| Type | Description |
|---|---|
| Definition | cytochrome P450 family 4 subfamily V member 2 |
| Date | Results | Publications |
|---|---|---|
| 2021-03-27 14:42:00 | Identification and functional characterization of CYP4V2 genetic variants exhibiting decreased activity of lauric acid metabolism. | 32396266 |
| 2021-01-09 13:34:00 | [Analysis of phenotype and CYP4V2 gene variants in two pedigrees affected with Bietti crystalline corneoretinal dystrophy]. | 33306817 |
| 2020-06-13 11:38:00 | Homozygous mutation in CYP4V2 gene is associated with Bietti's retinal dystrophy. | 31638456 |
| 2020-05-16 12:56:00 | Mutation in the CYP4V2 gene is associated with Bietti's crystalline dystrophy. | 31512983 |
| 2020-04-25 12:05:00 | mutations in CYP4V2 may be common in the Chinese population. | 31741654 |
| Type | IDs |
|---|---|
| Synonymous | BCD, CYP4AH1 |
| Gene |
UniProtKB-ID:
CP4V2_HUMAN
UniprotKB:
Q6ZWL3
UniParc:
UPI00002372FE,
UPI00015E083F
EMBL:
BC060857,
FJ440682,
AK122600,
AK126473,
AC110771,
AY422002
Ensembl:
ENSG00000145476
KO:
hsa:285440
|
| Nucleutide sequences |
EMBL-CDS:
AAR31180.1,
AAH60857.1,
ACK44069.1,
BAC85487.1,
BAC86562.1
Ensembl_TRS:
ENST00000378802
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000368079
RefSeq:
XP_005262992.1,
XP_016863526.1,
NP_997235.3
|
| Others |
UniRef100:
UniRef100_Q6ZWL3
UniRef90:
UniRef90_Q6ZWL3
UniRef50:
UniRef50_Q6ZWL3
UniGene:
Hs.587231
CCDS:
CCDS34119.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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