NAP1L2
Nucleosome assembly protein 1-like 2
Also known as: BPX, MGC26243, NP1L2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9ULW6
- Gene
- NAP1L2
- Ensembl
- ENSG00000186462
- Chromosome
- X
- Canonical length
- 460 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Plasma membrane,Cytosol
OverviewNCBI Gene
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 RefSeq, Jan 2011]
Canonical amino-acid sequenceUniProt
460 residues, UniProt reviewed canonical sequence.
>Q9ULW6|NAP1L2
1 MAESENRKEL SESSQEEAGN QIMVEGLGEH LERGEDAAAG LGDDGKCGEE AAAGLGEEGE
61 NGEDTAAGSG EDGKKGGDTD EDSEADRPKG LIGYVLDTDF VESLPVKVKY RVLALKKLQT
121 RAANLESKFL REFHDIERKF AEMYQPLLEK RRQIINAIYE PTEEECEYKS DSEDCDDEEM
181 CHEEMYGNEE GMVHEYVDED DGYEDYYYDY AVEEEEEEEE EDDIEATGEE NKEEEDPKGI
241 PDFWLTVLKN VDTLTPLIKK YDEPILKLLT DIKVKLSDPG EPLSFTLEFH FKPNEYFKNE
301 LLTKTYVLKS KLAYYDPHPY RGTAIEYSTG CEIDWNEGKN VTLKTIKKKQ KHRIWGTIRT
361 VTEDFPKDSF FNFFSPHGIT SNGRDGNDDF LLGHNLRTYI IPRSVLFFSG DALESQQEGV
421 VREVNDAIYD KIIYDNWMAA IEEVKACCKN LEALVEDIDRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against NAP1L2 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.49
- Highest tissue expression
- 76 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 76 nTPM
- cerebellum: 71 nTPM
- hypothalamus: 41 nTPM
- hippocampal formation: 35 nTPM
- basal ganglia: 30 nTPM
- amygdala: 27 nTPM
Single-cell type
- brain excitatory neurons: 37 nCPM
- other brain neurons: 36 nCPM
- brain inhibitory neurons: 34 nCPM
- prostatic glandular cells: 30 nCPM
- retinal amacrine cells: 27 nCPM
- somatotrophs: 21 nCPM
Immune cell
- naive CD8 T-cell: 1.3 nTPM
- memory CD4 T-cell: 1.2 nTPM
- gdT-cell: 1 nTPM
- T-reg: 1 nTPM
- memory CD8 T-cell: 0.8 nTPM
- naive CD4 T-cell: 0.6 nTPM
Brain region
- cerebral cortex: 116 nTPM
- cerebellum: 70 nTPM
- hypothalamus: 69 nTPM
- white matter: 64 nTPM
- basal ganglia: 58 nTPM
- hippocampal formation: 57 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.51
- gnomAD pLI
- 0.78
- gnomAD missense Z
- 0.1
- DepMap mean gene effect
- 0.16
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- epigenetic regulation of gene expression
- neuron differentiation
- nucleosome assembly
- positive regulation of neuron differentiation
- regulation of stem cell division
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of NAP1L2 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
- H4
- SIRT1
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads NAP1L2 as an antibody target. Whether an autoantibody or antibody against NAP1L2 could matter depends on whether native NAP1L2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
NAP1L2 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label NAP1L2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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