Clrn2 - clarin 2 Gene

Also Known as mpc169H; EG624224

Species: Mus musculus

Gene Type: protein coding
Gene ID: 624224

Summary

Acts upstream of or within inner ear auditory receptor cell differentiation; sensory perception of sound; and stereocilium maintenance. Located in stereocilium bundle. Human ortholog(s) of this gene implicated in autosomal recessive nonsyndromic deafness. Orthologous to human CLRN2 (clarin 2). [provided by Alliance of Genome Resources, Apr 2022]

Clrn2 Products (1)

mRNA Protein Name
NM_001163317.2 NP_001156789.1 clarin-2

Gene Ontology

  • Biological Process
  • Cellular Component
Biological Process GO Annotation Evidence References Source
involved in auditory receptor cell stereocilium organization IMP
IMP: Inferred from mutant phenotype
33496845 MGI
acts upstream of or within inner ear auditory receptor cell differentiation IMP
IMP: Inferred from mutant phenotype
31448880 MGI
acts upstream of or within sensory perception of sound IMP
IMP: Inferred from mutant phenotype
31448880 MGI
involved in sensory perception of sound IMP
IMP: Inferred from mutant phenotype
33496845 MGI
acts upstream of or within stereocilium maintenance IMP
IMP: Inferred from mutant phenotype
31448880 MGI
involved in stereocilium maintenance IMP
IMP: Inferred from mutant phenotype
33496845 MGI
Cellular Component GO Annotation Evidence References Source
located in stereocilium bundle IDA
IDA: Inferred from direct assay
31448880 MGI
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

clarin-2

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS02837 CLRN2 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens Clrn2 NCBI NCBI:645104