GCK

GENERAL INFORMATION

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Gene name

GCK

Gene description

Glucokinase (hexokinase 4)

Protein class

Disease related genes
Enzymes
Potential drug targets
Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

6
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Mixed
GTEx:Tissue enhanced (liver)

Protein evidence

Evidence at protein level

Protein localization

Cytoplasmic expression in all tissues at variable levels. Highest levels in glandular epithelia of gastrointestinal tract.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 2 antibodies.
HPA007034 , HPA007093
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Pancreas

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Mixed

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (liver)

Organ

Expression



GENE INFORMATION

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Gene name

GCK (HGNC Symbol)

Synonyms

HK4, MODY2

Description

Glucokinase (hexokinase 4) (HGNC Symbol)

Entrez gene summary

Hexokinases phosphorylate glucose to produce glucose-6-phosphate, the first step in most glucose metabolism pathways. Alternative splicing of this gene results in three tissue-specific forms of glucokinase, one found in pancreatic islet beta cells and two found in liver. The protein localizes to the outer membrane of mitochondria. In contrast to other forms of hexokinase, this enzyme is not inhibited by its product glucose-6-phosphate but remains active while glucose is abundant. Mutations in this gene have been associated with non-insulin dependent diabetes mellitus (NIDDM), maturity onset diabetes of the young, type 2 (MODY2) and persistent hyperinsulinemic hypoglycemia of infancy (PHHI). [provided by RefSeq, Apr 2009]

Chromosome

7

Cytoband

p13

Chromosome location (bp)

44144271 - 44198170

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000106633 (version 78.38)

Entrez gene

2645

UniProt

P35557 (UniProt - Evidence at protein level)

neXtProt

NX_P35557

Antibodypedia

GCK antibodies


PROTEIN BROWSER

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ENST00000336642
 
ENST00000345378
 
ENST00000395796
 
ENST00000403799
 
ENST00000437084
 
ENST00000616242
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

GCK-001 ENSP00000384247
ENST00000403799
P35557
Show all »
Show » Show » 465 52.2 No 0
GCK-002 ENSP00000223366
ENST00000345378
P35557
Show all »
Show » Show » 466 52.1 No 0
GCK-003 ENSP00000379142
ENST00000395796
P35557
Show all »
Show » Show » 464 52 No 0
GCK-004 ENSP00000402840
ENST00000437084
C9JQD1
Show all »
Show » Show » 448 50.1 No 0
GCK-006 ENSP00000338009
ENST00000336642
H7BXV0
Show all »
Show » Show » 149 15.9 No 0
GCK-201 ENSP00000482149
ENST00000616242
P35557
Show all »
Show » Show » 464 52 No 0