes GS171773: HP:0000532 Chorioretinal abnormality
Expand Tier I Human 220 Genes GS171791: HP:0000370 Abnormality of the middle ear
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 92 Genes GS171656: HP:0000610 Abnormality of the choroid
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 177 Genes GS171047: HP:0008736 Hypoplasia of penis
Expand Tier I Human 535 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Tier I Human 274 Genes GS172372: HP:0000648 Optic atrophy
Expand Tier I Human 1222 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human GO 9526 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human GO 1278 Genes GS201265: GO:0009891 positive regulation of biosynthetic process
Expand Tier I Human GO 1171 Genes GS203018: GO:0045935 positive regulation of nucleobase-containing compound metabolic process
Expand Tier I Human GO 9155 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human GO 3304 Genes GS210180: GO:0031326 regulation of cellular biosynthetic process
Expand Tier I Human 169 Genes GS173988: HP:0000501 Glaucoma
Expand Tier I Human GO 3099 Genes GS206544: GO:2000112 regulation of cellular macromolecule biosynthetic process
Expand Tier I Human GO 1255 Genes GS210178: GO:0031328 positive regulation of cellular biosynthetic process
Expand Tier I Human 248 Genes GS176844: HP:0000429 Abnormality of the nasal alae
Expand Tier I Human GO 6256 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human GO 276 Genes GS206897: GO:0001654 eye development
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
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 280 Genes GS176231: HP:0010938 Abnormality of the external nose
Expand Tier I Human GO 1214 Genes GS198360: GO:0006357 regulation of transcription from RNA polymerase II promoter
Expand Tier I Human GO 2047 Genes GS203406: GO:0009653 anatomical structure morphogenesis
Expand Tier I Human GO 3334 Genes GS205622: GO:0009889 regulation of biosynthetic process
Expand Tier I Human 100 Genes GS176744: HP:0000987 Atypical scarring of skin
Expand Tier I Human 89 Genes GS176988: HP:0008046 Abnormality of the retinal vasculature
Expand Tier I Human GO 1079 Genes GS209282: GO:0010628 positive regulation of gene expression
Expand Tier I Human GO 3853 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human 288 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier I Human GO 5400 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Human GO 1197 Genes GS199501: GO:0051173 positive regulation of nitrogen compound metabolic process
Expand Tier I Human 1002 Genes GS174914: HP:0003011 Abnormality of the musculature
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 486 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human 201 Genes GS171631: HP:0008051 Abnormality of the retinal pigment epithelium
Expand Tier I Human GO 4129 Genes GS206329: GO:0060255 regulation of macromolecule metabolic process
Expand Tier I Human 171 Genes GS173019: HP:0000819 Diabetes mellitus
Expand Tier I Human GO 5348 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Human GO 3180 Genes GS208061: GO:0010556 regulation of macromolecule biosynthetic process
Expand Tier I Human GO 5908 Genes GS195199: GO:0005634 nucleus
Expand Tier I Human 85 Genes GS173666: HP:0005978 Type II diabetes mellitus
Expand Tier I Human 136 Genes GS171855: HP:0000597 Ophthalmoparesis
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human GO 8 Genes GS197112: GO:0043522 leucine zipper domain binding
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 290 Genes GS198991: GO:0005667 transcription factor complex
Expand Tier I Human 122 Genes GS171946: HP:0002269 Abnormality of neuronal migration
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 471 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Human GO 4415 Genes GS203072: GO:0090304 nucleic acid metabolic process
Expand Tier I Human 120 Genes GS172358: HP:0003117 Abnormality of circulating hormone level
Expand Tier I Human 209 Genes GS173206: HP:0003241 Genital hypoplasia
Expand Tier I Human GO 2711 Genes GS199273: GO:0043233 organelle lumen
Expand Tier I Human 157 Genes GS171968: HP:0000405 Conductive hearing impairment
Expand Tier I Human 156 Genes GS172363: HP:0004324 Increased body weight
Expand Tier I Human 936 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human 598 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
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 GO 999 Genes GS195678: GO:0003700 sequence-specific DNA binding transcription factor activity
Expand Tier I Human 550 Genes GS171251: HP:0003549 Abnormality of connective tissue
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 Human 361 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human 782 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human CTD 6287 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human GO 539 Genes GS199393: GO:0019904 protein domain specific binding
Expand Tier I Human 636 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human GO 1476 Genes GS203369: GO:0005654 nucleoplasm
