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NAP1L3





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

NAP1L3
Identifiers
AliasesNAP1L3, MB20, NPL3, nucleosome assembly protein 1 like 3
External IDsOMIM: 300117; MGI: 1859565; HomoloGene: 3334; GeneCards: NAP1L3; OMA:NAP1L3 - orthologs
Orthologs
SpeciesHumanMouse
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 MbChr X: 121.3 – 121.31 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Function

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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

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  1. ^ 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.

    • Further reading

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    This article incorporates text from the United States National Library of Medicine, which is in the public domain.


     

    This article on a gene on the human X chromosome and/or its associated protein is a stub. You can help Wikipedia by expanding it.

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    Last edited on 27 March 2022, at 09:05  





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