SMAD Family Member 4

Alternative Names

  • SMAD4
  • Mothers Against Decapentaplegic, Drosophila, Homolog of, 4
  • MADH4
  • SMA- and MAD-Related Protein 4
  • Deleted in Pancreatic Carcinoma 4
  • DPC4

Associated Diseases

Myhre Syndrome
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OMIM Number

600993

NCBI Gene ID

4089

Uniprot ID

Q13485

Length

54,830 bases

No. of Exons

12

No. of isoforms

1

Protein Name

Mothers against decapentaplegic homolog 4

Molecular Mass

60439 Da

Amino Acid Count

552

Genomic Location

chr18:51,030,212-51,085,041

Gene Map Locus
18q21.2

Description

This gene encodes a member of the Smad family of signal transduction proteins. Smad proteins are phosphorylated and activated by transmembrane serine-threonine receptor kinases in response to transforming growth factor (TGF)-beta signaling. The product of this gene forms homomeric complexes and heteromeric complexes with other activated Smad proteins, which then accumulate in the nucleus and regulate the transcription of target genes. This protein binds to DNA and recognizes an 8-bp palindromic sequence (GTCTAGAC) called the Smad-binding element (SBE). The protein acts as a tumor suppressor and inhibits epithelial cell proliferation. It may also have an inhibitory effect on tumors by reducing angiogenesis and increasng blood vessel hyperpermeability. The encoded protein is a crucial component of the bone morphogenetic protein signaling pathway. The Smad proteins are subject to complex regulation by post-translational modifications. Mutations or deletions in this gene have been shown to result in pancreatic cancer, juvenile polyposis syndrome, and hereditary hemorrhagic telangiectasia syndrome. [From RefSeq]

Epidemiology in the Arab World

View Map
Variant NameCountryGenomic LocationClinvar Clinical SignificanceCTGA Clinical Significance Condition(s)HGVS ExpressionsdbSNPClinvar
NM_005359.5:c.116_125delUnited Arab EmiratesNC_000018.10:g.51047162_51047171delLikely PathogenicMyhre SyndromeNG_013013.2:g.84123_84132del; NM_005359.5:c.116_125del; NP_005350.1:p.Ala39ValfsTer3
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