Gene Details



CRX and homologs in 3 species are found in 434 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 7755 Genes GS185131: GO:0044699 single-organism process
Expand Tier I Human 387 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Mouse GO 2982 Genes GS183514: GO:0019219 regulation of nucleobase-containing compound metabolic process
Expand Tier I Mouse MP 11 Genes GS170728: MP:0002565 delayed circadian phase
Expand Tier I Mouse GO 5650 Genes GS183848: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Mouse GO 2855 Genes GS186757: GO:0034654 nucleobase-containing compound biosynthetic process
Expand Tier I Human GO 1050 Genes GS202082: GO:0051254 positive regulation of RNA metabolic process
Expand Tier I Human 882 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Mouse MP 1724 Genes GS164220: MP:0002882 abnormal neuron morphology
Expand Tier I Human GO 3121 Genes GS198685: GO:0048522 positive regulation of cellular process
Expand Tier I Mouse 973 Genes GS136900: ventral midbrain iron content 4 (Vmbic4, Published QTL Chr 7)
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human GO 5216 Genes GS208954: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Human 832 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Mouse GO 1018 Genes GS185261: GO:0051254 positive regulation of RNA metabolic process
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Mouse GO 778 Genes GS186526: GO:0005654 nucleoplasm
Expand Tier I Human 537 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Tier I Human GO 1171 Genes GS203018: GO:0045935 positive regulation of nucleobase-containing compound metabolic process
Expand Tier I Mouse GO 3473 Genes GS190950: GO:0009059 macromolecule biosynthetic process
Expand Tier I Mouse GO 1187 Genes GS181568: GO:0006357 regulation of transcription from RNA polymerase II promoter
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Mouse GO 8630 Genes GS192624: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse GO 8650 Genes GS186743: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse 1024 Genes GS136319: non-HDL QTL 6 (Nhdlq6, Published QTL Chr 7)
Expand Tier I Mouse MP 396 Genes GS170108: MP:0003727 abnormal retinal layer morphology
Expand Tier I Mouse 653 Genes GS135346: Avp transcript abundance QTL 1 (Avptaq1, Published QTL Chr 7)
Expand Tier I Mouse GO 454 Genes GS181012: GO:0007423 sensory organ development
Expand Tier I Mouse MP 146 Genes GS168338: MP:0001502 abnormal circadian rhythm
Expand Tier I Mouse MP 184 Genes GS163581: MP:0001004 abnormal retinal photoreceptor morphology
Expand Tier I Mouse MP 192 Genes GS166394: MP:0003728 abnormal retinal photoreceptor layer morphology
Expand Tier I Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Human GO 5400 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Mouse GO 4887 Genes GS188190: GO:0006807 nitrogen compound metabolic process
Expand Tier I Mouse MP 55 Genes GS165142: MP:0003732 abnormal retinal outer plexiform layer morphology
Expand Tier I Human GO 4070 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human 120 Genes GS172358: HP:0003117 Abnormality of circulating hormone level
Expand Tier I Human GO 2719 Genes GS199273: GO:0043233 organelle lumen
Expand Tier I Human 157 Genes GS172363: HP:0004324 Increased body weight
Expand Tier I Human 602 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Mouse 958 Genes GS136745: spermatogenesis defect 3 (Spmd3, Published QTL Chr 7)
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Mouse GO 4619 Genes GS191019: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Human GO 4024 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human 786 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Mouse GO 3776 Genes GS187887: GO:0080090 regulation of primary metabolic process
