Annexin A9

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Annexin A9 is a protein that in humans is encoded by the ANXA9 gene.[5][6][7]

Quick facts ANXA9, Identifiers ...
ANXA9
Identifiers
AliasesANXA9, ANX31, annexin A9
External IDsOMIM: 603319; MGI: 1923711; HomoloGene: 2643; GeneCards: ANXA9; OMA:ANXA9 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_003568

NM_001085383
NM_023628
NM_001379545
NM_001379546

RefSeq (protein)

NP_003559

NP_001078852
NP_076117
NP_001366474
NP_001366475

Location (UCSC)Chr 1: 150.98 – 151 MbChr 3: 95.2 – 95.21 Mb
PubMed search[3][4]
Wikidata
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Function

The annexins are a family of calcium-dependent phospholipid-binding proteins. Members of the annexin family contain 4 internal repeat domains, each of which includes a type II calcium-binding site. The calcium-binding sites are required for annexins to aggregate and cooperatively bind anionic phospholipids and extracellular matrix proteins. This gene encodes a divergent member of the annexin protein family in which all four homologous type II calcium-binding sites in the conserved tetrad core contain amino acid substitutions that ablate their function. However, structural analysis suggests that the conserved putative ion channel formed by the tetrad core is intact.[7]

References

Further reading

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