APOL3

Chr 22

apolipoprotein L3

Also known as: APOLIII, CG121, CG12_1, apoL-III

This gene is a member of the apolipoprotein L gene family, and it is present in a cluster with other family members on chromosome 22. The encoded protein is found in the cytoplasm, where it may affect the movement of lipids, including cholesterol, and/or allow the binding of lipids to organelles. In addition, expression of this gene is up-regulated by tumor necrosis factor-alpha in endothelial cells lining the normal and atherosclerotic iliac artery and aorta. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2015]

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ClinVar variants
0
Pathogenic / LP
pLI score
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Active trials
Clinical SummaryAPOL3
Some data sources returned errors (2)

gnomad: Error: gnomAD API error: 502

clinvarCount: Error: NCBI fetch failed: 429 https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esearch.fcgi

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

0 submitted variants in ClinVar

Protein Context — Lollipop Plot

APOL3 · protein map & ClinVar variants

Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.

OMIM — Genotype-Phenotype Relationships

1 OMIM entry

APOLIPOPROTEIN L3; APOL3
MIM #607253 · *
Clinical Literature
Landmark / reviewRecent case evidence
Key Publications
Landmark & review papers · by relevance
PubMed
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Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

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