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: 57697
MIM: 609644
HGNC: 23168
Ensembl: ENSG00000187790
Variants:
dbSNP: 57697
ClinVar: 57697
TCGA: ENSG00000187790
COSMIC: FANCM
RNA/Proteins
Expression (GTEx)
Pathways
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 35802266 | 2023 | Prevalence of FANCM germline variants in BRCA1/2 negative breast and/or ovarian cancer patients from Pakistan. | 0 |
| 36707629 | 2023 | FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women. | 2 |
| 35802266 | 2023 | Prevalence of FANCM germline variants in BRCA1/2 negative breast and/or ovarian cancer patients from Pakistan. | 0 |
| 36707629 | 2023 | FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women. | 2 |
| 34067580 | 2021 | A Genome-Wide Association Study for Hypertensive Kidney Disease in Korean Men. | 2 |
| 34067580 | 2021 | A Genome-Wide Association Study for Hypertensive Kidney Disease in Korean Men. | 2 |
| 32769987 | 2020 | DONSON and FANCM associate with different replisomes distinguished by replication timing and chromatin domain. | 21 |
| 33118316 | 2020 | FANCM c5791C>T stopgain mutation (rs144567652) is a familial colorectal cancer risk factor. | 6 |
| 32769987 | 2020 | DONSON and FANCM associate with different replisomes distinguished by replication timing and chromatin domain. | 21 |
| 33118316 | 2020 | FANCM c5791C>T stopgain mutation (rs144567652) is a familial colorectal cancer risk factor. | 6 |
| 29895858 | 2019 | A homozygous FANCM frameshift pathogenic variant causes male infertility. | 41 |
| 30426508 | 2019 | The identification of pathogenic variants in BRCA1/2 negative, high risk, hereditary breast and/or ovarian cancer patients: High frequency of FANCM pathogenic variants. | 32 |
| 30606611 | 2019 | Mammalian INO80 chromatin remodeler cooperates with FANCM to mediate DNA interstrand crosslink-induced checkpoint activation and repair. | 2 |
| 30714416 | 2019 | A tumor suppressive DNA translocase named FANCM. | 9 |
| 31067464 | 2019 | Remodeling of Interstrand Crosslink Proximal Replisomes Is Dependent on ATR, FANCM, and FANCD2. | 32 |
Citation
Dessen P
FANCM (FA complementation group M)
Atlas Genet Cytogenet Oncol Haematol. 2005-11-01
Online version: http://atlasgeneticsoncology.org/gene/43053/fancm-(fa-complementation-group-m)
