Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
3795
Gene name Gene Name - the full gene name approved by the HGNC.
Ketohexokinase
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
KHK
Synonyms (NCBI Gene) Gene synonyms aliases
FRUCTU
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2p23.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes ketohexokinase that catalyzes conversion of fructose to fructose-1-phosphate. The product of this gene is the first enzyme with a specialized pathway that catabolizes dietary fructose. Alternatively spliced transcript variants encoding d
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs104893643 G>A,C Affects Coding sequence variant, intron variant, missense variant
rs104893644 G>A Affects Coding sequence variant, intron variant, missense variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT019807 hsa-miR-375 Microarray 20215506
MIRT029406 hsa-miR-26b-5p Microarray 19088304
MIRT1085251 hsa-miR-3667-5p CLIP-seq
MIRT1085252 hsa-miR-4762-5p CLIP-seq
MIRT1085253 hsa-miR-1207-5p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0004454 Function Ketohexokinase activity IBA
GO:0004454 Function Ketohexokinase activity IDA 12941785, 22371574
GO:0004454 Function Ketohexokinase activity IEA
GO:0004454 Function Ketohexokinase activity TAS 7833921
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
614058 6315 ENSG00000138030
Protein
UniProt ID P50053
Protein name Ketohexokinase (EC 2.7.1.3) (Hepatic fructokinase)
Protein function Catalyzes the phosphorylation of the ketose sugar fructose to fructose-1-phosphate.
PDB 2HLZ , 2HQQ , 2HW1 , 3B3L , 3NBV , 3NBW , 3NC2 , 3NC9 , 3NCA , 3Q92 , 3QA2 , 3QAI , 3RO4 , 5WBM , 5WBO , 5WBP , 5WBQ , 5WBR , 5WBZ , 6UL7 , 6W0N , 6W0W , 6W0X , 6W0Y , 6W0Z , 8OME , 8OMF , 8OMJ , 8OMK , 8UG1 , 8UG3 , 9FHD , 9FHE
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00294 PfkB 3 294 pfkB family carbohydrate kinase Family
Tissue specificity TISSUE SPECIFICITY: Most abundant in liver, kidney, gut, spleen and pancreas. Low levels also found in adrenal, muscle, brain and eye. {ECO:0000269|PubMed:9799106}.
Sequence
Sequence length 298
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Fructose and mannose metabolism
Metabolic pathways
  Essential fructosuria
Fructose catabolism
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Disease merge term Disease name dbSNP ID References
Fructosuria essential fructosuria rs104893644 N/A
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Adenoma Associate 24567419
Carcinoma Hepatocellular Associate 29449409
Carcinoma Renal Cell Associate 15953868
Endometrial Neoplasms Associate 39465767
Fructosuria Associate 19237742, 33621267
Inflammation Associate 36194576
Neoplasms Associate 24567419
Pulmonary Disease Chronic Obstructive Associate 36194576