CHGB (chromogranin B)

2011-04-01  

Identity

HGNC
LOCATION
20p12.3
LOCUSID
ALIAS
SCG1
FUSION GENES

Other Information

Locus ID:

NCBI: 1114
MIM: 118920
HGNC: 1930
Ensembl: ENSG00000089199

Variants:

dbSNP: 1114
ClinVar: 1114
TCGA: ENSG00000089199
COSMIC: CHGB

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000089199ENST00000378961P05060
ENSG00000089199ENST00000455042A0A0A0MT66

Expression (GTEx)

0
500
1000
1500
2000

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
199131212009Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.85
200073712009Chromogranin B P413L variant as risk factor and modifier of disease onset for amyotrophic lateral sclerosis.20
200073712009Chromogranin B P413L variant as risk factor and modifier of disease onset for amyotrophic lateral sclerosis.20
152194672004Association between chromogranin b gene polymorphisms and schizophrenia in the Japanese population.11
152194672004Association between chromogranin b gene polymorphisms and schizophrenia in the Japanese population.11
206280862010Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.11
119594262002Polymorphisms of chromogranin B gene associated with schizophrenia in Chinese Han population.10
119594262002Polymorphisms of chromogranin B gene associated with schizophrenia in Chinese Han population.10
126924772003Different chromogranin immunoreactivity between prion and a-beta amyloid plaque.10
187218312009Chromogranin peptides in amyotrophic lateral sclerosis.10

Citation

Dessen P

CHGB (chromogranin B)

Atlas Genet Cytogenet Oncol Haematol. 2011-04-01

Online version: http://atlasgeneticsoncology.org/gene/52182/chgb