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Protein Coding Gene : Slc12a4 solute carrier family 12, member 4
Primary Identifier  MGI:1309465 Organism  mouse, laboratory
Chromosome  8 NCBI Gene Number  20498
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables potassium:chloride symporter activity. Involved in potassium ion transmembrane transport. Predicted to be located in membrane. Predicted to be active in plasma membrane. Is expressed in several structures, including adrenal gland; genitourinary system; nervous system; retina; and spleen. Orthologous to human SLC12A4 (solute carrier family 12 member 4).
PHENOTYPE: Mice homozygous for a constitutively active mutation display microcytosis and hypochromic anemia. [provided by MGI curators]
  • synonyms:
  • KCC1,
  • MGI:2142802,
  • K-Cl Co-transporter-1,
  • AW546649,
  • expressed sequence AW546649,
  • solute carrier family 12, member 4,
  • Slc12a4
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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

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Function

Mouse features --> Functions (GO terms)

Homology

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Interactions

4 Pathways

Trail: ProteinCodingGene

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Gene --> Protein-Protein Interactions

Expression

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Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

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