Gene Details



CYP4V2 and homologs in 1 species are found in 96 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 Human GO 10576 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 1762 Genes GS196284: GO:0012505 endomembrane system
Expand Tier I Human GO 555 Genes GS195139: GO:0055114 oxidation-reduction process
Expand Tier I Human 1 Genes GS175243: HP:0007880 Marginal corneal dystrophy
Expand Tier I Human GO 6743 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier III Human 2616 Genes GS218390: Alcoholism Susceptibility Chr 1
Expand Tier I Human GO 7609 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human 42 Genes GS174449: HP:0001123 Visual field defect
Expand Tier I Human GO 5623 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 411 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human GO 1691 Genes GS209960: GO:0003008 system process
Expand Tier I Human CTD 1601 Genes GS123916: Aflatoxin B1 interacting genes (MeSH:D016604) in CTD
Expand Tier I Human 92 Genes GS171656: HP:0000610 Abnormality of the choroid
Expand Tier I Human GO 9526 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human GO 138 Genes GS194657: GO:0046906 tetrapyrrole binding
Expand Tier I Human GO 9155 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human GO 93 Genes GS206081: GO:0004497 monooxygenase activity
Expand Tier I Human GO 2509 Genes GS207903: GO:0044281 small molecule metabolic process
Expand Tier I Human GO 6256 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human GO 15151 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 9088 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human GO 5359 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Human GO 89 Genes GS200759: GO:0019395 fatty acid oxidation
Expand Tier I Human GO 5243 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 5400 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human GO 809 Genes GS195897: GO:0044255 cellular lipid metabolic process
Expand Tier I Human GO 5348 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Human 34 Genes GS174909: HP:0000546 Retinal degeneration
Expand Tier I Human GO 402 Genes GS199550: GO:0032787 monocarboxylic acid metabolic process
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 5764 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human 33 Genes GS174652: HP:0001131 Corneal dystrophy
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human CTD 6287 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human CTD 85 Genes GS124857: perfluorooctane sulfonic acid interacting genes (MeSH:C076994) in CTD
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
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 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 GO 1137 Genes GS193812: GO:0006629 lipid metabolic process
Expand Tier I Human GO 157 Genes GS207864: GO:0009055 electron carrier activity
Expand Tier I Human GO 205 Genes GS209987: GO:0050953 sensory perception of light stimulus
Expand Tier I Human 323 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier I Human GO 8948 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human GO 7717 Genes GS207616: GO:0016020 membrane
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human 1 Genes GS174794: HP:0007675 Progressive night blindness
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human GO 706 Genes GS198755: GO:0016491 oxidoreductase activity
Expand Tier I Human 621 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Human GO 204 Genes GS210485: GO:0007601 visual perception
Expand Tier I Human GO 768 Genes GS196729: GO:0005789 endoplasmic reticulum membrane
Expand Tier I Human 95 Genes GS176616: HP:0000662 Night blindness
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 161 Genes GS202464: GO:0016705 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
Expand Tier I Human 12 Genes GS174650: HP:0001133 Constricted visual fields
Expand Tier I Human CTD 355 Genes GS123990: perfluorooctanoic acid interacting genes (MeSH:C023036) in CTD
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 915 Genes GS197025: GO:0044432 endoplasmic reticulum part
Expand Tier I Human GO 278 Genes GS198219: GO:0006631 fatty acid metabolic process
Expand Tier I Human GO 129 Genes GS199478: GO:0020037 heme binding
Expand Tier I Human GO 3902 Genes GS198323: GO:0046872 metal ion binding
Expand Tier I Human GO 92 Genes GS194937: GO:0034440 lipid oxidation
Expand Tier I Human GO 785 Genes GS204928: GO:0042175 nuclear outer membrane-endoplasmic reticulum membrane network
Expand Tier I Human GO 845 Genes GS204326: GO:0019752 carboxylic acid metabolic process
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 952 Genes GS202555: GO:0043436 oxoacid metabolic process
Expand Tier I Human GO 167 Genes GS197078: GO:0005506 iron ion binding
Expand Tier I Human GO 493 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 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 GO 144 Genes GS209189: GO:0030258 lipid modification
Expand Tier I Human GO 2216 Genes GS209291: GO:0046914 transition metal ion binding
Expand Tier I Human CTD 4391 Genes GS123768: Cyclosporine interacting genes (MeSH:D016572) in CTD
Expand Tier I Human GO 2361 Genes GS195036: GO:0031090 organelle membrane
Expand Tier I Human GO 8645 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human GO 1276 Genes GS196726: GO:0005783 endoplasmic reticulum
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
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 GO 4003 Genes GS208978: GO:0043169 cation binding
Expand Tier I Human GO 970 Genes GS210163: GO:0006082 organic acid metabolic process
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 GO 5280 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Human GO 2 Genes GS200454: GO:0010430 fatty acid omega-oxidation