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Cldn18 claudin 18 [ Mus musculus (house mouse) ]

Gene ID: 56492, updated on 2-Nov-2024

Summary

Official Symbol
Cldn18provided by MGI
Official Full Name
claudin 18provided by MGI
Primary source
MGI:MGI:1929209
See related
Ensembl:ENSMUSG00000032473 AllianceGenome:MGI:1929209
Gene type
protein coding
RefSeq status
REVIEWED
Organism
Mus musculus
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Mus; Mus
Summary
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. This gene is a downstream target gene regulated by the T/EBP/NKX2.1 homeodomain transcription factor. Four alternatively spliced transcript variants resulted from alternative promoters and alternative splicing have been identified, which encode two lung-specific isoforms and two stomach-specific isoforms respectively. This gene is also expressed in colons, inner ear and skin, and its expression is increased in both experimental colitis and ulcerative colitis. [provided by RefSeq, Aug 2010]
Expression
Biased expression in lung adult (RPKM 177.1), stomach adult (RPKM 118.5) and 1 other tissue See more
Orthologs
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Genomic context

See Cldn18 in Genome Data Viewer
Location:
9 E3.3; 9 52.0 cM
Exon count:
6
Annotation release Status Assembly Chr Location
RS_2024_02 current GRCm39 (GCF_000001635.27) 9 NC_000075.7 (99572849..99599320, complement)
108.20200622 previous assembly GRCm38.p6 (GCF_000001635.26) 9 NC_000075.6 (99690796..99717267, complement)

Chromosome 9 - NC_000075.7Genomic Context describing neighboring genes Neighboring gene alpha-1,4-N-acetylglucosaminyltransferase Neighboring gene DAZ interacting protein 1-like Neighboring gene STARR-seq mESC enhancer starr_25028 Neighboring gene predicted gene, 23949 Neighboring gene high mobility group box 1 pseudogene

Genomic regions, transcripts, and products

Expression

  • Project title: Mouse ENCODE transcriptome data Mouse ENCODE transcriptome data
  • Description: RNA profiling data sets generated by the Mouse ENCODE project.
  • BioProject: PRJNA66167
  • Publication: PMID 25409824
  • Analysis date: n/a

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Variation

Alleles

Alleles of this type are documented at Mouse Genome Informatics  (MGI)
  • Endonuclease-mediated (4) 
  • Targeted (7)  1 citation

General gene information

Gene Ontology Provided by MGI

Function Evidence Code Pubs
enables identical protein binding ISS
Inferred from Sequence or Structural Similarity
more info
 
enables protein binding IPI
Inferred from Physical Interaction
more info
PubMed 
enables structural molecule activity IEA
Inferred from Electronic Annotation
more info
 
Process Evidence Code Pubs
involved_in bicellular tight junction assembly IBA
Inferred from Biological aspect of Ancestor
more info
 
involved_in calcium-independent cell-cell adhesion via plasma membrane cell-adhesion molecules ISS
Inferred from Sequence or Structural Similarity
more info
 
involved_in cell adhesion IBA
Inferred from Biological aspect of Ancestor
more info
 
involved_in cellular response to estrogen stimulus IMP
Inferred from Mutant Phenotype
more info
PubMed 
acts_upstream_of_or_within digestive tract development IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in epithelial cell proliferation IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in epithelial fluid transport IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in lung alveolus development IMP
Inferred from Mutant Phenotype
more info
PubMed 
acts_upstream_of_or_within negative regulation of bone resorption IMP
Inferred from Mutant Phenotype
more info
PubMed 
acts_upstream_of_or_within negative regulation of osteoclast development IMP
Inferred from Mutant Phenotype
more info
PubMed 
acts_upstream_of_or_within negative regulation of protein localization to nucleus IDA
Inferred from Direct Assay
more info
PubMed 
involved_in negative regulation of protein localization to nucleus IMP
Inferred from Mutant Phenotype
more info
PubMed 
acts_upstream_of_or_within negative regulation of tumor necrosis factor-mediated signaling pathway IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in organ growth IMP
Inferred from Mutant Phenotype
more info
PubMed 
acts_upstream_of protein localization to nucleus IDA
Inferred from Direct Assay
more info
PubMed 
involved_in response to ethanol IEA
Inferred from Electronic Annotation
more info
 
