Type | Description |
---|---|
Definition | formimidoyltransferase cyclodeaminase |
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 |
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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Refseq |
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