1. Gene
  2. FBP2 - fructose-bisphosphatase 2 Gene

FBP2 - fructose-bisphosphatase 2 Gene

Homo sapiens

Also known as CORLK

Gene ID: 8789 | Gene type: protein coding

About FBP2

Cytogenetic location: 9q22.32 Genomic coordinates (GRCh38): 9:94,558,720-94,593,824 (from NCBI)

This gene has 1 transcript (splice variant), 198 orthologues, 1 paralogue and is associated with 1 phenotype. Biased expression in stomach (RPKM 15.5), esophagus (RPKM 4.0) and 3 other tissues.

Summary

This gene encodes a gluconeogenesis regulatory Enzyme which catalyzes the hydrolysis of fructose 1,6-bisphosphate to fructose 6-phosphate and inorganic phosphate. [provided by RefSeq, Jul 2008]

FBP2 Products(1)

mRNA Protein Name
NM_003837.4 NP_003828.2 fructose-1,6-bisphosphatase isozyme 2
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference Source
enables identical protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

FBP2 Protein Structure

FBPase

FBPase: Fructose-1-6-bisphosphatase, N-terminal domain (13 - 333)

  • 0
  • 100
  • 200
  • 300
  • 339 a.a.
Protein Preferred Names Protein Names

fructose-1,6-bisphosphatase isozyme 2

D-fructose-1,6-bisphosphate 1-phosphohydrolase 2

Related Diseases

Diseases Alias
Leukodystrophy, Childhood-Onset, Remitting

CORLK

Fructose-1,6-Bisphosphatase Deficiency

Fructose-1,6-Diphosphatase Deficiency

Baker-Winegrad Disease

FBP1D

Fbpase Deficiency

Fructose 1,6 Diphosphatase Deficiency

Fructose 1 Phosphate Aldolase Deficiency

Fbp1 Deficiency

Hereditary Fructose Intolerance Syndrome

Glycogen Storage Disease

Glycogenosis

Glycogenoses

Gsd

Storage Disease, Glycogen

Gsd - [Glycogen Storage Disease]

Glycogen Thesaurismosis

Diffuse Glycogenosis

Generalised Glycogen Storage Disease

Generalised Glycogenosis

Generalised Glycogen Storage Disease Of Infants

Glycogen Synthase Deficiency

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
Felis catus FBP2 VGNC VGNC:62173
Rattus norvegicus FBP2 RGD RGD:620930
Macaca mulatta FBP2 VGNC VGNC:72626
Bos taurus FBP2 VGNC VGNC:28888
Canis familiaris FBP2 VGNC VGNC:49894
Mus musculus FBP2 MGD MGI:95491
Macaca fascicularis FBP2 NCBI NCBI:102142152
Others FBP2 NCBI