FANCC gene homepage - CanVaS - A Greek Cancer Patient Genetic Variation Resource

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CanVaS - A Greek Cancer Patient Genetic Variation Resource

FANCC (FA complementation group C)

LOVD v.3.0 Build 23 [ Current LOVD status ]
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	Curator: Despoina Kalfakakou

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FANCC gene homepage

General information
Gene symbol	FANCC
Gene name	FA complementation group C
Chromosome	9
Chromosomal band	q22.32
Imprinted	Unknown
Genomic reference	LRG_497
Transcript reference	NM_000136.2, NM_001243743.1, NM_001243744.1
Associated with diseases	FANCC
Citation reference(s)	-
Curators (1)	Despoina Kalfakakou
Total number of public variants reported	163
Unique public DNA variants reported	55
Individuals with public variants	188
Hidden variants	0
Date created	May 20, 2020
Date last updated	October 01, 2020
Version	FANCC:201001

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	3584
Entrez Gene	2176
PubMed articles	FANCC
OMIM - Gene	613899
OMIM - Diseases	FANCC (Fanconi anemia, complementation group C)

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
00000073	9	Fanconi anemia, complementation group C, transcript variant 1	NM_000136.2	NP_000127.2	163
00000074	9	Fanconi anemia, complementation group C, transcript variant 2	NM_001243743.1	NP_001230672.1	163
00000075	9	Fanconi anemia, complementation group C, transcript variant 3	NM_001243744.1	NP_001230673.1	157

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