NAP1L1 nucleosome assembly protein 1 like 1
Gene ID: 4673, updated on 5-Mar-2024Gene type: protein coding
Also known as: NRP; NAP1; NAP1L
- See all available tests in GTR for this gene
- Go to complete Gene record for NAP1L1
- Go to Variation Viewer for NAP1L1 variants
Summary
This gene encodes a member of the nucleosome assembly protein (NAP) family. This protein participates in DNA replication and may play a role in modulating chromatin formation and contribute to the regulation of cell proliferation. Alternative splicing results in multiple transcript variants encoding different isoforms; however, not all have been fully described. [provided by RefSeq, Apr 2015]
Associated conditions
See all available tests in GTR for this gene
Description | Tests |
---|---|
Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. GeneReviews: Not available |
Genomic context
- Location:
- 12q21.2
- Sequence:
- Chromosome: 12; NC_000012.12 (76036585..76084685, complement)
- Total number of exons:
- 16
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | GeneView ReportGo to Variation Viewer for NAP1L1 variants |
1000 Genomes | See 1000 Genomes Browser (GRCh37.p13) |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- SNP: GeneViewSNPs linked from GeneView
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