The FANCC gene homepage

General information
Gene symbol FANCC
Gene name FA complementation group C
Chromosome 9
Chromosomal band q22.32
Imprinted Unknown
Genomic reference NG_011707.1
Transcript reference NM_000136.2
Associated with diseases -
Citation reference(s) -
Refseq URL Coding DNA reference sequence
Curators (1) Instituto Nacional del Cancer
Total number of public variants reported 15
Unique public DNA variants reported 11
Individuals with public variants 15
Hidden variants -
Date created December 31, 1969
Date last updated December 31, 1969
Version FANCC:691231

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
Homepage URL https://www.ncbi.nlm.nih.gov/nuccore/NM_000136.2
HGNC 3584
Entrez Gene 2176
PubMed articles FANCC
OMIM - Gene 613899


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000045 9 Fanconi anemia complementation group C, transcript variant 1 NM_000136.2 NP_000127.2 15


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