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Labor Staber Humangenetik

FA complementation group M (FANCM)

LOVD v.3.0 Build 16 [ Current LOVD status ]
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Curator: Florian Bayersdorfer

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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	BREAST CANCER
Citation reference(s)	-
Curators (1)	Florian Bayersdorfer
Total number of public variants reported	1
Unique public DNA variants reported	1
Individuals with public variants	0
Hidden variants	0
Date created	December 07, 2018
Date last updated	December 07, 2018
Version	FANCM:181207

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	BREAST CANCER (BREAST CANCER, FAMILIAL)
HGMD	FANCM
GeneCards	FANCM
GeneTests	FANCM

Active transcripts

Legend

Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.

ID	Chr	Name	NCBI ID	NCBI Protein ID	Variants
00000041	14	Fanconi anemia, complementation group M	NM_020937.2	NP_065988.1	1

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