NAP1L3
| NAP1L3 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Identifiers | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Aliases | NAP1L3, MB20, NPL3, nucleosome assembly protein 1 like 3 | |||||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | OMIM: 300117; MGI: 1859565; GeneCards: NAP1L3 | |||||||||||||||||||||||||||||||||||||||||||||||||||||
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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.
 | This article on a gene on the human X chromosome and/or its associated protein is a stub. You can help Wikipedia by adding missing information. |
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