LOVD FANCG homepage

General information
Gene name Fanconi anemia, complementation group G
Gene symbol FANCG
Chromosome Location 9p13
Database location https://research.cchmc.org/LOVD2/
Curator Ammar Husami
PubMed references View all (unique) PubMed references in the FANCG database
Date of creation May 01, 2014
Last update May 01, 2014
Version FANCG140501
Add sequence variant Submit a sequence variant
First time submitters Register here
Reference sequence file Genomic reference sequence for describing sequence variants
Exon/intron information Exon/intron information table
Total number of unique DNA variants reported 0
Total number of individuals with variant(s) 0
Total number of variants reported 0
Subscribe to updates of this gene

Graphical displays and utilities
Summary tables Summary of all sequence variants in the FANCG database, sorted by type of variant (with graphical displays and statistics)
Reading-frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes
UCSC Genome Browser Show variants in the UCSC Genome Browser (compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 3588
Entrez Gene 2189
OMIM - Gene 602956
UniProtKB (SwissProt/TrEMBL) O15287