Expand Tier I Human 639 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human GO 5223 Genes GS207857: GO:0009058 biosynthetic process
Expand Tier I Mouse MP 648 Genes GS168389: MP:0001186 pigmentation phenotype
Expand Tier I Human 426 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Mouse MP 3019 Genes GS165466: MP:0003632 abnormal nervous system morphology
Expand Tier I Human 324 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier I Mouse GO 2763 Genes GS189669: GO:2000112 regulation of cellular macromolecule biosynthetic process
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human GO 2896 Genes GS206108: GO:2001141 regulation of RNA biosynthetic process
Expand Tier I Mouse MP 22 Genes GS166388: MP:0006068 abnormal horizontal cell morphology
Expand Tier I Mouse GO 4353 Genes GS192017: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 137 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 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 739 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human 46 Genes GS174869: HP:0000551 Abnormality of color vision
Expand Tier I Mouse GO 3080 Genes GS177265: GO:0048731 system development
Expand Tier I Human GO 4169 Genes GS207925: GO:0034645 cellular macromolecule biosynthetic process
Expand Tier I Mouse GO 3599 Genes GS186227: GO:0090304 nucleic acid metabolic process
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Mouse GO 3865 Genes GS193238: GO:0031323 regulation of cellular metabolic process
Expand Tier I Human 592 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human GO 3917 Genes GS203908: GO:0016070 RNA metabolic process
Expand Tier I Mouse GO 2955 Genes GS181893: GO:0048522 positive regulation of cellular process
Expand Tier I Human GO 204 Genes GS210485: GO:0007601 visual perception
Expand Tier I Human GO 4811 Genes GS204612: GO:0019222 regulation of metabolic process
Expand Tier I Mouse GO 3597 Genes GS188142: GO:0048856 anatomical structure development
Expand Tier I Mouse 973 Genes GS136531: prion resistance 2 (Prnr2, Published QTL Chr 7)
Expand Tier I Mouse MP 18 Genes GS167528: MP:0008519 thin retinal outer plexiform layer
Expand Tier I Human 392 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Human 140 Genes GS174860: HP:0010549 Paralysis due to lesions of the principle motor tracts
Expand Tier I Mouse MP 96 Genes GS166313: MP:0008450 retinal photoreceptor degeneration
Expand Tier I Human GO 2098 Genes GS209551: GO:0031981 nuclear lumen
Expand Tier I Mouse 831 Genes GS136728: susceptibility to lung cancer 30 (Sluc30, Published QTL Chr 7)
Expand Tier I Mouse MP 9 Genes GS168142: MP:0008583 absent photoreceptor inner segment
Expand Tier I Human GO 2764 Genes GS194555: GO:0031974 membrane-enclosed lumen
Expand Tier I Mouse GO 4114 Genes GS193414: GO:0044249 cellular biosynthetic process
Expand Tier I Human 344 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human GO 818 Genes GS197472: GO:0044451 nucleoplasm part
Expand Tier I Human GO 495 Genes GS209225: GO:0007600 sensory perception
Expand Tier I Human GO 236 Genes GS203525: GO:0043010 camera-type eye development
Expand Tier I Human GO 3573 Genes GS203607: GO:0034654 nucleobase-containing compound biosynthetic process
Expand Tier I Mouse MP 1385 Genes GS163971: MP:0002092 abnormal eye morphology
Expand Tier I Human CTD 5725 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 416 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier I Mouse 266 Genes GS129070: allergen-induced bronchial hyperresponsiveness 3 (Abhr3 Published QTL Chr 7)
Expand Tier I Mouse 973 Genes GS136264: modifier of mammary tumor progression 1 (Mmtp1, Published QTL Chr 7)
