NAP1L3
NAP1L3 | |||||||||||||||||||||||||
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Identifiers | |||||||||||||||||||||||||
Aliases | NAP1L3, MB20, NPL3, nucleosome assembly protein 1 like 3 | ||||||||||||||||||||||||
External IDs | OMIM: 300117 MGI: 1859565 HomoloGene: 3334 GeneCards: NAP1L3 | ||||||||||||||||||||||||
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Orthologs | |||||||||||||||||||||||||
Species | Human | Mouse | |||||||||||||||||||||||
Entrez | |||||||||||||||||||||||||
Ensembl | |||||||||||||||||||||||||
UniProt | |||||||||||||||||||||||||
RefSeq (mRNA) | |||||||||||||||||||||||||
RefSeq (protein) | |||||||||||||||||||||||||
Location (UCSC) | Chr X: 93.67 – 93.67 Mb | Chr X: 121.3 – 121.31 Mb | |||||||||||||||||||||||
PubMed search | [3] | [4] | |||||||||||||||||||||||
Wikidata | |||||||||||||||||||||||||
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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[]
- ^ 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[]
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
Categories:
- Genes on human chromosome X
- Human chromosome X gene stubs