APOLD1 apolipoprotein L domain containing 1
Gene ID: 81575, updated on 18-Sep-2024Gene type: protein coding
Also known as: BDVAS; VERGE
- See all available tests in GTR for this gene
- Go to complete Gene record for APOLD1
- Go to Variation Viewer for APOLD1 variants
Summary
APOLD1 is an endothelial cell early response protein that may play a role in regulation of endothelial cell signaling and vascular function (Regard et al., 2004 [PubMed 15102925]).[supplied by OMIM, Dec 2008]
Associated conditions
See all available tests in GTR for this gene
Description | Tests |
---|---|
Bleeding disorder, vascular-type | not available |
Genomic context
- Location:
- 12p13.1
- Sequence:
- Chromosome: 12; NC_000012.12 (12725917..12791466)
- Total number of exons:
- 3
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for APOLD1 variants |
Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- MedGenRelated information in MedGen
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- Variation ViewerRelated Variants
IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.