Expand Tier I Human 77 Genes GS173703: HP:0000842 Hyperinsulinemia
Expand Tier I Mouse GO 8414 Genes GS185585: GO:0044710 single-organism metabolic process
Expand Tier I Mouse GO 9323 Genes GS180152: GO:0065007 biological regulation
Expand Tier I Mouse MP 331 Genes GS163432: MP:0006069 abnormal retinal neuronal layer morphology
Expand Tier I Mouse GO 763 Genes GS178922: GO:0003700 sequence-specific DNA binding transcription factor activity
Expand Tier I Human 103 Genes GS173741: HP:0100699 Scarring
Expand Tier I Human 97 Genes GS173091: HP:0004374 Hemiplegia/hemiparesis
Expand Tier I Mouse GO 1832 Genes GS187708: GO:0009893 positive regulation of metabolic process
Expand Tier I Mouse 585 Genes GS136233: mandible length 7 (Manln7, Published QTL Chr 7)
Expand Tier I Human GO 1008 Genes GS204232: GO:0001071 nucleic acid binding transcription factor activity
Expand Tier I Mouse MP 574 Genes GS166743: MP:0002229 neurodegeneration
Expand Tier I Mouse GO 2279 Genes GS186488: GO:0048513 organ development
Expand Tier I Human 398 Genes GS172134: HP:0000639 Nystagmus
Expand Tier II Mouse 419 Genes GS36763: Cerebellum Gene expression correlates of Vocalization Threshold - shock intensity (mA) in Males BXD
Expand Tier I Mouse MP 3543 Genes GS169095: MP:0004924 abnormal behavior
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 79 Genes GS175373: HP:0011486 Abnormality of corneal thickness
Expand Tier I Human 578 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Mouse MP 90 Genes GS170245: MP:0004022 abnormal cone electrophysiology
Expand Tier I Mouse 984 Genes GS135458: bone mineral density 4 (Bomd4, Published QTL Chr 7)
Expand Tier I Human 492 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Human 438 Genes GS173024: HP:0000811 Abnormal external genitalia
Expand Tier I Human GO 4567 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 Mouse GO 591 Genes GS182595: GO:0019904 protein domain specific binding
Expand Tier I Human GO 1393 Genes GS193937: GO:0006366 transcription from RNA polymerase II promoter
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 4713 Genes GS205364: GO:0010467 gene expression
Expand Tier I Mouse MP 44 Genes GS163166: MP:0006073 abnormal retinal bipolar cell morphology
Expand Tier I Human 534 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier I Human 36 Genes GS174701: HP:0000556 Retinal dystrophy
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human GO 2332 Genes GS195643: GO:0003677 DNA binding
Expand Tier I Human 5 Genes GS176096: HP:0000548 Cone-rod dystrophy
Expand Tier I Human GO 1842 Genes GS198572: GO:0010604 positive regulation of macromolecule metabolic process
Expand Tier I Human GO 5152 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Tier I Mouse GO 4286 Genes GS190949: GO:0009058 biosynthetic process
Expand Tier I Mouse 2121 Genes GS128593: Average rotarod training latency Chr# 7
Expand Tier I Mouse GO 1176 Genes GS182705: GO:0051173 positive regulation of nitrogen compound metabolic process
Expand Tier I Human GO 999 Genes GS195340: GO:0045893 positive regulation of transcription, DNA-dependent
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Mouse 831 Genes GS136263: modifier of mammary tumor growth 3 (Mmtg3, Published QTL Chr 7)
Expand Tier I Human 384 Genes GS171708: HP:0000359 Abnormality of the inner ear
Expand Tier I Mouse MP 574 Genes GS167217: MP:0001325 abnormal retina morphology
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Human GO 1693 Genes GS209960: GO:0003008 system process
Expand Tier III Rat 875 Genes GS216492: Genes that are binding sites for CREB and zif268, transcription factors mediating neuronal activity and plasticity, in Rattus norvegicus.
