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CLDN3 information


CLDN3
Identifiers
AliasesCLDN3, C7orf1, CPE-R2, CPETR2, HRVP1, RVP1, claudin 3
External IDsOMIM: 602910; MGI: 1329044; HomoloGene: 1001; GeneCards: CLDN3; OMA:CLDN3 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001306

NM_009902

RefSeq (protein)

NP_001297

NP_034032

Location (UCSC)Chr 7: 73.77 – 73.77 MbChr 5: 135.02 – 135.02 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Claudin 3, also known as CLDN3, is a protein which in humans is encoded by the CLDN3 gene.[5] It is a member of the claudin protein family.

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 intron-less gene, a member of the claudin family, is an integral membrane protein and a component of tight junction strands. It is also a low-affinity receptor for Clostridium perfringens enterotoxin, and shares amino acid sequence similarity with a putative apoptosis-related protein found in rat.[5]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000165215 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000070473 – 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. ^ a b "Entrez Gene: CLDN3 claudin 3".

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CLDN3

Last Update:

Claudin 3, also known as CLDN3, is a protein which in humans is encoded by the CLDN3 gene. It is a member of the claudin protein family. Tight junctions...

Word Count : 817

Williams syndrome

Last Update:

children without the syndrome. Williams syndrome genes ASL BAZ1B BCL7B CLDN3 CLDN4 CLIP2 EIF4H ELN FZD9 FKBP6 GTF2I GTF2IRD1 HIP1 KCTD7 LAT2 LIMK1 MDH2...

Word Count : 5772

Claudin

Last Update:

claudins their structural conservation are very similar. CLDN1, CLDN2, CLDN3, CLDN4, CLDN5, CLDN6, CLDN7, CLDN8, CLDN9, CLDN10, CLDN11, CLDN12, CLDN13...

Word Count : 1256

CLDN1

Last Update:

cholangitis syndrome. CLDN1 has been shown to interact with CLDN5 and CLDN3. GRCh38: Ensembl release 89: ENSG00000163347 – Ensembl, May 2017 GRCm38:...

Word Count : 946

CLDN5

Last Update:

velocardiofacial syndrome. CLDN5 has been shown to interact with CLDN1 and CLDN3. GRCh38: Ensembl release 89: ENSG00000184113 – Ensembl, May 2017 GRCm38:...

Word Count : 840

DNAJC30

Last Update:

BAZ1B (WSTF, WBSCR9), BCL7B, TBL2 (WS-βTRP), WBSCR14 (WS-bHLH), STX1A, CLDN3 (CPETR2, RVP1), CLDN4 (CPETR1), LIMK1, EIF4H (WBSCR1), WBSCR15 (WBSCR5)...

Word Count : 543

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