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CLDN1

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Protein-coding gene in the species Homo sapiens
CLDN1
Identifiers
AliasesCLDN1, CLD1, ILVASC, SEMP1, claudin 1
External IDsOMIM: 603718; MGI: 1276109; HomoloGene: 9620; GeneCards: CLDN1; OMA:CLDN1 - orthologs
Gene location (Human)
Chromosome 3 (human)
Chr.Chromosome 3 (human)
Chromosome 3 (human)Genomic location for CLDN1Genomic location for CLDN1
Band3q28Start190,305,707 bp
End190,322,446 bp
Gene location (Mouse)
Chromosome 16 (mouse)
Chr.Chromosome 16 (mouse)
Chromosome 16 (mouse)Genomic location for CLDN1Genomic location for CLDN1
Band16|16 B2Start26,175,392 bp
End26,190,591 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • skin of thigh

  • germinal epithelium

  • skin of hip

  • skin of abdomen

  • olfactory zone of nasal mucosa

  • epithelium of nasopharynx

  • left uterine tube

  • right lobe of liver

  • nipple

  • gingival epithelium
Top expressed in
  • retinal pigment epithelium

  • decidua

  • molar

  • skin of external ear

  • lip

  • Epithelium of choroid plexus

  • epidermis

  • hair follicle

  • skin of abdomen

  • lumbar spinal ganglion
More reference expression data
BioGPS
More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

9076

12737

Ensembl

ENSG00000163347

ENSMUSG00000022512

UniProt

O95832

O88551

RefSeq (mRNA)

NM_021101

NM_016674

RefSeq (protein)

NP_066924

NP_057883

Location (UCSC)Chr 3: 190.31 – 190.32 MbChr 16: 26.18 – 26.19 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Claudin-1 is a protein that in humans is encoded by the CLDN1 gene. It belongs to the group of claudins.

Function

Tight junctions represent one mode of cell-to-cell adhesion in epithelial or endothelial cell sheets, forming continuous seals around cells and serving as a physical barrier to prevent solutes and water from passing freely through the paracellular space. These junctions are composed of sets of continuous networking strands in the outwardly facing cytoplasmic leaflet, with complementary grooves in the inwardly facing extracytoplasmic leaflet. The protein encoded by this gene, a member of the claudin family, is an integral membrane protein and a component of tight junction strands. Loss of function mutations result in neonatal ichthyosis-sclerosing cholangitis syndrome.

Interactions

CLDN1 has been shown to interact with CLDN5 and CLDN3.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000163347Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000022512Ensembl, 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. Halford S, Spencer P, Greenwood J, Winton H, Hunt DM, Adamson P (Jun 2000). "Assignment of claudin-1 (CLDN1) to human chromosome 3q28-->q29 with somatic cell hybrids". Cytogenet. Cell Genet. 88 (3–4): 217. doi:10.1159/000015553. PMID 10828592. S2CID 8896678.
  6. Morita K, Furuse M, Fujimoto K, Tsukita S (Mar 1999). "Claudin multigene family encoding four-transmembrane domain protein components of tight junction strands". Proc. Natl. Acad. Sci. U.S.A. 96 (2): 511–6. Bibcode:1999PNAS...96..511M. doi:10.1073/pnas.96.2.511. PMC 15167. PMID 9892664.
  7. "Entrez Gene: CLDN1 claudin 1".
  8. ^ Coyne CB, Gambling TM, Boucher RC, Carson JL, Johnson LG (Nov 2003). "Role of claudin interactions in airway tight junctional permeability". Am. J. Physiol. Lung Cell Mol. Physiol. 285 (5): L1166-78. doi:10.1152/ajplung.00182.2003. PMID 12909588.

External links

Further reading


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