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1589 CYP21A2

1589

CYP21A2

cytochrome P450 family 21 subfamily A member 2

protein-coding

Homo sapiens

基因描述

Type Description
Definition cytochrome P450 family 21 subfamily A member 2

研究结论

Date Results Publications
2021-03-20 13:26:00 Simple virilising congenital adrenal hyperplasia in monozygotic twins: A rare report and review of previous cases.", trans "Wrodzony przerost nadnerczy z prosta wirylizacja u blizniat monozygotycznych: opis rzadkiego przypadku i przeglad wczesniejszych przypadkow. 32272826
2021-03-13 13:25:00 [Clinical characteristics of 21 infertile women with non-classic 21-hydroxylase deficiency]. 33631882
2020-12-05 13:02:00 21-Hydroxylase deficiency: Mutational spectrum and Genotype-Phenotype relations analyses by next-generation sequencing and multiplex ligation-dependent probe amplification. 31586465
2020-11-28 13:16:00 A novel function of CYP21A2 in regulating cell migration and invasion via Wnt signaling. 32902406
2020-11-21 13:34:00 [Correlation between variants of CYP21A2 gene promoter region and nonclassical 21-hydroxylase deficiency]. 32761585

名称对应

Type IDs
Synonymous CA21H, CAH1, CPS1, CYP21, CYP21B, P450c21B
Gene
UniProtKB-ID: CP21A_HUMAN, Q16874_HUMAN, Q08AG9_HUMAN
UniprotKB: P08686, Q16874, Q08AG9
UniParc: UPI000011D64D, UPI0002B8CC01, UPI0000073F52, UPI0000E44809
EMBL: GQ222340, AL844853, BC125181, KU302773, GQ222320, JN034411, JN034403, GQ222286, GQ222289, GQ222323, CR753845, AF019413, GQ222278, GQ222334, AL049547, AL929593, JN034401, AL645922, GQ222296, KU302772, GQ222295, JN034410, X58906, JN034397, BC125182, BX679671, GQ222321, GQ222297, GQ222327, CR936924, CH471081, AL662849, JN034395, AK054616, M19711, JN034391, JN034394, AL662828, JN034393, JN034402, GQ222312, M13936, GQ222283, GQ222301, GQ222319, JN034398, M12792, JN034396, KC493622, AK314651, M17252, M26856, K02771
Ensembl: ENSG00000232414, ENSG00000233151, ENSG00000235134, ENSG00000206338, ENSG00000231852, ENSG00000198457
KO: hsa:1589
Nucleutide sequences
EMBL-CDS: AAA52064.1, AAA59985.1, ACT35422.1, AAA59706.1, ACT35427.1, CAA41709.1, AAI25183.1, AAB59440.1, EAX03570.1, AAA59695.1, BAB70774.1, AAA83248.1, ACT35412.1, AHA59281.1, ACT35447.1, AFK10126.1, EAX03571.1, BAG37212.1, ACT35445.1, ACT35423.1, ACT35421.1, CAB89301.1, AFK10121.1, AFK10134.1, AFK10116.1, ACT35466.1, ACT35453.1, APT40592.1, AFK10125.1, ACT35409.1, AFK10124.1, ACT35449.1, ACT35404.1, AFK10117.1, ACT35446.1, ACT35438.1, AFK10118.1, AFK10119.1, ACT35460.1, AFK10120.1, AAB67982.1, ACT35415.1, APT40591.1, AFK10114.1, AFK10133.1, AAI25182.1
Gene_ORFName: hCG_1999926
Ensembl_TRS: ENST00000435122, ENST00000383321, ENST00000436607, ENST00000448314, ENST00000434026, ENST00000452386, ENST00000383322, ENST00000644719, ENST00000456152, ENST00000448478
Protein sequencees
Ensembl_PRO: ENSP00000392321, ENSP00000415043, ENSP00000372811, ENSP00000403721, ENSP00000398594, ENSP00000403230, ENSP00000416598, ENSP00000394942, ENSP00000372812, ENSP00000496625
RefSeq: NP_001122062.3, NP_001355072.1, XP_024308323.1, NP_001355073.1, NP_000491.4
Others
UniRef100: UniRef100_P08686, UniRef100_Q16874, UniRef100_Q08AG9
UniRef90: UniRef90_P08686
UniRef50: UniRef50_P08686
UniGene: Hs.654479
CCDS: CCDS47406.1

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