Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 348751
MIM: 614308
HGNC: 48661
Ensembl: ENSG00000226124
Variants:
dbSNP: 348751
ClinVar: 348751
TCGA: ENSG00000226124
COSMIC: FTCDNL1
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000226124 | ENST00000416668 | H3BMM2 |
| ENSG00000226124 | ENST00000420128 | H3BUS8 |
| ENSG00000226124 | ENST00000420922 | H3BRX2 |
| ENSG00000226124 | ENST00000622774 | E5RQL4 |
Expression (GTEx)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 26492493 | 2015 | Association Study between the FTCDNL1 (FONG) and Susceptibility to Osteoporosis. | 4 |
| 26492493 | 2015 | Association Study between the FTCDNL1 (FONG) and Susceptibility to Osteoporosis. | 4 |
| 23303384 | 2013 | Association 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. | 2 |
| 23303384 | 2013 | Association 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. | 2 |
| 21573128 | 2011 | Common variants in a novel gene, FONG on chromosome 2q33.1 confer risk of osteoporosis in Japanese. | 15 |
| 21573128 | 2011 | Common variants in a novel gene, FONG on chromosome 2q33.1 confer risk of osteoporosis in Japanese. | 15 |
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-(formiminotransferase-cyclodeaminase-n-terminal-like)
