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10841 FTCD

10841

FTCD

formimidoyltransferase cyclodeaminase

protein-coding

Homo sapiens

基因描述

Type Description
Definition formimidoyltransferase cyclodeaminase

研究结论

Date Results Publications
2020-11-21 13:22:00 The Diagnostic Value of Arginase-1, FTCD, and MOC-31 Expression in Early Detection of Hepatocellular Carcinoma (HCC) and in Differentiation Between HCC and Metastatic Adenocarcinoma to the Liver. 30784016
2019-05-04 10:19:00 the minor allele (A) of rs61735836 (p.Val101Met) in exon 3 of FTCD was associated with increased urinary Inorganic arsenics % (P = 8x10-13), increased mono-methylated arsenic % (P = 2x10-16) and decreased di-methylated arsenic % (P = 6x10-23). 30893314
2019-02-02 11:21:00 The rs914246 variant, but not the rs914245 variant, of the FTCD gene modulated accuracy in the task for younger, but not older, people under high working memory 29927301
2018-01-20 11:08:00 The formiminotransferase-cyclodeaminase allelic spectrum comprised of 12 distinct variants including 5 missense alterations, an in-frame deletion, two frameshift variants and four nonsense variants with the remaining alterations predicted to affect mRNA processing/stability. 29178637
2015-01-17 12:37:00 FTCD is a positive regulator of the hypoxia-HIF signaling pathway and has an important role in cell proliferation, metabolism and migration in HepG2 cells 24686083

名称对应

Type IDs
Synonymous LCHC1
Gene
UniProtKB-ID: FTCD_HUMAN
UniprotKB: O95954
UniParc: UPI000002A9F6, UPI000002A9F7, UPI000002A9F8, UPI000012AC75
EMBL: AF289021, AF169017, AF289022, U91541, AF289024, BC052248, AF289023, BC136383, BC136395
Ensembl: ENSG00000160282
KO: hsa:10841
Nucleutide sequences
EMBL-CDS: AAG01853.1, AAG01852.1, AAI36384.1, AAF15558.1, AAH52248.2, AAG01855.1, AAD15627.1, AAG01854.1, AAI36396.1
Ensembl_TRS: ENST00000291670, ENST00000397748, ENST00000397746
Protein sequencees
Ensembl_PRO: ENSP00000291670, ENSP00000380854, ENSP00000380856
RefSeq: XP_011527737.1, XP_011527739.1, NP_996848.1, NP_006648.1, XP_011527742.1, NP_001307341.1, XP_006724024.2, XP_011527741.1, XP_011527738.1, XP_006724025.2, XP_011527736.1
Others
UniRef100: UniRef100_O95954
UniRef90: UniRef90_O95954
UniRef50: UniRef50_O95954
UniGene: Hs.415846
CCDS: CCDS13731.1, CCDS82684.1

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