CNGB3

GENERAL INFORMATION

? »

Gene name

CNGB3

Gene description

Cyclic nucleotide gated channel beta 3

Protein class

Disease related genes
Potential drug targets
Predicted intracellular proteins
Predicted membrane proteins
Voltage-gated ion channels

Predicted localization

Intracellular,Membrane

Number of transcripts

2
SHOW MORE

HUMAN PROTEIN ATLAS INFORMATION

? »

RNA tissue category

HPA:Group enriched (fallopian tube, testis)
GTEx:Group enriched (fallopian tube, testis)

Protein evidence

Evidence at protein level

ANTIBODY RELIABILITY

? »

Data reliability

Pending normal tissue annotation.
SHOW MORE

RNA AND PROTEIN EXPRESSION SUMMARY

? »
RNA expression (FPKM) Protein expression (score)
Brain
N/A
Endocrine tissues
N/A
Bone marrow & immune system
N/A
Muscle tissues
N/A
Lung
N/A
Nasopharynx
N/A
N/A
Bronchus
N/A
N/A
Lung
N/A
Liver & gallbladder
N/A
Liver
N/A
Pancreas
N/A
Pancreas
N/A
Gastrointestinal tract
N/A
Kidney & urinary bladder
N/A
Male tissues
N/A
Testis
N/A
Epididymis
N/A
N/A
Prostate
N/A
Seminal vesicle
N/A
N/A
Female tissues
N/A
Breast
N/A
N/A
Vagina
N/A
N/A
Cervix, uterine
N/A
N/A
Ovary
N/A
Placenta
N/A
Adipose & soft tissue
N/A
Skin
N/A
Skin
N/A


PROTEIN EXPRESSION OVERVIEW

? »
Pending normal tissue annotation.


RNA EXPRESSION OVERVIEW

? »
HPA dataset
RNA tissue category:  Group enriched (fallopian tube, testis)

Organ

Expression

GTEx dataset
RNA tissue category:  Group enriched (fallopian tube, testis)

Organ

Expression



GENE INFORMATION

? »

Gene name

CNGB3 (HGNC Symbol)

Synonyms

ACHM1, ACHM3, RMCH

Description

Cyclic nucleotide gated channel beta 3 (HGNC Symbol)

Entrez gene summary

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]

Chromosome

8

Cytoband

q21.3

Chromosome location (bp)

86553977 - 86743675

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000170289 (version 78.38)

Entrez gene

54714

UniProt

Q9NQW8 (UniProt - Evidence at protein level)

neXtProt

NX_Q9NQW8

Antibodypedia

CNGB3 antibodies


PROTEIN BROWSER

? »
 
 
 
ENST00000320005
 
ENST00000517327
 
 
 
 


PROTEIN INFORMATION

? »

Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

CNGB3-001 ENSP00000316605
ENST00000320005
Q9NQW8
Show all »
Show » Show » 809 92.2 No 5
CNGB3-003 ENSP00000428329
ENST00000517327
H0YAZ4
Show all »
Show » 111 12.3 No 0