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Protein Coding Gene : Cldn12 claudin 12

Primary Identifier  MGI:1929288 Organism  mouse, laboratory
Chromosome  5 NCBI Gene Number  64945
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Predicted to enable identical protein binding activity. Predicted to be involved in calcium-independent cell-cell adhesion via plasma membrane cell-adhesion molecules. Located in lateral plasma membrane and tight junction. Is expressed in several structures, including alimentary system; brain; cardiovascular system; genitourinary system; and integumental system. Orthologous to human CLDN12 (claudin 12).
PHENOTYPE: Homozygotes for a knock-out allele show no signs of blood-brain barrier tight junction dysfunction under healthy or neuroinflammatory conditions. However, subtle and mostly sex specific alterations associated with CNS, energy metabolism, and cardiovascular functions are observed. [provided by MGI curators]
  • synonyms:
  • claudin 12,
  • Cldn12

Features --> Cross References

Genome

Sequence Feature Displayer

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0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

0 Involved In Mutations

0 Strain

0 Transcripts

0 Transgenic Expressors

0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

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Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

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0 Driver For