hexokinase 1
| UniProt | Protein Name |
|---|---|
| A0A994J6R1 |
|
| A8K7J7 |
|
| A0A994J758 |
|
| P78542 |
|
| A0A994J4Q0 |
|
| B3KXY9 |
|
| A0A994J761 |
|
| P19367 |
|
| A0A994J753 |
|
| Q59FD4 |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| intracellular glucose homeostasis | ||
| positive regulation of cytokine production involved in immune response | ||
| fructose 6-phosphate metabolic process | ||
| glucose metabolic process | ||
| mannose metabolic process |
| GO Term | Evidence Code | PMID |
|---|---|---|
| mitochondrion | ||
| mitochondrion | ||
| mitochondrion | ||
| mitochondrion | ||
| mitochondrial outer membrane |
| GO Term | Evidence Code | PMID |
|---|---|---|
| glucokinase activity | ||
| glucokinase activity | ||
| glucokinase activity | ||
| hexokinase activity | ||
| protein binding |
| Gene Ontology |
|---|
| ATP binding |
| carbohydrate phosphorylation |
| fructokinase activity |
| glucokinase activity |
| glucose binding |
| glucose metabolic process |
| hexokinase activity |
| intracellular glucose homeostasis |
| kinase activity |
| mannokinase activity |
| InterPro |
|---|
| ATPase, nucleotide binding domain |
| Hexokinase, C-terminal |
| Hexokinase, N-terminal |
| Hexokinase, binding site |
| Hexokinase |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110196 | Charcot-Marie-Tooth disease type 4G | |
| DOID:10584 | retinitis pigmentosa | |
| DOID:2355 | anemia | |
| DOID:2861 | congenital nonspherocytic hemolytic anemia | |
| DOID:9538 | multiple myeloma | |
| DOID:9952 | acute lymphoblastic leukemia | |
| DOID:9970 | obesity |
| HPO ID | HPO Term |
|---|---|
| HP:0000006 | Autosomal dominant inheritance |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000219 | Thin upper lip vermilion |
| HP:0000286 | Epicanthus |
| HP:0000365 | Hearing impairment |
| HP:0000414 | Bulbous nose |
| HP:0000463 | Anteverted nares |
| HP:0000473 | Torticollis |
| HP:0000483 | Astigmatism |
| HP:0000486 | Strabismus |
| Disease ID | Disease Name |
|---|---|
| OMIM:618547 |
|
| OMIM:605285 |
|
| OMIM:617460 |
|
| ORPHA:99953 |
|
| OMIM:235700 |
|
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
This work is licensed under Creative Commons Attribution 4.0 International
GlyCosmos Portal v4.5.0
Last updated: April 6, 2026