NAP1L2 (nucleosome assembly protein 1 like 2)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 4674 |
| Gene name | Nucleosome assembly protein 1 like 2 |
| Gene symbol | NAP1L2 |
| Synonyms (NCBI Gene) |
BPX
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| Chromosome | X |
| Chromosome location | Xq13.2 |
| Summary | The protein encoded by this intronless gene is a member of the nucleosome assembly protein (NAP) family. The encoded protein represents a class of tissue-specific factors that interact with chromatin to regulate neuronal cell proliferation. [provided by R |
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miRNA
miRNA information provided by mirtarbase database.
80
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
16
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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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Q9ULW6 | ||||||||||
| Protein name | Nucleosome assembly protein 1-like 2 (Brain-specific protein, X-linked) | ||||||||||
| Protein function | Acidic protein which may be involved in interactions with other proteins or DNA. | ||||||||||
| Family and domains |
Pfam
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| Sequence |
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| Sequence length | 460 | ||||||||||
| Interactions | View interactions | ||||||||||
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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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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