UMLS CUI | C0015625 |
UMLS Term | Fanconi Anemia |
MeSH ID | D005199 |
MeSH Term | Fanconi Anemia |
Disease Classes |
Hemic and Lymphatic Diseases Congenital, Hereditary, and Neonatal Diseases and Abnormalities Nutritional and Metabolic Diseases |
Gene Symbol | Description | Entrez ID | Uniprot ID | Chromosomal Location |
---|---|---|---|---|
ERCC4 |
excision repair cross-complementation group 4 |
2072 |
Q92889 |
chr16: 13,920,157-13,952,345 |
FANCD2 |
Fanconi anemia complementation group D2 |
2177 |
Q9BXW9 |
chr3: 10,026,414-10,101,930 |
FANCE |
Fanconi anemia complementation group E |
2178 |
Q9HB96 |
chr6: 35,452,361-35,467,103 |
FANCB |
Fanconi anemia complementation group B |
2187 |
Q8NB91 |
chrX: 14,843,407-14,873,069 |
FANCG |
Fanconi anemia complementation group G |
2189 |
O15287 |
chr9: 35,073,835-35,080,016 |
UBE2T |
ubiquitin conjugating enzyme E2T |
29089 |
Q9NPD8 |
chr1: 202,331,657-202,341,980 |
FANCI |
Fanconi anemia complementation group I |
55215 |
Q9NVI1 |
chr15: 89,243,949-89,317,261 |
FANCM |
Fanconi anemia complementation group M |
57697 |
Q8IYD8 |
chr14: 45,135,940-45,200,890 |
RAD51C |
RAD51 paralog C |
5889 |
O43502 |
chr17: 58,692,573-58,735,611 |
BRCA2 |
breast cancer 2 |
675 |
P51587 |
chr13: 32,315,474-32,400,266 |
TNF |
tumor necrosis factor |
7124 |
P01375 |
chr6: 31,575,567-31,578,336 |