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4208 MEF2C

4208

MEF2C

myocyte enhancer factor 2C

protein-coding

Homo sapiens

基因描述

Type Description
Definition myocyte enhancer factor 2C

研究结论

Date Results Publications
2021-01-23 12:56:00 Methylationassociated silencing of miR638 promotes endometrial carcinoma progression by targeting MEF2C. 32186750
2021-01-16 16:01:00 Interaction of OIP5-AS1 with MEF2C mRNA promotes myogenic gene expression. 33270893
2020-11-28 13:15:00 High expression of myocyte enhancer factor 2C predicts poor prognosis for adult acute myeloid leukaemia with normal karyotype. 32017034
2020-07-25 10:40:00 MEF2C is associated with ADHD risk. 32046534
2020-06-27 10:04:00 homeostasis and physiological function of AQP1 in endothelial health are maintained by the MEF2C and miR-133a-3p.1 regulatory circuit 31254364

名称对应

Type IDs
Synonymous C5DELq14.3, DEL5q14.3
Gene
UniProtKB-ID: MEF2C_HUMAN, A0A024RAL7_HUMAN, D8L7E9_HUMAN, A0A0D9SGI5_HUMAN, A0A024RAL6_HUMAN
UniprotKB: Q06413, A0A024RAL7, D8L7E9, A0A0D9SGI5, A0A024RAL6
UniParc: UPI0000D9B539, UPI000002ADD8, UPI000002ADD9, UPI0000040635, UPI00005A05DC, UPI0001D92066, UPI00005A05D7, UPI0001DC9A70
EMBL: AC008525, FM163484, CH471084, FM180475, S57212, AL833268, AL833274, AC008835, L08895
Ensembl: ENSG00000081189
KO: hsa:4208
Nucleutide sequences
EMBL-CDS: CAQ57795.2, AAB25838.1, AAA59578.1, EAW95962.1, EAW95968.1, CAQ86609.1, EAW95963.1, EAW95961.1
Gene_ORFName: hCG_36839, hCG_36839
Ensembl_TRS: ENST00000628656, ENST00000636998, ENST00000508569, ENST00000629612, ENST00000637732, ENST00000514028, ENST00000424173, ENST00000625674, ENST00000437473, ENST00000504921, ENST00000636294, ENST00000514015, ENST00000340208, ENST00000626391, ENST00000625585
Protein sequencees
Ensembl_PRO: ENSP00000487311, ENSP00000340874, ENSP00000423597, ENSP00000487430, ENSP00000421925, ENSP00000389610, ENSP00000424606, ENSP00000426665, ENSP00000490473, ENSP00000490241, ENSP00000486554, ENSP00000490630, ENSP00000396219, ENSP00000487184, ENSP00000487538
RefSeq: NP_001351275.1, NP_001351260.1, NP_001351276.1, NP_001351285.1, NP_001350510.1, XP_011541698.1, NP_001351274.1, NP_001351271.1, NP_001294931.1, NP_001351279.1, NP_001180278.1, NP_001351283.1, NP_001351282.1, NP_001351278.1, XP_024301827.1, NP_001351262.1, NP_001351269.1, XP_016864964.1, NP_001351258.1, NP_001351277.1, NP_001351261.1, NP_001351263.1, XP_024301826.1, NP_001351268.1, NP_001180276.1, NP_001351284.1, NP_001351270.1, NP_001351265.1, XP_005248568.1, NP_001180277.1, XP_011541699.1, XP_024301823.1, NP_001351264.1, NP_001351272.1, NP_001351281.1, NP_001351259.1, NP_001351286.1, XP_006714688.1, NP_001351273.1, NP_001351267.1, XP_016864967.1, XP_024301825.1, XP_024301824.1, NP_001124477.1, NP_001180279.1, NP_002388.2, NP_001351266.1
Others
UniRef100: UniRef100_A0A024RAL6, UniRef100_D8L7E9, UniRef100_Q06413, UniRef100_A0A0D9SGI5
UniRef90: UniRef90_Q06413, UniRef90_F6WS85, UniRef90_Q8CFN5-4
UniRef50: UniRef50_Q8CFN5, UniRef50_Q06413, UniRef50_Q2KIA0
UniGene: Hs.649965
CCDS: CCDS54877.1, CCDS54878.1, CCDS87313.1, CCDS47245.1, CCDS47244.1, CCDS78034.1

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