Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
8772
Gene name Gene Name - the full gene name approved by the HGNC.
Fas associated via death domain
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
FADD
Synonyms (NCBI Gene) Gene synonyms aliases
GIG3, IMD90, MORT1
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q13.3
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is an adaptor molecule that interacts with various cell surface receptors and mediates cell apoptotic signals. Through its C-terminal death domain, this protein can be recruited by TNFRSF6/Fas-receptor, tumor necrosis fact
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs369869993 T>C Likely-pathogenic Missense variant, coding sequence variant
rs387906839 T>G Pathogenic Missense variant, coding sequence variant
rs863224871 AGCGAGC>- Likely-pathogenic Stop gained, coding sequence variant
rs1392069885 G>A Likely-pathogenic Missense variant, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT000638 hsa-miR-146a-5p Luciferase reporter assay 19965651
MIRT006848 hsa-miR-155-5p GFP reporter assay, Immunohistochemistry, In situ hybridization, Luciferase reporter assay, Microarray, qRT-PCR, Western blot 21706480
MIRT006848 hsa-miR-155-5p GFP reporter assay, Immunohistochemistry, In situ hybridization, Luciferase reporter assay, Microarray, qRT-PCR, Western blot 21706480
MIRT023826 hsa-miR-1-3p Microarray 18668037
MIRT025869 hsa-miR-7-5p Sequencing 20371350
Transcription factors
Transcription factor Regulation Reference
DEDD Unknown 17193921
RUNX3 Activation 17956589
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001822 Process Kidney development IEA
GO:0001916 Process Positive regulation of T cell mediated cytotoxicity ISS
GO:0002020 Function Protease binding IPI 9208847, 21785459
GO:0002821 Process Positive regulation of adaptive immune response ISS
GO:0005123 Function Death receptor binding IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
602457 3573 ENSG00000168040
Protein
UniProt ID Q13158
Protein name FAS-associated death domain protein (FAS-associating death domain-containing protein) (Growth-inhibiting gene 3 protein) (Mediator of receptor induced toxicity)
Protein function Apoptotic adapter molecule that recruits caspases CASP8 or CASP10 to the activated FAS/CD95 or TNFRSF1A/TNFR-1 receptors (PubMed:16762833, PubMed:19118384, PubMed:20935634, PubMed:23955153, PubMed:24025841, PubMed:7538907, PubMed:9184224). The r
PDB 1A1W , 1A1Z , 1E3Y , 1E41 , 2GF5 , 3EZQ , 3OQ9 , 6ACI , 7LXC , 8YBX , 8YD7 , 8YD8 , 8YNI
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01335 DED 4 85 Death effector domain Domain
PF00531 Death 98 181 Death domain Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in a wide variety of tissues, except for peripheral blood mononuclear leukocytes. {ECO:0000269|PubMed:7538907}.
Sequence
Sequence length 208
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Platinum drug resistance
Apoptosis
Apoptosis - multiple species
Necroptosis
Toll-like receptor signaling pathway
NOD-like receptor signaling pathway
RIG-I-like receptor signaling pathway
Cytosolic DNA-sensing pathway
IL-17 signaling pathway
TNF signaling pathway
Alcoholic liver disease
Alzheimer disease
Pathways of neurodegeneration - multiple diseases
Pathogenic Escherichia coli infection
Salmonella infection
Chagas disease
Tuberculosis
Hepatitis C
Hepatitis B
Measles
Human cytomegalovirus infection
Influenza A
Human papillomavirus infection
Kaposi sarcoma-associated herpesvirus infection
Herpes simplex virus 1 infection
Epstein-Barr virus infection
Human immunodeficiency virus 1 infection
Pathways in cancer
  Caspase activation via Death Receptors in the presence of ligand
TRIF-mediated programmed cell death
Regulation by c-FLIP
RIPK1-mediated regulated necrosis
CASP8 activity is inhibited
TNFR1-induced proapoptotic signaling
Dimerization of procaspase-8
FasL/ CD95L signaling
TRAIL signaling
TLR3-mediated TICAM1-dependent programmed cell death
NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Epileptic encephalopathy Encephalopathies rs587776508, rs121918334, rs121918317, rs121918321, rs74315390, rs28939684, rs74315391, rs74315392, rs118192244, rs121918622, rs121918623, rs121917953, rs121917955, rs121918624, rs121918625
View all (860 more)
Hearing loss Sensorineural Hearing Loss (disorder), Sensory hearing loss rs267607135, rs267606855, rs779841884, rs267606854, rs28942097, rs121908073, rs121908076, rs74315289, rs121908144, rs111033313, rs74315437, rs121908348, rs121908349, rs121908350, rs397515359
View all (184 more)
17656375
Ventricular septal defect Ventricular Septal Defects rs104894073, rs387906775
Unknown
Disease term Disease name Evidence References Source
Coronary artery disease Coronary artery disease GWAS
Associations from Text Mining
Disease Name Relationship Type References
Adenocarcinoma of Lung Associate 16109772, 35029906
Aggressive Periodontitis Associate 28883894
Alzheimer Disease Associate 39396083
Aortic Dissection Associate 35480868
Arthritis Rheumatoid Associate 10817565
Arthritis Rheumatoid Inhibit 16951485
Autoimmune Lymphoproliferative Syndrome Associate 10200300, 33995372
Breast Neoplasms Associate 16450001, 18840411, 24886289, 27013580, 27388253, 31443698
Burkitt Lymphoma Associate 10477698, 21315423
Carcinogenesis Associate 27013580