NAP1L3

NAP1L3
Identifiers
Aliases	NAP1L3, MB20, NPL3, nucleosome assembly protein 1 like 3
External IDs	OMIM: 300117 MGI: 1859565 HomoloGene: 3334 GeneCards: NAP1L3
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; ; superior vestibular nucleus; ; pons; ; endothelial cell; ; superior frontal gyrus; ; parietal lobe; ; postcentral gyrus; ; cerebellar vermis; ; occipital lobe; ; orbitofrontal cortex;
	Top expressed in
	dorsomedial hypothalamic nucleus; ; ventral tegmental area; ; dorsal tegmental nucleus; ; medial vestibular nucleus; ; lateral hypothalamus; ; superior colliculus; ; habenula; ; paraventricular nucleus of hypothalamus; ; pontine nuclei; ; barrel cortex;
	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 edit

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 edit

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000186310 – Ensembl, May 2017
^ ^a ^b ^c 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.

NAP1L3

Function edit

References edit

Further reading edit