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EDA (gene)

EDA
Protein EDA PDB 1rj7.png
Available structures
PDB Human UniProt search: PDBe RCSB
Identifiers
Aliases EDA, ECTD1, ED1, ED1-A1, ED1-A2, EDA-A1, EDA-A2, EDA1, EDA2, HED, HED1, ODT1, STHAGX1, XHED, XLHED, TNLG7C, ectodysplasin A
External IDs GeneCards: EDA
Gene location (Human)
X chromosome (human)
Chr. X chromosome (human)
X chromosome (human)
Genomic location for EDA
Genomic location for EDA
Band Xq13.1 Start 69,616,067 bp
End 70,039,469 bp
RNA expression pattern
PBB GE EDA 206217 at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

n/a

RefSeq (protein)

NP_001005609
NP_001005610
NP_001005612
NP_001005613
NP_001390

n/a

Location (UCSC) Chr X: 69.62 – 70.04 Mb n/a
PubMed search n/a

1RJ7, 1RJ8

NM_001005614
NM_001399

n/a

NP_001005609
NP_001005610
NP_001005612
NP_001005613
NP_001390

n/a

Ectodysplasin A (EDA) is a protein that in humans is encoded by the EDA gene.

Ectodysplasin A is a transmembrane protein of the TNF family which plays an important role in the development of ectodermal tissues such as skin in humans. It is recognized by the ectodysplasin A receptor.

The protein encoded by this gene is a type II membrane protein that can be cleaved by furin to produce a secreted form. The encoded 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. Along with c-Met, it has been shown to be involved in the differentiation of anatomical placodes, precursors of scales, feathers and hair follicles in vertebrates. Defects in this gene are a cause of ectodermal dysplasia, anhidrotic, which is also known as X-linked hypohidrotic ectodermal dysplasia. Several transcript variants encoding many different isoforms have been found for this gene.


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Wikipedia

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