Expand Tier I Mouse MP 3543 Genes GS169828: MP:0005386 behavior/neurological phenotype
Expand Tier I Human 179 Genes GS171047: HP:0008736 Hypoplasia of penis
Expand Tier I Human 274 Genes GS172372: HP:0000648 Optic atrophy
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human GO 1279 Genes GS201265: GO:0009891 positive regulation of biosynthetic process
Expand Tier I Mouse GO 3005 Genes GS177308: GO:1901362 organic cyclic compound biosynthetic process
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Mouse GO 286 Genes GS190016: GO:0001654 eye development
Expand Tier I Human 170 Genes GS173988: HP:0000501 Glaucoma
Expand Tier I Human GO 3118 Genes GS206544: GO:2000112 regulation of cellular macromolecule biosynthetic process
Expand Tier I Mouse GO 3021 Genes GS182703: GO:0051171 regulation of nitrogen compound metabolic process
Expand Tier I Human GO 1256 Genes GS210178: GO:0031328 positive regulation of cellular biosynthetic process
Expand Tier I Human 249 Genes GS176844: HP:0000429 Abnormality of the nasal alae
Expand Tier I Mouse GO 284 Genes GS182194: GO:0005667 transcription factor complex
Expand Tier I Human GO 6278 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human GO 275 Genes GS206897: GO:0001654 eye development
Expand Tier I Mouse MP 140 Genes GS169804: MP:0003731 abnormal retinal outer nuclear layer morphology
Expand Tier I Mouse MP 983 Genes GS166244: MP:0002752 abnormal somatic nervous system morphology
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 8137 Genes GS202316: GO:0050789 regulation of biological process
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human 281 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 2050 Genes GS203406: GO:0009653 anatomical structure morphogenesis
Expand Tier I Human 100 Genes GS176744: HP:0000987 Atypical scarring of skin
Expand Tier I Mouse GO 1260 Genes GS184461: GO:0009891 positive regulation of biosynthetic process
Expand Tier I Mouse 1023 Genes GS136742: Streptococcus pneumoniae infection resistance 1 (Spir1, Published QTL Chr 7)
Expand Tier I Human 89 Genes GS176988: HP:0008046 Abnormality of the retinal vasculature
Expand Tier I Mouse GO 4500 Genes GS186790: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Mouse GO 1763 Genes GS178885: GO:0003677 DNA binding
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 5452 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Human GO 1198 Genes GS199501: GO:0051173 positive regulation of nitrogen compound metabolic process
Expand Tier I Human 403 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Human 202 Genes GS171631: HP:0008051 Abnormality of the retinal pigment epithelium
Expand Tier I Mouse GO 4588 Genes GS177309: GO:1901363 heterocyclic compound binding
Expand Tier I Human GO 4151 Genes GS206329: GO:0060255 regulation of macromolecule metabolic process
Expand Tier I Mouse MP 126 Genes GS163943: MP:0005201 abnormal retinal pigment epithelium morphology
Expand Tier I Human 174 Genes GS173019: HP:0000819 Diabetes mellitus
Expand Tier I Mouse GO 2595 Genes GS188410: GO:0032774 RNA biosynthetic process
Expand Tier I Mouse MP 92 Genes GS170195: MP:0008515 thin retinal outer nuclear layer
Expand Tier I Human GO 5948 Genes GS195199: GO:0005634 nucleus
Expand Tier I Mouse MP 585 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 GO 9049 Genes GS180166: GO:0008152 metabolic process
Expand Tier I Mouse GO 1232 Genes GS193234: GO:0031328 positive regulation of cellular biosynthetic process
Expand Tier I Mouse 910 Genes GS135938: HDL level 38 (Hdl38, Published QTL Chr 7)
Expand Tier I Mouse MP 647 Genes GS164446: MP:0005195 abnormal posterior eye segment morphology
Expand Tier I Mouse 910 Genes GS135746: experimental allergic encephalomyelitis susceptibility 12 (Eae12, Published QTL Chr 7)
Expand Tier I Human 136 Genes GS171855: HP:0000597 Ophthalmoparesis
Expand Tier I Mouse MP 3716 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier I Human GO 8 Genes GS197112: GO:0043522 leucine zipper domain binding
Expand Tier I Mouse MP 48 Genes GS169803: MP:0003730 abnormal photoreceptor inner segment morphology
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 290 Genes GS198991: GO:0005667 transcription factor complex
