FTCDNL1 (formiminotransferase cyclodeaminase N-terminal like)

2014-11-01  

Identity

HGNC
LOCATION
2q33.1
LOCUSID
ALIAS
FONG

Other Information

Locus ID:

NCBI: 348751
MIM: 614308
HGNC: 48661
Ensembl: ENSG00000226124

Variants:

dbSNP: 348751
ClinVar: 348751
TCGA: ENSG00000226124
COSMIC: FTCDNL1

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000226124ENST00000416668H3BMM2
ENSG00000226124ENST00000420128H3BUS8
ENSG00000226124ENST00000420922H3BRX2
ENSG00000226124ENST00000622774E5RQL4

Expression (GTEx)

0
1
2
3
4
5

References

Pubmed IDYearTitleCitations
233033842013Association of the formiminotransferase N-terminal sub-domain containing gene and thrombospondin, type 1, domain-containing 7A gene with the prevalence of vertebral fracture in 2427 consecutive autopsy cases.1
215731282011Common variants in a novel gene, FONG on chromosome 2q33.1 confer risk of osteoporosis in Japanese.0
264924932015Association Study between the FTCDNL1 (FONG) and Susceptibility to Osteoporosis.0

Citation

Dessen P

FTCDNL1 (formiminotransferase cyclodeaminase N-terminal like)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/63616/ftcdnl1