NASP (nuclear autoantigenic sperm protein)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 4678 |
| Gene name | Nuclear autoantigenic sperm protein |
| Gene symbol | NASP |
| Synonyms (NCBI Gene) |
FLB7527HMDRA1PRO1999
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| Chromosome | 1 |
| Chromosome location | 1p34.1 |
| Summary | This gene encodes a H1 histone binding protein that is involved in transporting histones into the nucleus of dividing cells. Multiple isoforms are encoded by transcript variants of this gene. The somatic form is expressed in all mitotic cells, is localize |
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miRNA
miRNA information provided by mirtarbase database.
90
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
21
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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P49321 | ||||||||||
| Protein name | Nuclear autoantigenic sperm protein (NASP) | ||||||||||
| Protein function | Component of the histone chaperone network (PubMed:22195965). Binds and stabilizes histone H3-H4 not bound to chromatin to maintain a soluble reservoir and modulate degradation by chaperone-mediated autophagy (PubMed:22195965). Required for DNA | ||||||||||
| PDB | 7V1K , 7V1L , 7V1M , 7V6P , 7V6Q | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Isoform 1 is testis- and sperm-specific. | ||||||||||
| Sequence |
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| Sequence length | 788 | ||||||||||
| Interactions | View interactions | ||||||||||
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
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Evidence Score:
★☆☆☆☆ Gene-disease association found in Text Mining only
★★☆☆☆ Found in Text Mining and Unknown/Other Associations
★★★☆☆ Reported in Unknown/Other Associations across ≥2 Sources
★★★★☆ ClinVar: Pathogenic/Likely Pathogenic (<5 Variants)
★★★★★ ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
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