CHRND

GENERAL INFORMATION

? »

Gene name

CHRND

Gene description

Cholinergic receptor, nicotinic, delta (muscle)

Protein class

Disease related genes
Potential drug targets
Predicted membrane proteins
Predicted secreted proteins
Transporters

Predicted localization

Membrane,Secreted

Number of transcripts

3
SHOW MORE

HUMAN PROTEIN ATLAS INFORMATION

? »

RNA tissue category

HPA:Tissue enriched (skeletal muscle)
GTEx:Tissue enriched (skeletal muscle)

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:  Tissue enriched (skeletal muscle)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enriched (skeletal muscle)

Organ

Expression



GENE INFORMATION

? »

Gene name

CHRND (HGNC Symbol)

Synonyms

ACHRD

Description

Cholinergic receptor, nicotinic, delta (muscle) (HGNC Symbol)

Entrez gene summary

The acetylcholine receptor of muscle has 5 subunits of 4 different types: 2 alpha and 1 each of beta, gamma and delta subunits. After acetylcholine binding, the receptor undergoes an extensive conformation change that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane. Defects in this gene are a cause of multiple pterygium syndrome lethal type (MUPSL), congenital myasthenic syndrome slow-channel type (SCCMS), and congenital myasthenic syndrome fast-channel type (FCCMS). Several transcript variants, some protein-coding and some not, have been found for this gene. [provided by RefSeq, Feb 2012]

Chromosome

2

Cytoband

q37.1

Chromosome location (bp)

232525993 - 232536667

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000135902 (version 78.38)

Entrez gene

1144

UniProt

Q07001 (UniProt - Evidence at protein level)

neXtProt

NX_Q07001

Antibodypedia

CHRND antibodies


PROTEIN BROWSER

? »
 
 
 
ENST00000258385
 
ENST00000449596
 
ENST00000543200
 
 
 
 


PROTEIN INFORMATION

? »

Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

CHRND-001 ENSP00000258385
ENST00000258385
Q07001
Show all »
Show » Show » 517 58.9 Yes 4
CHRND-003 ENSP00000404950
ENST00000449596
C9JJV8
Show all »
Show » Show » 172 19.6 Yes 0
CHRND-201 ENSP00000438380
ENST00000543200
Q07001
Show all »
Show » Show » 502 57.1 Yes 4