CNGA3 Products

Description

The CNGA3 gene encodes a member of the cyclic nucleotide-gated cation channel protein family which is required for normal vision and olfactory signal transduction. Mutations in this gene are associated with achromatopsia (rod monochromacy) and color blindness.

Bioinformatics

Entrez	1261 Human
Uniprot	NP_001289 Human NP_001073347 Human NP_001073347.1 Human
Product By Gene ID	1261
Alternate Names	CNG-3 cyclic nucleotide-gated cation channel alpha-3 CNCG3 cone photoreceptor cGMP-gated channel alpha subunit Cyclic nucleotide-gated channel alpha-3 Cone photoreceptor cGMP-gated channel subunit alpha CCNCa CCNCalpha CCNC1 CNG3ACHM2 CNG channel alpha-3 cyclic nucleotide gated channel alpha 3

Diseases related to CNGA3

Discover more about diseases related to CNGA3.

Achromatopsia
Color Vision Defect
Nystagmus
Photophobia
Retinal Diseases
Dystrophy
Blind Vision
Color Blindness
Retinal Degeneration
Pallor
Rod Monochromatism
Retinitis Pigmentosa
Retinal Dystrophies
Visual Impairment
Leber Congenital Amaurosis
Congenital Nystagmus
Amaurosis
Achromatopsia 2

Pathways for CNGA3

View related products by pathway and learn more about each of the pathways below.

Phototransduction
Localization
Cell Death
Transport
Reflex
Translation
Synaptic Transmission
Cellular Localization
Protein Folding
Protein Processing
Cell Adhesion
Cell Migration
Protein Maturation
Proteolysis
Hypersensitivity
Neurogenesis
Inflammatory Response
Sensitization
Reverse Transcription
Mating

PTMs for CNGA3

Learn more about PTMs related to CNGA3.

Phosphorylation
Cleavage

Bioinformatics Tool for CNGA3

Discover related pathways, diseases and genes to CNGA3. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.