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Protein Coding Gene : Slc16a7 solute carrier family 16 (monocarboxylic acid transporters), member 7

Primary Identifier  MGI:1330284 Organism  mouse, laboratory
Chromosome  10 NCBI Gene Number  20503
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables symporter activity. Predicted to be involved in plasma membrane lactate transport and pyruvate transmembrane transport. Predicted to be located in cytosol and nucleoplasm. Predicted to be active in several cellular components, including Schaffer collateral - CA1 synapse; basolateral plasma membrane; and hippocampal mossy fiber to CA3 synapse. Is expressed in several structures, including alimentary system; early conceptus; genitourinary system; integumental system; and nervous system. Orthologous to human SLC16A7 (solute carrier family 16 member 7).
  • synonyms:
  • RIKEN cDNA 9030411M13 gene,
  • MGI:1918785,
  • AI428890,
  • MGI:2143596,
  • RIKEN cDNA 4921534N07 gene,
  • solute carrier family 16 (monocarboxylic acid transporters), member 7,
  • MGI:2444072,
  • RIKEN cDNA D630004K10 gene,
  • 9030411M13Rik,
  • D630004K10Rik,
  • Slc16a7,
  • 4921534N07Rik,
  • MCT2,
  • expressed sequence AI428890

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

4 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

Other

0 Driver For