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Protein Coding Gene : Gapdh glyceraldehyde-3-phosphate dehydrogenase

Primary Identifier  MGI:95640 Organism  mouse, laboratory
Chromosome  6 NCBI Gene Number  14433
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Enables enzyme binding activity and glyceraldehyde-3-phosphate dehydrogenase (NAD+) (phosphorylating) activity. Involved in canonical glycolysis; gluconeogenesis; and negative regulation of translation. Located in cytoplasm and plasma membrane. Part of GAIT complex. Is active in cytosol. Is expressed in several structures, including alimentary system; brain; early conceptus; genitourinary system; and sensory organ. Human ortholog(s) of this gene implicated in Alzheimer's disease. Orthologous to human GAPDH (glyceraldehyde-3-phosphate dehydrogenase).
PHENOTYPE: Mutant heterozygotes show reduced enzyme levels. The currently known mutant allels are homozygous lethal. [provided by MGI curators]
  • synonyms:
  • Gapdh,
  • MGD-MRK-9967,
  • AK190093,
  • Gapd,
  • cDNA sequence AK190093,
  • MGI:3579984,
  • glyceraldehyde-3-phosphate dehydrogenase

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

5 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

 

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0 Driver For