SMAD4 SMAD family member 4
Gene ID: 4089, updated on 12-Nov-2024Gene type: protein coding
Also known as: JIP; DPC4; MADH4; MYHRS
- See all available tests in GTR for this gene
- Go to complete Gene record for SMAD4
- Go to Variation Viewer for SMAD4 variants
Summary
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 increasing 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. [provided by RefSeq, May 2022]
Associated conditions
See all available tests in GTR for this gene
Description | Tests |
---|---|
A genome-wide association study of host genetic determinants of the antibody response to Anthrax Vaccine Adsorbed. GeneReviews: Not available | |
Carcinoma of pancreas MedGen: C0235974GeneReviews: Not available | not available |
Juvenile polyposis syndrome | not available |
Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome MedGen: C1832942OMIM: 175050GeneReviews: Hereditary Hemorrhagic Telangiectasia, Juvenile Polyposis Syndrome | not available |
Myhre syndrome | not available |
Copy number response
Description |
---|
Copy number response Triplosensitivity No evidence available (Last evaluated 2020-12-16) ClinGen Genome Curation PageHaploinsufficency Sufficient evidence for dosage pathogenicity (Last evaluated 2020-12-16) ClinGen Genome Curation PagePubMed |
Genomic context
- Location:
- 18q21.2
- Sequence:
- Chromosome: 18; NC_000018.10 (51030213..51085042)
- Total number of exons:
- 14
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for SMAD4 variants |
Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- MedGenRelated information in MedGen
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- RefSeqGeneLink to Nucleotide RefSeqGenes
- SMAD4 Database
- SMAD4 database
- Variation ViewerRelated Variants
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