The FADD gene homepage

General information
Gene symbol FADD
Gene name Fas (TNFRSF6)-associated via death domain
Chromosome 11
Chromosomal band q13.3
Imprinted Unknown
Genomic reference LRG_228
Transcript reference NM_003824.3
Associated with diseases dysplasia, otodental, chromsome deletion syndrome, Infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovascular malformations
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 8
Unique public DNA variants reported 6
Individuals with public variants 1
Hidden variants 1
Date created May 03, 2013
Date last updated September 17, 2021
Version FADD:210917

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 3573
Entrez Gene 8772
PubMed articles FADD
OMIM - Gene 602457
OMIM - Diseases Infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovascular malformations
Orphanet FADD

Active transcripts




NCBI ID     

NCBI Protein ID     

00007365 11 Fas (TNFRSF6)-associated via death domain NM_003824.3 NP_003815.1 8

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