GNB3
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 12[13]
- Cytogenetic location
- 12p13.31[16]
- Encodes
- G protein subunit beta 3, Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-3[10][11]
- Expressed in
- anterior pituitary, right hemisphere of cerebellum, apex of heart, right frontal lobe, right ovary, retinal pigment epithelium, right coronary artery, body of uterus, left ovary, Descending thoracic aorta[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- congenital stationary night blindness 1H[14]
- HomoloGene ID
- 55628[3]
- Strand orientation
- forward strand[15]
🏷️ Also known as
en CSNB1H
en GNB3
en G protein subunit beta 3
en HG2D
ar GNB٣
🔖 Identifiers · 11
- Ensembl gene ID
- ENSG00000111664
- Ensembl transcript ID
- ENST00000542868, ENST00000229264, ENST00000435982, ENST00000537035, ENST00000539127, ENST00000540458, ENST00000541257, ENST00000541978, ENST00000542751, ENST00000675241
- Entrez Gene ID
- 2784
- Exact match
- identifiers.org
- Freebase ID
- /m/03c_z3y
- HGNC ID
- 4400
- HGNC gene symbol
- GNB3
- Microsoft Academic ID (discontinued)
- 2779182101
- OMIM ID
- 139130
- RefSeq RNA ID
- NM_001297571, NM_002075, XM_011520953, XM_047428702, XM_047428703
- UMLS CUI
- C1333689
🔗 Connections
Expressed in 3
Chromosome 1
Found in taxon 1
Instance of 1
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