Gene Gene information from NCBI Gene database.
Entrez ID 4676
Gene name Nucleosome assembly protein 1 like 4
Gene symbol NAP1L4
Synonyms (NCBI Gene)
NAP1L4bNAP2NAP2LhNAP2
Chromosome 11
Chromosome location 11p15.4
Summary This gene encodes a member of the nucleosome assembly protein (NAP) family which can interact with both core and linker histones. It can shuttle between the cytoplasm and nucleus, suggesting a role as a histone chaperone. This gene is one of several locat
miRNA miRNA information provided by mirtarbase database.
283
miRTarBase ID miRNA Experiments Reference
MIRT048253 hsa-miR-196a-5p CLASH 23622248
MIRT692017 hsa-miR-3120-3p HITS-CLIP 23313552
MIRT692016 hsa-miR-512-5p HITS-CLIP 23313552
MIRT692015 hsa-miR-10b-3p HITS-CLIP 23313552
MIRT692014 hsa-miR-922 HITS-CLIP 23313552
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
17
GO ID Ontology Definition Evidence Reference
GO:0000785 Component Chromatin IBA
GO:0003682 Function Chromatin binding IBA
GO:0003723 Function RNA binding HDA 22658674
GO:0005515 Function Protein binding IPI 22190034, 24981860, 28514442, 33961781
GO:0005634 Component Nucleus IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
601651 7640 ENSG00000205531
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q99733
Protein name Nucleosome assembly protein 1-like 4 (Nucleosome assembly protein 2) (NAP-2)
Protein function Acts as a histone chaperone in nucleosome assembly.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00956 NAP 65 338 Nucleosome assembly protein (NAP) Family
Tissue specificity TISSUE SPECIFICITY: Ubiquitous. Biallelically expressed in fetal and adult tissues. Highest levels in testis. {ECO:0000269|PubMed:8923002}.
Sequence
Sequence length 375
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
GOUT GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Neoplasms Neoplasms BEFREE 9325046
★☆☆☆☆
Found in Text Mining only
Nephroblastoma Nephroblastoma BEFREE 9325046
★☆☆☆☆
Found in Text Mining only