Expand Tier I Human 496 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
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 Human GO 6347 Genes GS201256: GO:0044422 organelle part
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 Human GO 792 Genes GS205616: GO:0009887 organ morphogenesis
Expand Tier I Human GO 5190 Genes GS207857: GO:0009058 biosynthetic process
Expand Tier I Human GO 2665 Genes GS205543: GO:0070013 intracellular organelle lumen
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 Human 423 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Human GO 4354 Genes GS210182: GO:0031323 regulation of cellular metabolic process
Expand Tier I Human GO 8578 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human GO 3383 Genes GS200312: GO:0019219 regulation of nucleobase-containing compound metabolic process
Expand Tier I Human GO 7308 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 323 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 220 Genes GS171139: HP:0005288 Abnormality of the nares
Expand Tier I Human GO 8948 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human GO 2878 Genes GS206108: GO:2001141 regulation of RNA biosynthetic process
Expand Tier I Human 413 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier I Human 614 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Human 62 Genes GS221933: Mutations of 60 known causative genes in 157 families with retinitis pigmentosa (RP) based on exome sequencing
Expand Human 54 Genes GS221925: Capture panel of retinitis pigmentosa (RP) genes used to diagnose Irish probands
Expand Tier I Human 8 Genes GS171975: HP:0000533 Chorioretinal atrophy
Expand Tier I Human GO 3178 Genes GS204204: GO:0006351 transcription, DNA-dependent
Expand Tier I Human 148 Genes GS172295: HP:0001513 Obesity
Expand Tier I Human 284 Genes GS175594: HP:0011014 Abnormal glucose homeostasis
Expand Tier I Human GO 6605 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 1218 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 I Human 532 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Human 195 Genes GS222320: Genes associated with high risk of intellectual disability.
Expand Tier I Human 886 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human GO 688 Genes GS194602: GO:0045944 positive regulation of transcription from RNA polymerase II promoter
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 Human 45 Genes GS174869: HP:0000551 Abnormality of color vision
Expand Tier I Human 209 Genes GS175990: HP:0000463 Anteverted nares
Expand Tier I Human GO 4292 Genes GS204746: GO:0080090 regulation of primary metabolic process
Expand Tier I Human GO 3271 Genes GS199267: GO:0043234 protein complex
Expand Tier I Human GO 2479 Genes GS201249: GO:0044428 nuclear part
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 4138 Genes GS207925: GO:0034645 cellular macromolecule biosynthetic process
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human GO 5347 Genes GS203642: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Human 95 Genes GS176989: HP:0008047 Abnormality of the vasculature of the eye
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 3603 Genes GS198456: GO:0019438 aromatic compound biosynthetic process
Expand Tier I Human GO 3891 Genes GS203908: GO:0016070 RNA metabolic process
Expand Tier I Human GO 5567 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Human GO 1876 Genes GS210181: GO:0031325 positive regulation of cellular metabolic process
Expand Tier I Human GO 204 Genes GS210485: GO:0007601 visual perception
Expand Tier I Human GO 4787 Genes GS204612: GO:0019222 regulation of metabolic process
Expand Tier I Human 95 Genes GS176616: HP:0000662 Night blindness
Expand Tier I Human GO 106 Genes GS204694: GO:0060041 retina development in camera-type eye
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 2939 Genes GS202080: GO:0051252 regulation of RNA metabolic process
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 5526 Genes GS194040: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Human GO 3277 Genes GS194088: GO:0003676 nucleic acid binding
Expand Tier I Human 413 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Human 389 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
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 1977 Genes GS204568: GO:0009893 positive regulation of metabolic process
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 I Human 140 Genes GS174860: HP:0010549 Paralysis due to lesions of the principle motor tracts
Expand Tier I Human GO 2092 Genes GS209551: GO:0031981 nuclear lumen
Expand Tier I Human GO 3264 Genes GS205266: GO:0032774 RNA biosynthetic process
Expand Tier I Human GO 2756 Genes GS194555: GO:0031974 membrane-enclosed lumen
Expand Tier I Human 120 Genes GS171657: HP:0000613 Photophobia
Expand Tier I Human 837 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 908 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Human 273 Genes GS172516: HP:0001347 Hyperreflexia