Expand Tier I Human 123 Genes GS171946: HP:0002269 Abnormality of neuronal migration
Expand Tier I Human 358 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Mouse GO 690 Genes GS180673: GO:0044451 nucleoplasm part
Expand Tier I Human 472 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Mouse GO 2540 Genes GS189240: GO:2001141 regulation of RNA biosynthetic process
Expand Tier I Human GO 4446 Genes GS203072: GO:0090304 nucleic acid metabolic process
Expand Tier I Mouse MP 169 Genes GS166016: MP:0001324 abnormal eye pigmentation
Expand Tier I Mouse 1027 Genes GS128580: BECs at LORR Recovery Chr# 7
Expand Tier I Mouse GO 1149 Genes GS186178: GO:0045935 positive regulation of nucleobase-containing compound metabolic process
Expand Tier I Mouse GO 8386 Genes GS189751: GO:0050794 regulation of cellular process
Expand Tier I Mouse GO 4637 Genes GS177382: GO:0097159 organic cyclic compound binding
Expand Tier I Mouse MP 106 Genes GS166716: MP:0003729 abnormal photoreceptor outer segment morphology
Expand Tier I Human GO 1006 Genes GS195678: GO:0003700 sequence-specific DNA binding transcription factor activity
Expand Tier I Human 551 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Mouse GO 2588 Genes GS187343: GO:0006351 transcription, DNA-dependent
Expand Tier I Mouse 973 Genes GS135988: Hfe modifier 1 (Hfem1, Published QTL Chr 7)
Expand Tier I Human 364 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human GO 1477 Genes GS203369: GO:0005654 nucleoplasm
Expand Tier I Mouse MP 1476 Genes GS169531: MP:0005391 vision/eye phenotype
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 699 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 544 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 472 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Mouse GO 10879 Genes GS181473: GO:0005488 binding
Expand Tier I Human GO 2673 Genes GS205543: GO:0070013 intracellular organelle lumen
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Mouse GO 1777 Genes GS184445: GO:0044428 nuclear part
Expand Tier I Human 512 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 1087 Genes GS192345: GO:0010628 positive regulation of gene expression
Expand Tier I Human GO 8622 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human GO 3401 Genes GS200312: GO:0019219 regulation of nucleobase-containing compound metabolic process
Expand Tier I Mouse GO 8 Genes GS180330: GO:0043522 leucine zipper domain binding
Expand Tier I Mouse MP 592 Genes GS165809: MP:0002864 abnormal ocular fundus morphology
Expand Tier I Mouse GO 4518 Genes GS187751: GO:0019222 regulation of metabolic process
Expand Tier I Mouse GO 713 Genes GS177859: GO:0045944 positive regulation of transcription from RNA polymerase II promoter
Expand Tier I Mouse GO 1147 Genes GS191150: GO:0010557 positive regulation of macromolecule biosynthetic process
Expand Tier I Human 221 Genes GS171139: HP:0005288 Abnormality of the nares
Expand Tier I Mouse GO 1715 Genes GS193237: GO:0031325 positive regulation of cellular metabolic process
Expand Tier I Human 616 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse GO 4333 Genes GS184452: GO:0044422 organelle part
Expand Tier I Human GO 3201 Genes GS204204: GO:0006351 transcription, DNA-dependent
Expand Tier I Human 149 Genes GS172295: HP:0001513 Obesity
Expand Tier I Mouse GO 4073 Genes GS180034: GO:0032502 developmental process
Expand Tier I Human GO 6651 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Mouse 940 Genes GS135417: beta-carboline induced seizures 4 (Bis4, Published QTL Chr 7)
Expand Tier I Human 534 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier I Human GO 688 Genes GS194602: GO:0045944 positive regulation of transcription from RNA polymerase II promoter
Expand Tier I Human GO 4314 Genes GS204746: GO:0080090 regulation of primary metabolic process
Expand Tier I Mouse MP 47 Genes GS166824: MP:0005103 abnormal retinal pigmentation
Expand Tier I Human GO 2486 Genes GS201249: GO:0044428 nuclear part
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Mouse GO 2598 Genes GS185259: GO:0051252 regulation of RNA metabolic process
