AKAP7
A-kinase anchor protein 7 isoform gamma
Also known as: AKA7G_HUMAN, AKAP15, AKAP18
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9P0M2
- Gene
- AKAP7
- Ensembl
- ENSG00000118507
- Chromosome
- 6
- Canonical length
- 348 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Vesicles
OverviewNCBI Gene
This gene encodes a member of the A-kinase anchoring protein (AKAP) family, a group of functionally related proteins that bind to a regulatory subunit (RII) of cAMP-dependent protein kinase A (PKA) and target the enzyme to specific subcellular compartments. AKAPs have a common RII-binding domain, but contain different targeting motifs responsible for directing PKA to distinct intracellular locations. Three alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq, Apr 2011]
Canonical amino-acid sequenceUniProt
348 residues, UniProt reviewed canonical sequence.
>Q9P0M2|AKAP7
1 MERPEAGGIN SNECENVSRK KKMSEEFEAN TMDSLVDMPF ATVDIQDDCG ITDEPQINLK
61 RSQENEWVKS DQVKKRKKKR KDYQPNYFLS IPITNKEIIK GIKILQNAII QQDERLAKAM
121 VSDGSFHITL LVMQLLNEDE VNIGIDALLE LKPFIEELLQ GKHLTLPFQG IGTFGNQVGF
181 VKLAEGDHVN SLLEIAETAN RTFQEKGILV GESRSFKPHL TFMKLSKSPW LRKNGVKKID
241 PDLYEKFISH RFGEEILYRI DLCSMLKKKQ SNGYYHCESS IVIGEKNGGE PDDAELVRLS
301 KRLVENAVLK AVQQYLEETQ NKNKPGEGSS VKTEAADQNG NDNENNRKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against AKAP7 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.4
- Highest tissue expression
- 54 nTPM
Expression across tissuesHPA
Tissue
- adrenal gland: 54 nTPM
- pancreas: 39 nTPM
- duodenum: 28 nTPM
- liver: 23 nTPM
- colon: 18 nTPM
- rectum: 18 nTPM
Single-cell type
- bergmann glia: 320 nCPM
- adrenal cortex cells: 273 nCPM
- cholangiocytes: 245 nCPM
- pancreatic duct cells: 220 nCPM
- oligodendrocyte progenitor cells: 168 nCPM
- sertoli cells: 137 nCPM
Immune cell
- naive CD4 T-cell: 18 nTPM
- basophil: 17 nTPM
- MAIT T-cell: 13 nTPM
- memory CD4 T-cell: 12 nTPM
- memory CD8 T-cell: 11 nTPM
- naive CD8 T-cell: 11 nTPM
Brain region
- cerebellum: 22 nTPM
- spinal cord: 21 nTPM
- cerebral cortex: 20 nTPM
- hypothalamus: 20 nTPM
- midbrain: 20 nTPM
- basal ganglia: 18 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.22
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.17
- DepMap mean gene effect
- 0.03
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
- nucleotide binding
- protein kinase A binding
- protein kinase A regulatory subunit binding
- protein kinase binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of AKAP7 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads AKAP7 as an antibody target. Whether an autoantibody or antibody against AKAP7 could matter depends on whether native AKAP7 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
AKAP7 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label AKAP7 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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