CLDN25 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
Aliases | CLDN25, claudin 25 | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | HomoloGene: 19476; GeneCards: CLDN25; OMA:CLDN25 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Claudin 25 is a protein that in humans is encoded by the CLDN25 gene. [3]
Function
[edit]This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. [provided by RefSeq, Jun 2010].
References
[edit]- ^ a b c GRCh38: Ensembl release 89: ENSG00000228607 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Entrez Gene: Claudin 25". Retrieved 2018-06-01.
- 1. ^ ª GRCh38: Ensembl release 89: ENSG00000228607 – Ensembl, May 2017
- 2. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- 3. ^ "Entrez Gene: Claudin 25". Retrieved 2018-06-01.
- 4. ^ Campbell M, Munnich A, Hashimoto Y (March 2024). “A loss of function mutation in CLDN25 causing Pelizaeus-Merzbacher-like leukodystrophy” Human Molecular Genetics, ddae038, PMID 38493358. DOI: 10.1093/hmg/ddae038. https://doi.org/10.1093/hmg/ddae038
Further reading
[edit]This article incorporates text from the United States National Library of Medicine, which is in the public domain.