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    Cldn19 claudin 19 [ Rattus norvegicus (Norway rat) ]

    Gene ID: 298487, updated on 9-Dec-2024

    Summary

    Official Symbol
    Cldn19provided by RGD
    Official Full Name
    claudin 19provided by RGD
    Primary source
    RGD:1305000
    See related
    EnsemblRapid:ENSRNOG00000007922 AllianceGenome:RGD:1305000
    Gene type
    protein coding
    RefSeq status
    PROVISIONAL
    Organism
    Rattus norvegicus
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Rattus
    Also known as
    claudin-19
    Summary
    Predicted to enable identical protein binding activity and paracellular tight junction channel activity. Predicted to be involved in several processes, including bicellular tight junction assembly; paracellular transport; and regulation of gene expression. Predicted to act upstream of or within apical junction assembly; neuronal action potential propagation; and tight junction organization. Predicted to be located in several cellular components, including apical junction complex; basolateral plasma membrane; and tight junction. Predicted to be active in bicellular tight junction and plasma membrane. Human ortholog(s) of this gene implicated in renal hypomagnesemia 5 with ocular involvement. Orthologous to human CLDN19 (claudin 19). [provided by Alliance of Genome Resources, Dec 2024]
    Expression
    Biased expression in Kidney (RPKM 62.4), Muscle (RPKM 16.5) and 5 other tissues See more
    Orthologs
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    Genomic context

    See Cldn19 in Genome Data Viewer
    Location:
    5q36
    Exon count:
    5
    Annotation release Status Assembly Chr Location
    RS_2024_02 current GRCr8 (GCF_036323735.1) 5 NC_086023.1 (138148234..138155672)
    RS_2023_06 previous assembly mRatBN7.2 (GCF_015227675.2) 5 NC_051340.1 (132862939..132870364)
    106 previous assembly Rnor_6.0 (GCF_000001895.5) 5 NC_005104.4 (138300692..138307982)

    Chromosome 5 - NC_086023.1Genomic Context describing neighboring genes Neighboring gene similar to human chromosome 1 open reading frame 50 Neighboring gene prolyl 3-hydroxylase 1 Neighboring gene Y box binding protein 1 Neighboring gene uncharacterized LOC134486981 Neighboring gene peptidylprolyl isomerase H

    Genomic regions, transcripts, and products

    Expression

    • Project title: A rat RNA-Seq transcriptomic BodyMap across 11 organs and 4 developmental stages
    • Description: 320 RNA samples isolated from 11 organs (adrenal gland, brain, heart, kidney, liver, lung, muscle, spleen, thymus, and testes or uterus) from both sexes of Fischer 344 rats across four developmental stages (2-, 6-, 21-, and 104-weeks-old)
    • BioProject: PRJNA238328
    • Publication: PMID 24510058
    • Analysis date: Mon Jun 6 17:44:12 2016

    Bibliography

    General gene information

    Gene Ontology Provided by RGD

    Function Evidence Code Pubs
    enables identical protein binding ISO
    Inferred from Sequence Orthology
    more info
     
    enables identical protein binding ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    enables paracellular tight junction channel activity ISO
    Inferred from Sequence Orthology
    more info
     
    enables paracellular tight junction channel activity ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    enables structural molecule activity IEA
    Inferred from Electronic Annotation
    more info
     
    Process Evidence Code Pubs
    involved_in actin cytoskeleton organization ISO
    Inferred from Sequence Orthology
    more info
     
    acts_upstream_of_or_within apical junction assembly ISO
    Inferred from Sequence Orthology
    more info
     
    involved_in bicellular tight junction assembly IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in cell adhesion IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in negative regulation of cell migration ISO
    Inferred from Sequence Orthology
    more info
     
    involved_in negative regulation of cell population proliferation ISO
    Inferred from Sequence Orthology
    more info
     
    involved_in negative regulation of gene expression ISO
    Inferred from Sequence Orthology
    more info
     
