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Protein Coding Gene : Dctn5 dynactin 5

Primary Identifier  MGI:1891689 Organism  mouse, laboratory
Chromosome  7 NCBI Gene Number  59288
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Acts upstream of or within aorta development; coronary vasculature development; and ventricular septum development. Predicted to be located in centrosome; nuclear membrane; and nucleoplasm. Predicted to be part of dynactin complex. Is expressed in ganglia and metanephros. Orthologous to human DCTN5 (dynactin subunit 5).
PHENOTYPE: Mice homozygous for an ENU-induced mutation exhibit double outlet right ventricle (DORV), overriding aorta, and ventricular septal defect (VSD). Micrognathia, microcephaly/anencephaly and holoprosencephaly are also observed. [provided by MGI curators]
  • synonyms:
  • b2b315Clo,
  • expressed sequence C78178,
  • C78178,
  • RIKEN cDNA 4930427E12 gene,
  • Dctn5,
  • p25 dynactin subunit,
  • dynactin 5,
  • MGI:1914078,
  • MGI:5313699,
  • 4930427E12Rik,
  • Mutant line 315,
  • MGI:2142326

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

17 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