FANCF gene homepage

General information
Gene symbol FANCF
Gene name FA complementation group F
Chromosome 11
Chromosomal band p14.3
Imprinted Unknown
Genomic reference LRG_527
Transcript reference NM_022725.3
Associated with diseases FANCF
Citation reference(s) -
Curators (1) Despoina Kalfakakou
Total number of public variants reported 102
Unique public DNA variants reported 28
Individuals with public variants 107
Hidden variants 0
Date created May 20, 2020
Date last updated October 07, 2020
Version FANCF:201007

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 3587
Entrez Gene 2188
PubMed articles FANCF
OMIM - Gene 613897
OMIM - Diseases FANCF (Fanconi anemia, complementation group F)


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000079 11 Fanconi anemia, complementation group F NM_022725.3 NP_073562.1 102


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