Homo Sapiens
CNGB3 - Cyclic Nucleotide Gated Channel Subunit Beta 3
Alias:
ACHM1
This gene encodes the beta subunit of a cyclic nucleotide-gated ion channel. The encoded beta subunit appears to play a role in modulation of channel function in cone photoreceptors. This heterotetrameric channel is necessary for sensory transduction, and mutations in this gene have been associated with achromatopsia 3, progressive cone dystrophy, and juvenile macular degeneration, also known as Stargardt Disease. [provided by RefSeq, Feb 2010]
Basic Information
NCBI
Transcripts
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MW (kDa)
Mutations
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Reference
CNGB3 Genetics information (-)
GRCh38
Chr : -
Sequence Homology
Selected Gene:
Human：CNGB3
Disease & Mutation
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* This data comes from NCBI.
Gene Expression
Tissue-specific RNA expression
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