    involved_in negative regulation of wound healing ISO
    Inferred from Sequence Orthology
    more info
     
    acts_upstream_of_or_within neuronal action potential propagation ISO
    Inferred from Sequence Orthology
    more info
     
    involved_in paracellular transport ISO
    Inferred from Sequence Orthology
    more info
     
    involved_in paracellular transport ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in positive regulation of cell junction assembly ISO
    Inferred from Sequence Orthology
    more info
     
    involved_in positive regulation of gene expression ISO
    Inferred from Sequence Orthology
    more info
     
    involved_in positive regulation of protein phosphorylation ISO
    Inferred from Sequence Orthology
    more info
     
    involved_in regulation of transepithelial transport ISO
    Inferred from Sequence Orthology
    more info
     
    involved_in renal absorption ISO
    Inferred from Sequence Orthology
    more info
     
    involved_in renal absorption ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in retinal pigment epithelium development ISO
    Inferred from Sequence Orthology
    more info
     
    involved_in retinal pigment epithelium development ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    acts_upstream_of_or_within tight junction organization ISO
    Inferred from Sequence Orthology
    more info
     
    involved_in visual perception IEA
    Inferred from Electronic Annotation
    more info
     
    Component Evidence Code Pubs
    located_in Schmidt-Lanterman incisure IEA
    Inferred from Electronic Annotation
    more info
     
    located_in Schmidt-Lanterman incisure ISO
    Inferred from Sequence Orthology
    more info
     
    located_in apical junction complex ISO
    Inferred from Sequence Orthology
    more info
     
    located_in basolateral plasma membrane ISO
    Inferred from Sequence Orthology
    more info
     
    is_active_in bicellular tight junction IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in bicellular tight junction ISO
    Inferred from Sequence Orthology
    more info
     
    located_in cell junction ISO
    Inferred from Sequence Orthology
    more info
     
    located_in cytoplasm ISO
    Inferred from Sequence Orthology
    more info
     
    located_in mesaxon IEA
    Inferred from Electronic Annotation
    more info
     
    located_in mesaxon ISO
    Inferred from Sequence Orthology
    more info
     
    located_in nucleus ISO
    Inferred from Sequence Orthology
    more info
     
    located_in paranodal junction IEA
    Inferred from Electronic Annotation
    more info
     
    located_in paranodal junction ISO
    Inferred from Sequence Orthology
    more info
     
    located_in perinuclear region of cytoplasm ISO
    Inferred from Sequence Orthology
    more info
     
    is_active_in plasma membrane IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in plasma membrane ISO
    Inferred from Sequence Orthology
    more info
     
    located_in plasma membrane ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    located_in tight junction ISO
    Inferred from Sequence Orthology
    more info
     
    located_in tight junction ISS
    Inferred from Sequence or Structural Similarity
    more info
     

    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_001008514.1NP_001008514.1  claudin-19

      See identical proteins and their annotated locations for NP_001008514.1

      Status: PROVISIONAL

      Source sequence(s)
      BC079172
      UniProtKB/TrEMBL
      A6JZM5
      Related
      ENSRNOP00000099622.1, ENSRNOT00000128074.1
      Conserved Domains (1) summary
      cl21598
      Location:4182
      PMP22_Claudin; PMP-22/EMP/MP20/Claudin family

    RefSeqs of Annotated Genomes: GCF_036323735.1-RS_2024_02

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

    Reference GRCr8

    Genomic

    1. NC_086023.1 Reference GRCr8

      Range
      138148234..138155672
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_006238756.5XP_006238818.1  claudin-19 isoform X1

      See identical proteins and their annotated locations for XP_006238818.1

      UniProtKB/Swiss-Prot
      Q5QT56, Q6AY67
      UniProtKB/TrEMBL
      A6JZM4
      Related
      ENSRNOP00000050261.1, ENSRNOT00000047151.4
      Conserved Domains (1) summary
      cl21598
      Location:4182
      PMP22_Claudin; PMP-22/EMP/MP20/Claudin family