1. Gene
  2. GK2 - glycerol kinase 2 Gene

GK2 - glycerol kinase 2 Gene

Homo sapiens

Also known as GKP2; GKTA

Gene ID: 2712 | Gene type: protein coding

About GK2

Cytogenetic location: 4q21.21 Genomic coordinates (GRCh38): 4:79,406,361-79,408,228 (from NCBI)

This gene has 1 transcript (splice variant), 246 orthologues and 6 paralogues.

Summary

Predicted to enable glycerol kinase activity. Predicted to be involved in several processes, including glycerol metabolic process; glycerol-3-phosphate biosynthetic process; and triglyceride metabolic process. Located in extracellular exosome. [provided by Alliance of Genome Resources, Apr 2022]

GK2 Products(1)

mRNA Protein Name
NM_033214.3 NP_149991.2 glycerol kinase 2

GK2 Protein Structure

FGGY_N

FGGY_N: FGGY family of carbohydrate kinases, N-terminal domain (14 - 266)

FGGY_C

FGGY_C: FGGY family of carbohydrate kinases, C-terminal domain (275 - 466)

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  • 553 a.a.
Protein Preferred Names Protein Names

glycerol kinase 2

ATP:glycerol 3-phosphotransferase 2

Related Diseases

Diseases Alias
Glycerol Kinase Deficiency

Hyperglycerolemia

GKD

Gk Deficiency

Gk1 Deficiency

Deficiency Of Glycerol Kinase

Isolated Glycerol Kinase Deficiency

Glycerol Kinase Deficiency, Adult Form

Glycerol Kinase Deficiency, Juvenile Form

Deficiency, Glycerol Kinase

Hypoadrenocorticism, Familial

Addison Disease

Primary Adrenocortical Insufficiency

Addison'S Disease

Adrenal Gland Hypofunction

Adrenal Hypoplasia

Adrenal Aplasia

Addison Disease, Chronic Adrenal Insufficiency

Primary Hypoadrenalism

Hypoadrenocorticism Familial

Autoimmune Addison Disease

Autoimmune Adrenalitis

Classic Addison Disease

Primary Addison Disease

Addisons Disease

Addison Disease, Susceptibility To

Autoimmune Primary Adrenal Insufficiency

Addison'S Disease Due To Autoimmunity

Muscular Dystrophy, Duchenne Type

Duchenne Muscular Dystrophy

DMD

Muscular Dystrophy, Duchenne

Muscular Dystrophy, Pseudohypertrophic Progressive, Duchenne Type

Severe Dystrophinopathy, Duchenne Type

Muscular Dystrophy Duchenne

Dystrophy, Muscular, Duchenne Type

Benign Duchenne Muscular Dystrophy

Duchenne Motor Neuron Disease

Duchenne Type Dystrophy

Duchenne-Griesinger Disease

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
Canis familiaris GK2 VGNC VGNC:57407
Rattus norvegicus GK2 RGD RGD:1303263
Mus musculus GK2 MGD MGI:1329027
Macaca mulatta GK2 VGNC VGNC:106585
Others GK2 NCBI