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Gene : ADAM9 Homo sapiens

Name  ? ADAM metallopeptidase domain 9 Cytological Location  8p11.22
Brief Description  ADAM metallopeptidase domain 9
description  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]
  • synonyms:
  • MDC9,
  • MCMP,
  • KIAA0021,
  • HGNC:216,
  • cone rod dystrophy 9,
  • Mltng,
  • a disintegrin and metalloproteinase domain 9 (meltrin gamma),
  • CORD9,
  • NM_003816,
  • MDC9,
  • MCMP,
  • uc003xmr.4,
  • U41766,
  • ADAM9,
  • Mltng,
  • CORD9,
  • meltrin gamma,
  • OTTHUMG00000159783
  • identifiers:
  • 8754,
  • ENSG00000168615,
  • ADAM9

Genome feature

Region: gene ? Length: 108495  
Location: 8:38996767-39105261 Cyto location: 8p11.22


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Function

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Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

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Interactions

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Expression

Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.

 

Other

620 SN Ps

5 Cross References

17 Data Sets

29 Homologues

0 Located Features

90 Rna Seq Results