Homo sapiens Protein: EDARADD
Summary
InnateDB Protein IDBP-107602.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol EDARADD
Protein Name EDAR-associated death domain
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000335076
InnateDB Gene IDBG-107598 (EDARADD)
Protein Structure
UniProt Annotation
Function Adapter protein that interacts with EDAR DEATH domain and couples the receptor to EDA signaling pathway during morphogenesis of ectodermal organs. Mediates the activation of NF- kappa-B. {ECO:0000269PubMed:11882293}.
Subcellular Localization Cytoplasm {ECO:0000305}.
Disease Associations Ectodermal dysplasia 11A, hypohidrotic/hair/nail type, autosomal dominant (ECTD11A) [MIM:614940]: A form of ectodermal dysplasia, a heterogeneous group of disorders due to abnormal development of two or more ectodermal structures. It is an autosomal dominant condition characterized by hypotrichosis, abnormal or missing teeth, and hypohidrosis due to the absence of sweat glands. {ECO:0000269PubMed:17354266, ECO:0000269PubMed:20979233}. Note=The disease is caused by mutations affecting the gene represented in this entry.Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive (ECTD11B) [MIM:614941]: A disorder due to abnormal development of two or more ectodermal structures, and characterized by sparse hair (atrichosis or hypotrichosis), abnormal or missing teeth and the inability to sweat due to the absence of sweat glands. {ECO:0000269PubMed:11780064, ECO:0000269PubMed:20222921}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Detected in adult pancreas, placenta and fetal skin, and at lower levels in lung, thymus, prostate and testis.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 9 experimentally validated interaction(s) in this database.
Experimentally validated
Total 9 [view]
Protein-Protein 9 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
Biological Process
GO:0001942 hair follicle development
GO:0007165 signal transduction
GO:0030154 cell differentiation
GO:0042475 odontogenesis of dentin-containing tooth
GO:0061153 trachea gland development
Cellular Component
GO:0005737 cytoplasm
Protein Structure and Domains
PDB ID
InterPro IPR000488 Death domain
IPR011029 Death-like domain
PFAM PF00531
PRINTS
PIRSF
SMART SM00005
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q8WWZ3
PhosphoSite PhosphoSite-Q8WWZ3
TrEMBL B1AL55
UniProt Splice Variant
Entrez Gene 128178
UniGene Hs.352224
RefSeq NP_665860
HUGO HGNC:14341
OMIM 606603
CCDS CCDS1610
HPRD 05965
IMGT
EMBL AK290862 AK291930 AK314634 AL136105 AL354693 AL450309 AY028906 AY028907 AY028908 AY028909 AY028910 AY028911 AY028912 AY028913 AY028914 AY071862 BC128082 CH471098
GenPept AAI28083 AAK40285 AAK40286 AAK40287 AAK40288 AAL60590 BAF83551 BAF84619 BAG37197 CAH70608 CAH70609 CAI22302 CAI22303 EAW70052