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10 sources retrieved · Most recent: April 2026 · Index updated 15 days ago
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AKAP17A
A-kinase anchoring protein 17A
Chromosome X|Y · X;Y
NCBI Gene: 8227Ensembl: ENSG00000197976.13HGNC: HGNC:18783UniProt: Q02040
66PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
nucleusRNA bindingprotein bindingprotein kinase A bindingAbnormality of prenatal development or birthovarian carcinomaulcerative colitiscancer
✦AI Summary

AKAP17A (A-kinase anchoring protein 17A) is a multifunctional RNA-binding protein that plays critical roles in mRNA processing and cellular signaling. Its primary function involves regulating alternative splicing and mRNA processing through multiple mechanisms 1. AKAP17A serves as a key component of the SOS splicing system, binding to transposable element (TE)-containing mRNAs and facilitating their excision from host transcripts through interaction with RNA ligase RTCB and bridging protein CAAP1 23. This spliceosome-independent mechanism protects genes from DNA transposon-mediated disruption by recognizing inverted terminal repeat patterns. Additionally, AKAP17A promotes hypoxic adaptation by augmenting HIF1α protein synthesis through a PKA-independent pathway, supporting tumor growth and cellular oxygen homeostasis 4. The protein also interacts with CAAP1 in mRNA splicing pathways, influencing platinum sensitivity in ovarian cancer 5. AKAP17A expression levels are associated with aging phenotypes, particularly cognitive decline and physical ability deterioration 1. In sex chromosome X|Y, AKAP17A shows altered expression patterns that correlate with X chromosome X|Y, suggesting its involvement in epigenetic regulation 67. Clinical significance includes potential biomarker applications in cancer drug resistance and aging-related cognitive decline.

Sources cited
1
AKAP17A binds TE-containing mRNAs and is required for SOS splicing system with RTCB and CAAP1
PMID: 41372403
2
AKAP17A transcript levels are associated with cognitive decline and aging phenotypes
PMID: 31292793
3
AKAP17A participates in spliceosome-independent SOS splicing to excise DNA transposons from mRNAs
PMID: 40027818
4
AKAP17A interacts with CAAP1 in mRNA splicing pathways and correlates with platinum sensitivity in ovarian cancer
PMID: 36870674
5
AKAP17A promotes HIF1α protein synthesis and supports hypoxic adaptation and tumor growth
PMID: 41391802
6
AKAP17A shows altered expression patterns in sex chromosome aneuploidies across multiple tissues
PMID: 36978128
7
AKAP17A is differentially expressed in Turner and Klinefelter syndromes and involved in gene expression regulation
PMID: 32959501
Disease Associationsⓘ20
Abnormality of prenatal development or birthOpen Targets
0.10Suggestive
ovarian carcinomaOpen Targets
0.01Suggestive
ulcerative colitisOpen Targets
0.01Suggestive
cancerOpen Targets
0.01Suggestive
bladder transitional cell carcinomaOpen Targets
0.01Suggestive
lung adenocarcinomaOpen Targets
0.01Suggestive
obsessive-compulsive disorderOpen Targets
0.01Suggestive
prostate adenocarcinomaOpen Targets
0.01Suggestive
Tourette syndromeOpen Targets
0.01Suggestive
neoplasmOpen Targets
0.01Suggestive
AutoimmunityOpen Targets
0.01Suggestive
diffuse large B-cell lymphomaOpen Targets
0.00Suggestive
chronic lymphocytic leukemiaOpen Targets
0.00Suggestive
lymphomaOpen Targets
0.00Suggestive
chronic obstructive pulmonary diseaseOpen Targets
0.00Suggestive
esophageal adenocarcinomaOpen Targets
0.00Suggestive
gastric adenocarcinomaOpen Targets
0.00Suggestive
lymphoproliferative syndromeOpen Targets
0.00Suggestive
readingOpen Targets
0.00Suggestive
respiratory distress syndrome in premature infantsOpen Targets
0.00Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
ASMTProtein interaction79%ASMTLProtein interaction78%SLC25A6Protein interaction75%CAAP1Protein interaction59%RBM12BShared pathway50%AHNAK2Shared pathway50%
Tissue Expression6 tissues
Ovary
100%
Liver
93%
Bone Marrow
79%
Lung
74%
Heart
18%
Brain
11%
Gene Interaction Network
Click a node to explore
AKAP17AASMTASMTLSLC25A6CAAP1RBM12BAHNAK2
PROTEIN STRUCTURE
Preparing viewer…
AlphaFoldAI-predicted · UniProt Q02040
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
0.44Moderately Constrained
pLIⓘ
1.00Intolerant
Observed/Expected LoF0.29 [0.19–0.44]
RankingsWhere AKAP17A stands among ~20K protein-coding genes
  • #7,038of 20,598
    Most Researched66
  • #2,427of 17,882
    Most Constrained (LOEUF)0.44 · top quartile
Genes detectedAKAP17A
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
An RNA splicing system that excises DNA transposons from animal mRNAs.
PMID: 41372403
Nature · 2026
1.00
2
The transcript expression levels of HNRNPM, HNRNPA0 and AKAP17A splicing factors may be predictively associated with ageing phenotypes in human peripheral blood.
PMID: 31292793
Biogerontology · 2019
0.90
3
An RNA Splicing System that Excises Transposons from Animal mRNAs.
PMID: 40027818
bioRxiv · 2025
0.80
4
Proteomic analysis reveals CAAP1 negatively correlates with platinum resistance in ovarian cancer.
PMID: 36870674
J Proteomics · 2023
0.70
5
Host Genetic and Gut Microbial Signatures in Familial Inflammatory Bowel Disease.
PMID: 32764209
Clin Transl Gastroenterol · 2020
0.60