Gene Gene information from NCBI Gene database.
Entrez ID 4674
Gene name Nucleosome assembly protein 1 like 2
Gene symbol NAP1L2
Synonyms (NCBI Gene)
BPX
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
miRNA miRNA information provided by mirtarbase database.
80
miRTarBase ID miRNA Experiments Reference
MIRT021545 hsa-miR-142-3p Microarray 17612493
MIRT440153 hsa-miR-369-3p HITS-CLIP 24374217
MIRT440153 hsa-miR-369-3p HITS-CLIP 24374217
MIRT1173655 hsa-miR-103b CLIP-seq
MIRT1173656 hsa-miR-2054 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
16
GO ID Ontology Definition Evidence Reference
GO:0000785 Component Chromatin IBA
GO:0003682 Function Chromatin binding IBA
GO:0003682 Function Chromatin binding IEA
GO:0005515 Function Protein binding IPI 18985028, 32296183, 32814053, 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
300026 7638 ENSG00000186462
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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

Accession ID Position in sequence Description Type
PF00956 NAP 110 411 Nucleosome assembly protein (NAP) Family
Sequence
Sequence length 460
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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
Abnormality of neuronal migration Uncertain significance ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MALFORMATIONS OF CORTICAL DEVELOPMENT, GROUP II Disgenet
★★☆☆☆
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
Acne Acne BEFREE 30909327
★☆☆☆☆
Found in Text Mining only
Acne Vulgaris Acne BEFREE 30909327
★☆☆☆☆
Found in Text Mining only
Colorectal Carcinoma Colorectal Cancer BEFREE 31397210
★☆☆☆☆
Found in Text Mining only
Dermatitis, Atopic Dermatitis BEFREE 26967585
★☆☆☆☆
Found in Text Mining only
Eczema Eczema BEFREE 26967585
★☆☆☆☆
Found in Text Mining only
Neural Tube Defects Neural Tube Defect BEFREE 12116227
★☆☆☆☆
Found in Text Mining only
Neurodegenerative Disorders Neurodegenerative Disorders BEFREE 25187168
★☆☆☆☆
Found in Text Mining only
Prostatic Neoplasms Prostatic neoplasm Pubtator 36195720 Associate
★☆☆☆☆
Found in Text Mining only