Efhc1 Gene Summary [Mouse]

Predicted to enable alpha-tubulin binding activity. Involved in flagellated sperm motility. Located in axoneme and neuronal cell body. Is active in axonemal A tubule inner sheath and sperm flagellum. Is expressed in several structures, including brain; epithelium; future hindbrain roof plate; spinal cord ventricular layer; and spleen. Used to study juvenile myoclonic epilepsy. Human ortholog(s) of this gene implicated in juvenile absence epilepsy 1 and juvenile myoclonic epilepsy. Orthologous to human EFHC1 (EF-hand domain containing 1). [provided by Alliance of Genome Resources, Jul 2025]

Details

Type
Processed Transcript
Official Symbol
Efhc1
Official Name
EF-hand domain (C-terminal) containing 1 [Source:MGI Symbol;Acc:MGI:1919127]
Ensembl ID
ENSMUSG00000041809
Bio databases IDs NCBI: 71877 Ensembl: ENSMUSG00000041809
Aliases EF-hand domain (C-terminal) containing 1
Synonyms 1700029F22RIK, dJ304B14.2, EF-hand domain containing 1, EF-hand domain (C-terminal) containing 1, EJM1, LOC684521, mRib72-1, myoclonin1, POC9, RIB72
Species
Mouse, Mus musculus
OrthologiesHumanRat

Protein Domains

A protein domain is a distinct structural or functional region within a protein that can evolve, function, and exist independently of the rest of the protein chain. These domains in mouse Efhc1 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • EF-hand, calcium binding motif
  • EF-hand domain
  • DM10 domain
  • EF-hand domain pair
  • alpha-tubulin binding
  • EFh
  • protein binding
  • Domains in hypothetical proteins in Drosophila, C

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • seizures
  • myocarditis
  • susceptibility to juvenile myoclonic epilepsy type 1
  • peripheral arterial disease
  • susceptibility to juvenile absence epilepsy type 1
  • juvenile myoclonic epilepsy
  • myoclonus
  • epilepsy
  • absence seizure
  • atopic dermatitis
regulated by
regulates
  • voltage-gated calcium channel
role in cell
  • migration
  • apoptosis
  • motility
  • organization
  • cell division

Subcellular Expression

Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
  • Cytoplasm
  • cilia
  • centrosome
  • axonemes
  • spindle pole
  • sperm tail
  • mitotic spindle
  • perikaryon

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the mouse Efhc1 gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • regulation of cell division
  • mitotic spindle organization
  • cytokinesis after mitosis
  • ciliary cell motility
  • cerebral cortex cell migration

Cellular Component

Where in the cell the gene product is active
  • centrosome
  • axonemal microtubule
  • mitotic spindle
  • spindle pole
  • neuronal cell body
  • axoneme

Molecular Function

What the gene product does at the molecular level
  • protein binding
  • calcium ion binding
  • alpha-tubulin binding

Gene-Specific Assays for Results You Can Trust

Streamline your workflow with assays designed for this gene. Our targeted dPCR and qPCR assays help you generate meaningful data – efficiently and accurately.