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ENMouse
Clrn2 - clarin 2
Alias:
mpc169H
EG624224
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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]
Basic Information
NCBI
Transcripts
Exons
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Clrn2 Genetics information (+)
GRCm39
Sequence Homology
Transcripts & Proteins
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* This data comes from NCBI.
Gene Expression
Tissue-specific RNA expression
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Cell-specific RNA expression
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