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 131
Unique public DNA variants reported 45
Individuals with public variants 153
Hidden variants 0
Date created May 20, 2020
Date last updated May 20, 2020
Version FANCC:200520

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


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000073 9 Fanconi anemia, complementation group C, transcript variant 1 NM_000136.2 NP_000127.2 131
00000074 9 Fanconi anemia, complementation group C, transcript variant 2 NM_001243743.1 NP_001230672.1 131
00000075 9 Fanconi anemia, complementation group C, transcript variant 3 NM_001243744.1 NP_001230673.1 127


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