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Protein Coding Gene : Efhd1 EF hand domain containing 1

Primary Identifier  MGI:1921607 Organism  mouse, laboratory
Chromosome  1 NCBI Gene Number  98363
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0)

Predicted to enable calcium ion sensor activity. Acts upstream of or within neuron projection development. Located in mitochondrial inner membrane. Is expressed in adrenal gland; cochlea; dorsal root ganglion; and embryo. Orthologous to human EFHD1 (EF-hand domain family member D1).
PHENOTYPE: Mice homozygous for a null allele exhibit reduced axonal coverage and decreased number of branches with reduced ATP levels and shortened mitochondria in addition to increased neuron apoptosis. [provided by MGI curators]
  • synonyms:
  • EF hand domain containing 1,
  • expressed sequence AI452351,
  • AI452351,
  • 4931430I01Rik,
  • RIKEN cDNA 4931430I01 gene,
  • PP3051,
  • Efhd1,
  • MGI:2138258,
  • mitocalcin

Features --> Cross References

Genome

Sequence Feature Displayer

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0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

2 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

0 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