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 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 1771 Genes GS196284: GO:0012505 endomembrane system
Expand Tier I Human GO 556 Genes GS195139: GO:0055114 oxidation-reduction process
Expand Tier I Human 1 Genes GS175243: HP:0007880 Marginal corneal dystrophy
Expand Tier I Human GO 6769 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier III Human 2187 Genes GS218390: Alcoholism Susceptibility Chr 1
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human 42 Genes GS174449: HP:0001123 Visual field defect
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 414 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human GO 1693 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 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human GO 139 Genes GS194657: GO:0046906 tetrapyrrole binding
Expand Tier I Human GO 9213 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 2511 Genes GS207903: GO:0044281 small molecule metabolic process
Expand Tier I Human GO 6278 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human GO 5436 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 5320 Genes GS207615: GO:0016021 integral to membrane
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 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human GO 810 Genes GS195897: GO:0044255 cellular lipid metabolic process
Expand Tier I Human GO 5400 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Human 34 Genes GS174909: HP:0000546 Retinal degeneration
Expand Tier I Human GO 403 Genes GS199550: GO:0032787 monocarboxylic acid metabolic process
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 5810 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human GO 2373 Genes GS195036: GO:0031090 organelle membrane
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human GO 8702 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 33 Genes GS174652: HP:0001131 Corneal dystrophy
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human GO 1281 Genes GS196726: GO:0005783 endoplasmic reticulum
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human GO 6151 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human GO 4034 Genes GS208978: GO:0043169 cation binding
Expand Tier I Human CTD 85 Genes GS124857: perfluorooctane sulfonic acid interacting genes (MeSH:C076994) in CTD
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human GO 971 Genes GS210163: GO:0006082 organic acid metabolic process
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 5321 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 2 Genes GS200454: GO:0010430 fatty acid omega-oxidation
Expand Tier I Human 512 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Human GO 1138 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 324 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human GO 7808 Genes GS207616: GO:0016020 membrane
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human 1 Genes GS174794: HP:0007675 Progressive night blindness
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human GO 709 Genes GS198755: GO:0016491 oxidoreductase activity
Expand Tier I Human 626 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 772 Genes GS196729: GO:0005789 endoplasmic reticulum membrane
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 Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 162 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 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 919 Genes GS197025: GO:0044432 endoplasmic reticulum part
Expand Tier I Human GO 279 Genes GS198219: GO:0006631 fatty acid metabolic process
Expand Tier I Human GO 130 Genes GS199478: GO:0020037 heme binding
Expand Tier I Human GO 3934 Genes GS198323: GO:0046872 metal ion binding
Expand Tier I Human GO 92 Genes GS194937: GO:0034440 lipid oxidation
Expand Tier I Human GO 789 Genes GS204928: GO:0042175 nuclear outer membrane-endoplasmic reticulum membrane network
Expand Tier I Human GO 846 Genes GS204326: GO:0019752 carboxylic acid metabolic process
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 953 Genes GS202555: GO:0043436 oxoacid metabolic process
Expand Tier I Human GO 168 Genes GS197078: GO:0005506 iron ion 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 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 145 Genes GS209189: GO:0030258 lipid modification
Expand Tier I Human GO 2241 Genes GS209291: GO:0046914 transition metal ion binding
Expand Tier I Human CTD 4389 Genes GS123768: Cyclosporine interacting genes (MeSH:D016572) in CTD