Gene Protein Transcript Blast result Transcript specific probe-cluster
Gene information for FANCM (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID57697
Official gene symbolFANCM
Full nameFanconi anemia, complementation group M
Gene summaryThe Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group M. [provided by RefSeq]
LocationChromosome: 14   Locus: 
Gene position45605136 - 45670093  Map Viewer
OMIM ID609644