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Immunogen sequence: MGYPEVERR ELLPAAAPRE RGSQGCGCGG APARAGEGNS CLLFLGFFGL SLALHLLTLC CYLELRSELR RERGAESRLG GSGTPGTSGT LSSLGGLDPD SPITSHLGQP SPKQQPLEPG EAALHSDSQD GHQ (1-132 aa encoded by BC126143)
EDA is a type II membrane protein that can be cleaved by furin to produce a secreted form. This protein, which belongs to the tumor necrosis factor family, acts as a homotrimer and may be involved in cell-cell signaling during the development of ectodermal organs. Defects in the gene for EDA are a cause of ectodermal dysplasia, anhidrotic, which is also known as X-linked hypohidrotic ectodermal dysplasia.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Ectodermal dysplasia protein; Ectodysplasin; Ectodysplasin-A; EDA 1; EDA protein; EDA protein homolog; oligodontia 1; Tabby protein; tumor necrosis factor ligand 7C; X-linked anhidroitic ectodermal dysplasia protein
Gene Aliases: ECTD1; ED1; ED1-A1; ED1-A2; EDA; EDA-A1; EDA-A2; EDA1; EDA2; HED; HED1; ODT1; STHAGX1; Ta; tabby; TNLG7C; XHED; XLHED
UniProt ID: (Human) Q92838, (Mouse) O54693
Entrez Gene ID: (Human) 1896, (Mouse) 13607
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