NAP1L3

NAP1L3
Identifiers
Aliases	NAP1L3, MB20, NPL3, nucleosome assembly protein 1 like 3
External IDs	OMIM: 300117; MGI: 1859565; HomoloGene: 3334; GeneCards: NAP1L3; OMA:NAP1L3 - orthologs
Gene location (Human)
Chr.	X chromosome (human)
End	93,673,578 bp
Gene location (Mouse)
Chr.	X chromosome (mouse)
End	121,307,098 bp
RNA expression pattern
	Top expressed in
	Brodmann area 23; ; lateral nuclear group of thalamus; ; superior vestibular nucleus; ; pons; ; endothelial cell; ; pars compacta; ; superior frontal gyrus; ; parietal lobe; ; postcentral gyrus; ; cerebellar vermis;
	Top expressed in
	dorsomedial hypothalamic nucleus; ; ventral tegmental area; ; dorsal tegmental nucleus; ; medial vestibular nucleus; ; lateral hypothalamus; ; superior colliculus; ; habenula; ; paraventricular nucleus of hypothalamus; ; central gray substance of midbrain; ; pontine nuclei;
	More reference expression data
	n/a
Orthologs
	4675
	54561
	ENSG00000186310
	ENSMUSG00000055733
	Q99457
	Q794H2
	NM_004538
	NM_138742
	NP_004529
	NP_620081
	Wikidata
View/Edit Human	View/Edit Mouse

Nucleosome assembly protein 1 like 3 is a protein that in humans is encoded by the NAP1L3 gene.^[5]

Function

This gene is intronless and encodes a member of the nucleosome assembly protein (NAP) family. This gene is linked closely to a region of genes responsible for several X-linked cognitive disability syndromes. [provided by RefSeq, Dec 2010].

References

1 2 3 GRCh38: Ensembl release 89: ENSG00000186310 – Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000055733 – Ensembl, May 2017
↑ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
↑ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
↑ "Entrez Gene: Nucleosome assembly protein 1 like 3". Retrieved 2018-05-22.

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NAP1L3

Function

References

Further reading