FASLG homepage - CCHMC Molecular Genetics Laboratory Mutation Database

General information
Gene name	Fas ligand (TNF superfamily, member 6)
Gene symbol	FASLG
Chromosome Location	1q23
Database location	https://research.cchmc.org/LOVD2/
Curator	Ammar Husami
PubMed references	View all (unique) PubMed references in the FASLG database
Date of creation	April 30, 2010
Last update	April 30, 2010
Version	FASLG100430
Add sequence variant	Submit a sequence variant
First time submitters	Register here
Reference sequence file	coding DNA reference sequence for describing sequence variants
Genomic refseq ID	NG_007269.1
Transcript refseq ID	NM_000639.1
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
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Graphical displays and utilities
Summary tables	Summary of all sequence variants in the FASLG 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	11936
Entrez Gene	356
OMIM - Gene	134638
UniProtKB (SwissProt/TrEMBL)	P48023
HGMD	FASLG
GeneCards	FASLG
GeneTests	FASLG
External link	Mutation registry for Autoimmune lymphoproliferative syndrome, type 1B (ALPS1B)

CCHMC Molecular Genetics Laboratory Mutation Database