ADAM9 ADAM metallopeptidase domain 9
Gene ID: 8754, updated on 12-Nov-2024Gene type: protein coding
Also known as: MCMP; MDC9; CORD9; Mltng
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- Go to complete Gene record for ADAM9
- Go to Variation Viewer for ADAM9 variants
Summary
This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The protein encoded by this gene interacts with SH3 domain-containing proteins, binds mitotic arrest deficient 2 beta protein, and is also involved in TPA-induced ectodomain shedding of membrane-anchored heparin-binding EGF-like growth factor. Several alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Jul 2010]
Associated conditions
See all available tests in GTR for this gene
Description | Tests |
---|---|
Cone-rod dystrophy 9 | See labs |
Genomic context
- Location:
- 8p11.22
- Sequence:
- Chromosome: 8; NC_000008.11 (38996973..39105261)
- Total number of exons:
- 24
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for ADAM9 variants |
Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ADAM9 @ LOVD
- 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
- Variation ViewerRelated Variants
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