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5019 OXCT1

5019

OXCT1

3-oxoacid CoA-transferase 1

protein-coding

Homo sapiens

基因描述

Type Description
Definition 3-oxoacid CoA-transferase 1

研究结论

Date Results Publications
2014-07-19 12:59:00 Crystal structure of human SCOT, providing a molecular understanding of the reported mutations based on their potential structural effects. 23420214
2014-04-12 10:34:00 Case Report: Succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency causes episodic ketoacidotic crises and no apparent symptoms between them. 20652411
2012-02-11 10:29:00 Data show that the ketone body metabolizing enzymes BDH1, BDH2, OXCT1 and ACAT1 were expressed at the mRNA and protein level in all glioma cell lines. 21791085
2011-05-21 11:23:00 Missense Mutations in succinyl-CoA:3-ketoacid CoA transferase is associated with Ketoacidosis. 21296660
2010-12-05 22:08:00 Observational study of gene-disease association. (HuGE Navigator) 20877624

名称对应

Type IDs
Synonymous OXCT, SCOT
Gene
UniProtKB-ID: SCOT1_HUMAN, A0A024R040_HUMAN
UniprotKB: P55809, A0A024R040
UniParc: UPI0000000C9A, UPI0001914DFB
EMBL: CH471119, AC008817, AK312327, AB029576, GQ900952, BC009001, U62961, AK298352, AC034222, AC114946, AK315902
Ensembl: ENSG00000083720
KO: hsa:5019
Nucleutide sequences
EMBL-CDS: AAB07366.1, BAH14273.1, AAH09001.1, BAB13733.1, BAG35249.1, BAH12764.1, ADO22469.1, EAW56015.1, EAW56014.1
Gene_ORFName: hCG_37537
Ensembl_TRS: ENST00000512084, ENST00000196371, ENST00000510634
Protein sequencees
Ensembl_PRO: ENSP00000421143, ENSP00000423144, ENSP00000196371
RefSeq: NP_001351229.1, NP_001351228.1, NP_001351230.1, NP_001351231.1, NP_001351232.1, NP_000427.1
Others
UniRef100: UniRef100_P55809
UniRef90: UniRef90_P55809
UniRef50: UniRef50_P55809
UniGene: Hs.278277
CCDS: CCDS3937.1

全选

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