1. Gene
  2. GNB2 - G protein subunit beta 2 Gene

GNB2 - G protein subunit beta 2 Gene

Homo sapiens

Also known as SSS4; HG2C1; SSS4; NEDHYDF

Gene ID: 2783 | Gene type: protein coding

About GNB2

Cytogenetic location: 7q22.1 Genomic coordinates (GRCh38): 7:100,673,740-100,679,169 (from NCBI)

This gene has 13 transcripts (splice variants), 194 orthologues, 4 paralogues and is associated with 3 phenotypes. Ubiquitous expression in esophagus (RPKM 67.4), prostate (RPKM 65.4) and 25 other tissues.

Summary

Heterotrimeric guanine nucleotide-binding proteins (G proteins), which integrate signals between receptors and effector proteins, are composed of an alpha, a beta, and a gamma subunit. These subunits are encoded by families of related genes. This gene encodes a beta subunit. Beta subunits are important regulators of alpha subunits, as well as of certain signal transduction receptors and effectors. This gene contains a trinucleotide (CCG) repeat length polymorphism in its 5' UTR. [provided by RefSeq, Jul 2008]

GNB2 Products(1)

mRNA Protein Name
NM_005273.4 NP_005264.2 guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-2

GNB2 Protein Structure

WD40

WD40: WD domain, G-beta repeat (49 - 83)

WD40

WD40: WD domain, G-beta repeat (96 - 125)

WD40

WD40: WD domain, G-beta repeat (137 - 170)

WD40

WD40: WD domain, G-beta repeat (178 - 212)

WD40

WD40: WD domain, G-beta repeat (218 - 254)

WD40

WD40: WD domain, G-beta repeat (272 - 298)

WD40

WD40: WD domain, G-beta repeat (306 - 340)

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  • 340 a.a.
Protein Preferred Names Protein Names

guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-2

G protein, beta-2 subunit

Related Diseases

Diseases Alias
Sick Sinus Syndrome 4

SSS4

Neurodevelopmental Disorder With Hypotonia And Dysmorphic Facies

NEDHYDF

Sturge-Weber Syndrome

SWS

Encephalotrigeminal Angiomatosis

Encephalofacial Angiomatosis

Sturge-Weber-Dimitri Syndrome

Sturge-Weber-Krabbe Syndrome

Fourth Phacomatosis

Leptomeningeal Angiomatosis

Meningeal Capillary Angiomatosis

Sturge-Weber-Krabbe Angiomatosis

Sturge-Weber Syndrome, Somatic, Mosaic

Sws Type I - Facial And Leptomeningeal Angiomas

Sws Type Ii - Facial Angioma Alone, No Cns Involvement

Sws Type Iii - Isolated Leptomeningeal Angiomas

Sturge Weber Syndrome

Angiomatosis Aculoorbital-Thalamic Syndrome

Encephalofacial Hemangiomatosis

Encephalofacial Hemangiomatosis Syndrome

Meningo-Oculo-Facial Angiomatosis

Meningofacial Angiomatosis-Cerebral Calcification Syndrome

Neuroretinoangiomatosis

Phakomatosis, Sturge-Weber

Weber-Sturge-Dimitri Syndrome

Sick Sinus Syndrome

Sinus Node Dysfunction

Sinus Node Disease

Sinus Node Infection

Snd

Sss

Snd - [Sinus Node Dysfunction]

Sinoatrial Node Dysfunction

Sss - [Sick Sinus Syndrome]

Sick Sinus

Sick Sinus Tachycardia

Night Blindness, Congenital Stationary, Type 1h

Congenital Stationary Night Blindness 1h

CSNB1H

Congenital Stationary Night Blindness Type 1h

Night Blindness, Congenital Stationary, 1h

Progressive Familial Heart Block, Type Ib

Progressive Familial Heart Block Type Ib

PFHB1B

Pfhbib

Progressive Familial Heart Block Type 1b

Heart Block Progressive Familial Type 1b

Progressive Familial Heart Block 1b

Cardiac Conduction Block

Right-Bundle Branch Block

Heart Block, Familial, Progressive, Type 1b

Heart Block

Right Bundle Branch Block

Weber Syndrome

Midbrain Stroke Syndromes

Night Blindness, Congenital Stationary, Autosomal Dominant 2

Congenital Stationary Night Blindness Autosomal Dominant 2

CSNBAD2

Hemeralopia

Night Blindness, Congenital Stationary, Rambusch Type

Rambusch Type Congenital Stationary Night Blindness

Congenital Stationary Night Blindness Rambusch Type

Hemeralopia Congenital Essential

Blindness, Night, Stationary, Congenital, Autosomal Dominant, Type 2

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus GNB2 RGD RGD:69319
Mus musculus GNB2 MGD MGI:95784
Canis familiaris GNB2 VGNC VGNC:41313
Macaca mulatta GNB2 VGNC VGNC:81318
Felis catus GNB2 VGNC VGNC:62621
Bos taurus GNB2 VGNC VGNC:29459
Others GNB2 NCBI