involved_in tight junction assembly IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in tight junction organization IMP
Inferred from Mutant Phenotype
more info
PubMed 
Component Evidence Code Pubs
is_active_in bicellular tight junction IBA
Inferred from Biological aspect of Ancestor
more info
 
located_in bicellular tight junction ISS
Inferred from Sequence or Structural Similarity
more info
 
located_in cell-cell junction IDA
Inferred from Direct Assay
more info
PubMed 
located_in lateral plasma membrane IEA
Inferred from Electronic Annotation
more info
 
is_active_in plasma membrane IBA
Inferred from Biological aspect of Ancestor
more info
 
located_in plasma membrane IDA
Inferred from Direct Assay
more info
PubMed 
located_in tight junction IDA
Inferred from Direct Assay
more info
PubMed 

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

mRNA and Protein(s)

  1. NM_001194921.1NP_001181850.1  claudin-18 isoform A2.1

    See identical proteins and their annotated locations for NP_001181850.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (A2.1) is the stomach-specific form. It has an alternate 5' exon, as compared to variant A1.1. The resulting isoform (A2.1) is the same size but has a different N-terminus, as compared to isoform A1.1.
    Source sequence(s)
    AC157949, AF349451, AK033657
    Consensus CDS
    CCDS57694.1
    UniProtKB/TrEMBL
    Q8BZS5
    Related
    ENSMUSP00000108503.3, ENSMUST00000112882.9
    Conserved Domains (1) summary
    cl21598
    Location:9194
    PMP22_Claudin; PMP-22/EMP/MP20/Claudin family
  2. NM_001194922.1NP_001181851.1  claudin-18 isoform A1.2 precursor

    See identical proteins and their annotated locations for NP_001181851.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (A1.2) is the lung-specific form. It has an additional segment in the CDS, which results in an immediate translation termination, as compared to variant A1.1. The resulting isoform (A1.2) is C-terminal truncated, as compared to isoform A1.1.
    Source sequence(s)
    AC157949, AF349450, AK033657, BB663682
    Consensus CDS
    CCDS57692.1
    UniProtKB/Swiss-Prot
    P56857
    UniProtKB/TrEMBL
    Q8BZS5
    Related
    ENSMUSP00000115782.2, ENSMUST00000136429.8
    Conserved Domains (1) summary
    cl21598
    Location:43194
    PMP22_Claudin; PMP-22/EMP/MP20/Claudin family
  3. NM_001194923.1NP_001181852.1  claudin-18 isoform A2.2

    See identical proteins and their annotated locations for NP_001181852.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (A2.2) is the stomach-specific form. It has an alternate 5' exon, and an additional segment in the CDS, which results in an immediate translation termination, as compared to variant A1.1. The resulting isoform (A2.2) has a different N-terminus and is C-terminal truncated, as compared to isoform A1.1.
    Source sequence(s)
    AA028634, AC157949, AF349453
    Consensus CDS
    CCDS57693.1
    UniProtKB/Swiss-Prot
    P56857
    Related
    ENSMUSP00000117382.2, ENSMUST00000131922.2
    Conserved Domains (1) summary
    cl21598
    Location:9194
    PMP22_Claudin; PMP-22/EMP/MP20/Claudin family
  4. NM_019815.3NP_062789.1  claudin-18 isoform A1.1 precursor

    See identical proteins and their annotated locations for NP_062789.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (A1.1) is the lung-specific form. It encodes the longer isoform (A1.1).
    Source sequence(s)
    AC157949, AF221068, BB663682, BX528145, CF805431
    Consensus CDS
    CCDS23437.1
    UniProtKB/Swiss-Prot
    P56857, Q91ZY9, Q91ZZ0, Q91ZZ1
    UniProtKB/TrEMBL
    Q8BZS5
    Related
    ENSMUSP00000035048.6, ENSMUST00000035048.12
    Conserved Domains (1) summary
    cl21598
    Location:43194
    PMP22_Claudin; PMP-22/EMP/MP20/Claudin family

RefSeqs of Annotated Genomes: GCF_000001635.27-RS_2024_02

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCm39 C57BL/6J

Genomic

  1. NC_000075.7 Reference GRCm39 C57BL/6J

    Range
    99572849..99599320 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)