Expand Tier I Human GO 5379 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 3513 Genes GS193991: GO:0048731 system development
Expand Tier I Human 381 Genes GS175714: HP:0011389 Functional abnormality of the inner ear
Expand Tier I Human GO 3626 Genes GS198456: GO:0019438 aromatic compound biosynthetic process
Expand Tier I Human GO 5601 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Human GO 105 Genes GS204694: GO:0060041 retina development in camera-type eye
Expand Tier I Mouse 641 Genes GS136214: lupus BXSB x NZW 6 (Lxw6, Published QTL Chr 7)
Expand Tier I Mouse MP 174 Genes GS169334: MP:0009389 abnormal extracutaneous pigmentation
Expand Tier I Mouse GO 2907 Genes GS181667: GO:0019438 aromatic compound biosynthetic process
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human 188 Genes GS171512: HP:0007703 Abnormal retinal pigmentation
Expand Tier I Human GO 5558 Genes GS194040: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Human GO 3310 Genes GS194088: GO:0003676 nucleic acid binding
Expand Tier I Human 416 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Mouse GO 3090 Genes GS188511: GO:0010468 regulation of gene expression
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human 183 Genes GS176955: HP:0000431 Wide nasal bridge
Expand Tier I Mouse GO 2917 Genes GS190067: GO:0018130 heterocycle biosynthetic process
Expand Tier I Human 368 Genes GS170971: HP:0000407 Sensorineural hearing impairment
Expand Tier I Human 445 Genes GS175423: HP:0010461 Abnormality of the male genitalia
Expand Tier I Mouse MP 466 Genes GS163138: MP:0005253 abnormal eye physiology
Expand Tier I Human GO 3287 Genes GS205266: GO:0032774 RNA biosynthetic process
Expand Tier I Human 120 Genes GS171657: HP:0000613 Photophobia
Expand Tier I Human 913 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Mouse GO 994 Genes GS178589: GO:0045893 positive regulation of transcription, DNA-dependent
Expand Tier I Mouse 593 Genes GS136894: ventricular size 3 (Vent3, Published QTL Chr 7)
Expand Tier III Mouse 8392 Genes GS128199: Alcohol Preference union of 86 Gene Sets
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Mouse GO 628 Genes GS179777: GO:0043565 sequence-specific DNA binding
Expand Tier I Human 64 Genes GS172899: HP:0011815 Cephalocele
Expand Tier I Mouse 1024 Genes GS136253: modifier of Dlk1 (mdlk1, Published QTL Chr 7)
Expand Tier I Mouse MP 96 Genes GS164692: MP:0004021 abnormal rod electrophysiology
Expand Tier I Human 308 Genes GS172100: HP:0000587 Abnormality of the optic nerve
Expand Tier I Mouse GO 2947 Genes GS193236: GO:0031326 regulation of cellular biosynthetic process
Expand Tier I Human GO 7311 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human GO 5047 Genes GS210357: GO:0044249 cellular biosynthetic process
Expand Tier I Human 320 Genes GS175597: HP:0011013 Abnormality of carbohydrate metabolism/homeostasis
Expand Tier I Mouse GO 7552 Genes GS180452: GO:0044237 cellular metabolic process
Expand Tier I Human 384 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 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 Mouse 585 Genes GS136096: long bones 6 (Lbn6, Published QTL Chr 7)
Expand Tier I Mouse GO 2991 Genes GS182469: GO:0043234 protein complex
Expand Tier I Human GO 3640 Genes GS206953: GO:0018130 heterocycle biosynthetic process
Expand Tier I Mouse 940 Genes GS136189: lipoprotein QTL 5 (Lprq5, Published QTL Chr 7)
Expand Tier I Mouse GO 3382 Genes GS191021: GO:0034645 cellular macromolecule biosynthetic process
Expand Tier I Human GO 3487 Genes GS199499: GO:0051171 regulation of nitrogen compound metabolic process
Expand Tier I Mouse GO 106 Genes GS187835: GO:0060041 retina development in camera-type eye
Expand Tier I Human GO 3446 Genes GS203057: GO:0048518 positive regulation of biological process
Expand Tier II Mouse 929 Genes GS84191: alcohol preference 7 QTL (Ap7q, Published QTL, Chr 7)
Expand Tier I Human GO 2545 Genes GS203335: GO:0048513 organ development
Expand Tier I Human 201 Genes GS176660: HP:0000050 Hypoplastic genitalia
Expand Tier I Mouse GO 1582 Genes GS188684: GO:0070013 intracellular organelle lumen
