NAP1L1 Gene - Nucleosome Assembly Protein 1 Like 1

A comprehensive biomedical resource for NAP1L1, including gene card, expression, mutations, and disease associations.

Gene Information Card

Symbol NAP1L1
Full Name Nucleosome Assembly Protein 1 Like 1
Gene Type Protein coding
Chromosomal Location 12q21.1
NCBI Gene ID 4673 ncbi.nlm.nih.gov/gene/4673
Ensembl ID ENSG00000135446
UniProt ID P55209
OMIM ID 600982
HGNC ID 7637
Aliases NAP1, NAP1L, hNRP

Description

NAP1L1 (Nucleosome Assembly Protein 1 Like 1) is a protein-coding gene that encodes a member of the nucleosome assembly protein (NAP) family. This protein functions as a histone chaperone, facilitating the transport and deposition of histones H2A and H2B into nucleosomes, thereby playing a critical role in chromatin assembly, DNA replication, and transcriptional regulation. NAP1L1 is ubiquitously expressed and has been implicated in cell cycle progression and oncogenesis.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Colorectal Cancer Overexpression of NAP1L1 promotes cell proliferation and migration via chromatin remodeling and transcriptional activation of oncogenes. NCBI Gene, COSMIC
Hepatocellular Carcinoma Upregulation of NAP1L1 correlates with poor prognosis and enhanced tumor growth through histone chaperone activity. NCBI Gene, COSMIC
Breast Cancer NAP1L1 overexpression is associated with aggressive tumor phenotypes and may influence estrogen receptor signaling. NCBI Gene, COSMIC

Expression Profile

Tissue Expression
Tissue nTPM level
Testis 45.2 High
Bone Marrow 32.1 High
Lymph Node 28.7 High
Brain 15.3 Medium
Liver 12.8 Medium
Heart 8.4 Low
Cell Line Expression
Cell Line nTPM Notes
K562 (leukemia) 52.3 High expression
HeLa (cervical) 38.9 High expression
HepG2 (liver) 22.1 Medium expression
MCF7 (breast) 18.5 Medium expression
A549 (lung) 14.2 Medium expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.287A>G (p.Asn96Ser) Missense <0.01% Unknown; likely benign
c.544C>T (p.Arg182Trp) Missense <0.01% Unknown; reported in COSMIC
c.763_764insA (p.Thr255Asnfs*2) Frameshift <0.01% Loss of function; truncation
Mutation functional classification

Loss of Function (LOF)

Frameshift mutations (e.g., c.763_764insA) are predicted to cause loss of histone chaperone activity.

Gain of Function (GOF)

No gain-of-function mutations have been reported for NAP1L1.

Dominant Negative (DN)

No dominant-negative mutations have been characterized for NAP1L1.

Pathways

• Nucleosome assembly (REACT_1798)
• Chromatin modifying enzymes (REACT_1837)
• Cell cycle (REACT_152)

Protein Summary

The NAP1L1 protein (UniProt P55209) is a 391-amino acid histone chaperone that shuttles between the nucleus and cytoplasm. It binds specifically to histones H2A and H2B, facilitating their incorporation into nucleosomes during DNA replication and repair. NAP1L1 also interacts with importins and exportins to regulate its subcellular localization. The protein is highly conserved across eukaryotes and is essential for proper chromatin dynamics.

Related Products

Product name Cat.No. Species Gene ID
NAP1L1 Knockout HEK293 Cell Line EDJ-KQ50463 Human 4673 Details Get a Quote
NAP1L1 Knockout HeLa Cell Line EDJ-KQ53960 Human 4673 Details Get a Quote
NAP1L1 Knockout A-549 Cell Line EDJ-KQ62450 Human 4673 Details Get a Quote
NAP1L1 Knockout HCT 116 Cell Line EDJ-KQ70915 Human 4673 Details Get a Quote
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