Disease Description

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