Expand Tier I Human 342 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human 64 Genes GS172899: HP:0011815 Cephalocele
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Human 70 Genes GS222261: Genes associated with retinitis pigmentosa (RP) on OMIM database
Expand Tier I Human 308 Genes GS172100: HP:0000587 Abnormality of the optic nerve
Expand Tier I Human GO 5928 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human GO 7259 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human GO 818 Genes GS197472: GO:0044451 nucleoplasm part
Expand Tier I Human GO 5014 Genes GS210357: GO:0044249 cellular biosynthetic process
Expand Tier I Human 316 Genes GS175597: HP:0011013 Abnormality of carbohydrate metabolism/homeostasis
Expand Tier I Human GO 493 Genes GS209225: GO:0007600 sensory perception
Expand Tier I Human 382 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Human 203 Genes GS174706: HP:0000553 Abnormality of the uvea
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 Human 78 Genes GS172553: HP:0100689 Decreased corneal thickness
Expand Human 70 Genes GS221898: RetNet genes linked to retinitis pigmentosa (RP)
Expand Tier I Human GO 237 Genes GS203525: GO:0043010 camera-type eye development
Expand Tier I Human GO 3550 Genes GS203607: GO:0034654 nucleobase-containing compound biosynthetic process
Expand Tier I Human GO 3617 Genes GS206953: GO:0018130 heterocycle biosynthetic process
Expand Tier I Human GO 3468 Genes GS199499: GO:0051171 regulation of nitrogen compound metabolic process
Expand Tier I Human GO 3432 Genes GS203057: GO:0048518 positive regulation of biological process
Expand Tier I Human GO 2539 Genes GS203335: GO:0048513 organ development
Expand Tier I Human 199 Genes GS176660: HP:0000050 Hypoplastic genitalia
Expand Tier I Human GO 3697 Genes GS194499: GO:0044271 cellular nitrogen compound biosynthetic process
Expand Tier I Human CTD 5732 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
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 381 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Human 77 Genes GS173703: HP:0000842 Hyperinsulinemia
Expand Tier I Human 917 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 65 Genes GS171651: HP:0000618 Blindness
Expand Tier I Human GO 676 Genes GS196540: GO:0043565 sequence-specific DNA binding
Expand Tier I Human GO 8645 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 985 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Human 103 Genes GS173741: HP:0100699 Scarring
Expand Tier I Human 97 Genes GS173091: HP:0004374 Hemiplegia/hemiparesis
Expand Tier I Human GO 1001 Genes GS204232: GO:0001071 nucleic acid binding transcription factor activity
Expand Tier I Human GO 4245 Genes GS207858: GO:0009059 macromolecule biosynthetic process
Expand Tier I Human 397 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human GO 2857 Genes GS195291: GO:0006355 regulation of transcription, DNA-dependent
Expand Tier I Human GO 5337 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier I Human GO 3325 Genes GS205369: GO:0010468 regulation of gene expression
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 79 Genes GS175373: HP:0011486 Abnormality of corneal thickness
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 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 GO 1179 Genes GS208060: GO:0010557 positive regulation of macromolecule biosynthetic process
Expand Tier I Human GO 205 Genes GS209987: GO:0050953 sensory perception of light stimulus
Expand Tier I Human 3 Genes GS175610: HP:0007994 Peripheral visual field loss
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 Human GO 4554 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human GO 315 Genes GS204842: GO:0003682 chromatin binding
Expand Tier I Human 124 Genes GS175492: HP:0000512 Abnormal electroretinogram
Expand Tier I Human GO 1391 Genes GS193937: GO:0006366 transcription from RNA polymerase II promoter
Expand Tier I Human GO 10576 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 4682 Genes GS205364: GO:0010467 gene expression
Expand Tier I Human 532 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Human 24 Genes GS221927: Targeted exome capture and sequencing identifies novel PRPF31 mutations in autosomal dominant retinitis pigmentosa (RP) in Chinese families
Expand Tier I Human 36 Genes GS174701: HP:0000556 Retinal dystrophy
Expand Tier I Human 1203 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human GO 2310 Genes GS195643: GO:0003677 DNA binding
Expand Tier I Human 5 Genes GS176096: HP:0000548 Cone-rod dystrophy
Expand Tier I Human GO 1839 Genes GS198572: GO:0010604 positive regulation of macromolecule metabolic process
Expand Tier I Human GO 5120 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Tier I Human GO 999 Genes GS195340: GO:0045893 positive regulation of transcription, DNA-dependent
Expand Tier I Human GO 5623 Genes GS196808: GO:0032501 multicellular organismal process