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Protein Coding Gene : Rmdn3 regulator of microtubule dynamics 3
Primary Identifier  MGI:1915059 Organism  mouse, laboratory
Chromosome  2 NCBI Gene Number  67809
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable microtubule binding activity. Predicted to be involved in intracellular calcium ion homeostasis. Predicted to act upstream of or within apoptotic process and cell differentiation. Located in mitochondrion. Is expressed in several structures, including eye. Orthologous to human RMDN3 (regulator of microtubule dynamics 3).
PHENOTYPE: Phenotypic analysis of mice homozygous for a gene trap allele indicates this mutation has no notable phenotype in any parameter tested. [provided by MGI curators]
  • synonyms:
  • RIKEN cDNA 1200015F23 gene,
  • 1200015F23Rik,
  • Rmdn3,
  • family with sequence similarity 82, member A2,
  • MGI:2138842,
  • AI131757,
  • Fam82a2,
  • expressed sequence AI131757,
  • regulator of microtubule dynamics 3
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Features --> Cross References

Genome

Sequence Feature Displayer

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0 Canonical

0 CDSs

0 Exons

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2 Involved In Mutations

Trail: ProteinCodingGene

0 Strain

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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

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Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

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