AKAP11

Human protein-coding gene From Wikipedia, the free encyclopedia

A-kinase anchor protein 11 is an enzyme that in humans is encoded by the AKAP11 gene.[5][6][7]

AliasesAKAP11, AKAP-11, AKAP220, PPP1R44, PRKA11, A-kinase anchoring protein 11
End42,323,261 bp[1]
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AKAP11
Identifiers
AliasesAKAP11, AKAP-11, AKAP220, PPP1R44, PRKA11, A-kinase anchoring protein 11
External IDsOMIM: 604696; MGI: 2684060; HomoloGene: 8279; GeneCards: AKAP11; OMA:AKAP11 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_016248
NM_144490

NM_001164503
NM_001346784

RefSeq (protein)

NP_057332

n/a

Location (UCSC)Chr 13: 42.27 – 42.32 MbChr 14: 78.73 – 78.77 Mb
PubMed search[3][4]
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Function

The A-kinase anchor proteins (AKAPs) are a group of structurally diverse proteins, which have the common function of binding to the regulatory subunit of protein kinase A (PKA) and confining the holoenzyme to discrete locations within the cell. This gene encodes a member of the AKAP family. The encoded protein is expressed at high levels throughout spermatogenesis and in mature sperm. It binds the RI and RII subunits of PKA in testis. It may serve a function in cell cycle control of both somatic cells and germ cells in addition to its putative role in spermatogenesis and sperm function.[7]

Interactions

AKAP11 has been shown to interact with:

Role in bipolar disorder

AKAP11 has been identified as a definitive risk gene for bipolar disorder based on a whole-exome study of 13933 patients with bipolar disorder matched with 14422 controls.[14]

References

Further reading

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