Lipase family member N is a protein that in humans is encoded by the LIPN gene. [5]

Function

The gene encodes a lipase that is highly expressed in granular keratinocytes in the epidermis, and plays a role in the differentiation of keratinocytes. Mutations in this gene are associated with lamellar ichthyosis type 4. [provided by RefSeq, Dec 2011].

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000204020 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000024770 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "Entrez Gene: Lipase family member N". Retrieved 2019-12-02.

Further reading


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

Allikas: http://en.wikipedia.org/wiki/LIPN_(gene)
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