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Human GO 3721 Genes GS194499: GO:0044271 cellular nitrogen compound biosynthetic process
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Human 384 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Mouse GO 2595 Genes GS177357: GO:0003676 nucleic acid binding
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Mouse GO 6435 Genes GS177531: GO:0043170 macromolecule metabolic process
Expand Tier I Mouse MP 226 Genes GS169032: MP:0005551 abnormal eye electrophysiology
Expand Tier I Human 65 Genes GS171651: HP:0000618 Blindness
Expand Tier I Human GO 680 Genes GS196540: GO:0043565 sequence-specific DNA binding
Expand Tier I Mouse GO 245 Genes GS186677: GO:0043010 camera-type eye development
Expand Tier I Mouse MP 23 Genes GS168576: MP:0008585 absent photoreceptor outer segment
Expand Tier I Human GO 8702 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 990 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Mouse GO 1208 Genes GS177214: GO:0006366 transcription from RNA polymerase II promoter
Expand Tier I Mouse GO 3583 Genes GS180236: GO:0032991 macromolecular complex
Expand Tier I Mouse GO 1587 Genes GS182475: GO:0043233 organelle lumen
Expand Tier I Human GO 4276 Genes GS207858: GO:0009059 macromolecule biosynthetic process
Expand Tier I Mouse GO 3978 Genes GS188506: GO:0010467 gene expression
Expand Tier I Mouse MP 5 Genes GS164848: MP:0006075 abnormal retinal cone bipolar cell morphology
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Mouse 585 Genes GS136238: mandible size 5 (Manz5, Published QTL Chr 7)
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human GO 2875 Genes GS195291: GO:0006355 regulation of transcription, DNA-dependent
Expand Tier I Human GO 5369 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier I Human GO 3344 Genes GS205369: GO:0010468 regulation of gene expression
Expand Tier I Mouse GO 4218 Genes GS192073: GO:1901576 organic substance biosynthetic process
Expand Tier I Mouse MP 2200 Genes GS165465: MP:0003633 abnormal nervous system physiology
Expand Tier I Human 388 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Mouse GO 7644 Genes GS188399: GO:0044238 primary metabolic process
Expand Tier I Human 514 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Mouse GO 2984 Genes GS188762: GO:0009889 regulation of biosynthetic process
Expand Tier I Human GO 7689 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier I Mouse GO 1628 Genes GS177813: GO:0031974 membrane-enclosed lumen
Expand Tier I Mouse GO 8072 Genes GS184218: GO:0071704 organic substance metabolic process
Expand Tier I Mouse GO 1381 Genes GS192610: GO:0031981 nuclear lumen
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 Mouse GO 4478 Genes GS184435: GO:0046483 heterocycle metabolic process
Expand Tier I Human 3 Genes GS175610: HP:0007994 Peripheral visual field loss
Expand Tier I Mouse GO 765 Genes GS187370: GO:0001071 nucleic acid binding transcription factor activity
Expand Tier I Human GO 14 Genes GS200472: GO:0030275 LRR domain binding
Expand Tier I Mouse GO 3293 Genes GS186214: GO:0048518 positive regulation of biological process
Expand Tier I Human GO 3737 Genes GS194038: GO:1901362 organic cyclic compound biosynthetic process
Expand Tier I Human 64 Genes GS174379: HP:0002084 Encephalocele
Expand Tier I Mouse MP 37 Genes GS170724: MP:0002561 abnormal circadian phase
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 232 Genes GS176771: HP:0001000 Abnormality of skin pigmentation
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 414 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Mouse 901 Genes GS135415: bronchial hyperresponsiveness 6 (Bhr6, Published QTL Chr 7)
Expand Tier I Human 92 Genes GS171656: HP:0000610 Abnormality of the choroid
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Mouse GO 4651 Genes GS177310: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Human 1228 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human GO 3324 Genes GS210180: GO:0031326 regulation of cellular biosynthetic process
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Human GO 3354 Genes GS205622: GO:0009889 regulation of biosynthetic process
