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Protein Coding Gene : Vdac1 voltage-dependent anion channel 1

Primary Identifier  MGI:106919 Organism  mouse, laboratory
Chromosome  11 NCBI Gene Number  22333
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0)

Enables oxysterol binding activity and voltage-gated monoatomic anion channel activity. Involved in negative regulation of reactive oxygen species metabolic process and regulation of mitophagy. Acts upstream of or within behavioral fear response; learning; and neuron-neuron synaptic transmission. Located in membrane and mitochondrion. Is expressed in several structures, including central nervous system; eye; liver; placenta; and testis. Human ortholog(s) of this gene implicated in prostate cancer. Orthologous to human VDAC1 (voltage dependent anion channel 1).
PHENOTYPE: Homozygous null mutants exhibit approximately 60% embryonic mortality, with loss occurring at embryonic day 10.5-11.5. Survivors exhibit defective cued fear conditioning and spatial learning. Heterozygotes also exhibit about 12% prenatal mortality. [provided by MGI curators]
  • synonyms:
  • AL033343,
  • expressed sequence AL033343,
  • MGI:2144363,
  • voltage-dependent anion channel 1,
  • MGD-MRK-35380,
  • Vdac1,
  • Vdac5

Features --> Cross References

Genome

Sequence Feature Displayer

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0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

1 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

12 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