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10 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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ANKAR
ankyrin and armadillo repeat containing
Chromosome 2 · 2q32.2
NCBI Gene: 150709Ensembl: ENSG00000151687.15HGNC: HGNC:26350UniProt: Q70AK8
10PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
✓ Swiss-Prot Reviewed
membraneovarian neoplasmAbnormal nasolacrimal system morphologyglomerulonephritishead and neck malignant neoplasia
✦AI Summary

ANKAR (ankyrin and armadillo repeat containing) is a protein-coding gene located on chromosome 2 that encodes a molecule containing ankyrin and armadillo repeat domains. Limited functional characterization is available in the provided literature. ANKAR was identified as a circulating extracellular vesicle (EV) protein associated with metastatic pancreatic ductal adenocarcinoma (PDAC) in a large-scale proteomics study of 124 individuals 1. Specifically, EVs with elevated ANKAR levels, alongside PSMB4 and RUVBL2, correlated with metastatic disease in PDAC patients 1. This suggests ANKAR may play a role in cancer progression or metastasis, though the molecular mechanisms remain unclear. ANKAR was also identified as one of 21 genes affected by a hemizygous 3.4 Mb deletion on chromosome 2.1-q32.3 in an aortic dissection patient, but haploinsufficiency of ANKAR was not demonstrated as causative for the observed phenotype 2. The protein's structural features—containing ankyrin and armadillo repeats—suggest potential roles in protein-protein interactions and cellular signaling, but direct functional studies are needed. Current evidence limits ANKAR to potential involvement in cancer metastasis, though clinical significance remains to be established.

Sources cited
1
ANKAR was identified as an extracellular vesicle protein associated with metastatic pancreatic cancer in a large proteomics analysis of 124 individuals
PMID: 39693144
2
ANKAR was identified as one of 21 genes affected by a hemizygous deletion on chromosome 2q32.1-q32.3 in an aortic dissection patient, but haploinsufficiency was not demonstrated
PMID: 20648054
⚠Limited data available — This gene has 2 indexed publications. Summary and analysis may be incomplete.
Disease Associationsⓘ20
ovarian neoplasmOpen Targets
0.26Weak
Abnormal nasolacrimal system morphologyOpen Targets
0.25Weak
glomerulonephritisOpen Targets
0.03Suggestive
head and neck malignant neoplasiaOpen Targets
0.03Suggestive
Lung AbscessOpen Targets
0.02Suggestive
bronchopneumoniaOpen Targets
0.02Suggestive
hypertrophic cardiomyopathyOpen Targets
0.02Suggestive
diabetes mellitusOpen Targets
0.02Suggestive
placenta praeviaOpen Targets
0.02Suggestive
medical procedureOpen Targets
0.02Suggestive
osteoarthritis, hipOpen Targets
0.02Suggestive
metastatic neoplasmOpen Targets
0.00Suggestive
endometrial cancerOpen Targets
0.00Suggestive
hemochromatosis type 4Open Targets
0.00Suggestive
acute myeloid leukemiaOpen Targets
0.00Suggestive
colorectal adenocarcinomaOpen Targets
0.00Suggestive
lung cancerOpen Targets
0.00Suggestive
ThymomaOpen Targets
0.00Suggestive
Uterine CarcinosarcomaOpen Targets
0.00Suggestive
uterine corpus endometrial carcinomaOpen Targets
0.00Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
OSGEPL1Protein interaction93%TMF1Protein interaction82%
Tissue Expression6 tissues
Ovary
100%
Heart
51%
Bone Marrow
50%
Lung
42%
Liver
38%
Brain
24%
Gene Interaction Network
Click a node to explore
ANKAROSGEPL1TMF1
PROTEIN STRUCTURE
Preparing viewer…
AlphaFoldAI-predicted · UniProt Q70AK8
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
1.07LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF0.91 [0.78–1.07]
RankingsWhere ANKAR stands among ~20K protein-coding genes
  • #16,981of 20,598
    Most Researched10
  • #10,811of 17,882
    Most Constrained (LOEUF)1.07
Genes detectedANKAR
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
A large-scale proteomics resource of circulating extracellular vesicles for biomarker discovery in pancreatic cancer.
PMID: 39693144
Elife · 2024
1.00
2
Effect of Empagliflozin on the Mechanisms Driving Erythropoiesis and Iron Mobilization in Patients With Heart Failure: The EMPEROR Program.
PMID: 40335252
J Am Coll Cardiol · 2025
0.90
3
Hemizygous deletion of COL3A1, COL5A2, and MSTN causes a complex phenotype with aortic dissection: a lesson for and from true haploinsufficiency.
PMID: 20648054
Eur J Hum Genet · 2010
0.80
4
Bartholin gland cyst: a clinical image.
PMID: 36879636
Pan Afr Med J · 2022
0.70
5
Combined Systemic Immunotherapy and Intrathecal Dexamethasone in Febrile Infection Related Epilepsy Syndrome.
PMID: 39932904
Ann Clin Transl Neurol · 2025
0.60