Expand Tier I Mouse MP 136 Genes GS163942: MP:0005200 abnormal eye pigment epithelium morphology
Expand Tier I Mouse GO 2835 Genes GS191151: GO:0010556 regulation of macromolecule biosynthetic process
Expand Tier I Human GO 1079 Genes GS209282: GO:0010628 positive regulation of gene expression
Expand Tier I Mouse GO 3757 Genes GS189460: GO:0060255 regulation of macromolecule metabolic process
Expand Tier I Human GO 3861 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Mouse GO 5247 Genes GS178448: GO:0005634 nucleus
Expand Tier I Human 291 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier I Human 1006 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 489 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Mouse MP 710 Genes GS167922: MP:0000959 abnormal somatic sensory system morphology
Expand Tier I Human GO 3199 Genes GS208061: GO:0010556 regulation of macromolecule biosynthetic process
Expand Tier I Mouse GO 2536 Genes GS178537: GO:0006355 regulation of transcription, DNA-dependent
Expand Tier I Mouse MP 438 Genes GS165390: MP:0003224 neuron degeneration
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Mouse GO 327 Genes GS187984: GO:0003682 chromatin binding
Expand Tier I Human 211 Genes GS173206: HP:0003241 Genital hypoplasia
Expand Tier I Human 157 Genes GS171968: HP:0000405 Conductive hearing impairment
Expand Tier I Human 941 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Mouse 653 Genes GS135679: Crhr1 transcript abundance QTL 1 (Crhr1taq1, Published QTL Chr 7)
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human 158 Genes GS171900: HP:0011452 Functional abnormality of the middle ear
Expand Tier I Mouse MP 14488 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Human GO 541 Genes GS199393: GO:0019904 protein domain specific binding
Expand Tier I Mouse MP 27 Genes GS166481: MP:0008518 retinal outer nuclear layer degeneration
Expand Tier I Mouse MP 18 Genes GS163167: MP:0006074 abnormal retinal rod bipolar cell morphology
Expand Tier I Human 498 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Mouse GO 3136 Genes GS187045: GO:0016070 RNA metabolic process
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human GO 792 Genes GS205616: GO:0009887 organ morphogenesis
Expand Tier I Human GO 4377 Genes GS210182: GO:0031323 regulation of cellular metabolic process
Expand Tier I Human GO 7336 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 416 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier I Human 8 Genes GS171975: HP:0000533 Chorioretinal atrophy
Expand Tier I Human 287 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 2087 Genes GS128573: Ethanol Induced Hypothermia Chr# 7
Expand Tier I Mouse GO 2981 Genes GS177761: GO:0044271 cellular nitrogen compound biosynthetic process
Expand Tier I Mouse 585 Genes GS136298: maternal performance (Mprf, Published QTL Chr 7)
Expand Tier I Human 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Mouse GO 3605 Genes GS190682: GO:0007275 multicellular organismal development
Expand Tier I Human 210 Genes GS175990: HP:0000463 Anteverted nares
Expand Tier I Human GO 3275 Genes GS199267: GO:0043234 protein complex
Expand Tier I Mouse 975 Genes GS136602: sperm beat cross frequency (Sbcf, Published QTL Chr 7)
Expand Tier I Mouse GO 1684 Genes GS181783: GO:0010604 positive regulation of macromolecule metabolic process
Expand Tier I Mouse GO 4224 Genes GS193059: GO:0044446 intracellular organelle part
Expand Tier I Human GO 1880 Genes GS210181: GO:0031325 positive regulation of cellular metabolic process
Expand Tier I Human 96 Genes GS176616: HP:0000662 Night blindness
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse GO 15 Genes GS183669: GO:0030275 LRR domain binding
Expand Tier I Human GO 2957 Genes GS202080: GO:0051252 regulation of RNA metabolic process
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human GO 1981 Genes GS204568: GO:0009893 positive regulation of metabolic process
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 273 Genes GS172516: HP:0001347 Hyperreflexia
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 5962 Genes GS205047: GO:0006807 nitrogen compound metabolic 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