Gene
NOS1AP
nitric oxide synthase 1 adaptor protein
- HGNC 16859↗(opens in a new tab)
- Ensembl gene ENSG00000198929↗(opens in a new tab)
- NCBI Gene 9722↗(opens in a new tab)
Summary
- Cytogenetic location
- 1q23.3
- Coordinates
- Chromosome 1: 162,069,691–162,370,475 (GRCh38)
- Exons
- 10 exons across 300.8 kb
- Protein
- 506 amino acids
- Also known as
- KIAA0464, CAPON
- MANE Select transcript
- ENST00000361897.10NM_014697.3
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Nephrotic Syndrome
- Nephrosis
Pathological processes of the KIDNEY without inflammatory or neoplastic components. Nephrosis may be a primary disorder or secondary complication of other diseases. It is characterized by the NEPHROTIC SYNDROME indicating the presence of PROTEINURIA and HYPOALBUMINEMIA with accompanying EDEMA.
- 1 GenCC submitter rates it definitive or strong
How NOS1AP is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Stretches short reads find hard
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 5 kb of the gene's 300.8 kb; 1,521 of those bases code for the protein.
Genes linked to the same conditions
- ACTN4actinin alpha 4Shares 1 condition
- ARHGDIARho GDP dissociation inhibitor alphaShares 1 condition
- COQ6coenzyme Q6, monooxygenaseShares 1 condition
- COQ8Bcoenzyme Q8BShares 1 condition
- DAAM2dishevelled associated activator of morphogenesis 2Shares 1 condition
- DGKEdiacylglycerol kinase epsilonShares 1 condition
- DLC1DLC1 Rho GTPase activating proteinShares 1 condition
- EMP2epithelial membrane protein 2Shares 1 condition
- ITSN1intersectin 1Shares 1 condition
- ITSN2intersectin 2Shares 1 condition
- KANK2KN motif and ankyrin repeat domains 2Shares 1 condition
- LAMA5laminin subunit alpha 5Shares 1 condition
Traits linked to NOS1AP
The Human Phenotype Ontology lists these as features of the rare conditions NOS1AP can cause. Each trait's page lists the other genes linked to it.
External links
Gene records
Transcript
Protein
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
- GenCC and ClinGen, released 2026-10-16: which conditions the gene is linked to, and how strongly.
- The ACMG secondary findings list, SF v3.2.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). NOS1AP gene: nitric oxide synthase 1 adaptor protein. Retrieved 17 October 2026, from https://dantelabs.com/genes/nos1ap
Dante Labs. NOS1AP gene: nitric oxide synthase 1 adaptor protein [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/nos1ap
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