U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Links from GEO Profiles

    • Showing Current items.

    Cldn18 claudin 18 [ Mus musculus (house mouse) ]

    Gene ID: 56492, updated on 27-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
    NEW
    Try the new Gene table
    Try the new Transcript table

    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
    • 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)

    NEW Try the new Transcript table

    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)