FANCM gene homepage

General information
Gene symbol FANCM
Gene name FA complementation group M
Chromosome 14
Chromosomal band q21.2
Imprinted Unknown
Genomic reference LRG_502
Transcript reference NM_020937.2
Associated with diseases POF15, SPGF28
Citation reference(s) -
Curators (1) Despoina Kalfakakou
Total number of public variants reported 309
Unique public DNA variants reported 131
Individuals with public variants 346
Hidden variants 0
Date created May 20, 2020
Date last updated September 23, 2020
Version FANCM:200923

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 23168
Entrez Gene 57697
PubMed articles FANCM
OMIM - Gene 609644
OMIM - Diseases POF15 (Premature ovarian failure 15)
SPGF28 (Spermatogenic failure 28)


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000085 14 Fanconi anemia, complementation group M NM_020937.2 NP_065988.1 309


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