NAP1L3

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

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)[1] Band Xq21.32 Start 93,670,930 bp[1] End 93,673,578 bp[1]
Gene location (Mouse) Chr. X chromosome (mouse)[2] Band X|X E3 Start 121,304,262 bp[2] End 121,307,098 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) 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 BioGPS n/a
Orthologs Species Human Mouse Entrez 4675 54561 Ensembl ENSG00000186310 ENSMUSG00000055733 UniProt Q99457 Q794H2 RefSeq (mRNA) NM_004538 NM_138742 RefSeq (protein) NP_004529 NP_620081 Location (UCSC) Chr X: 93.67 – 93.67 Mb Chr X: 121.3 – 121.31 Mb PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

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].