HK1
Strwythurau PDB Human UniProt search:PDBeRCSB Rhestr o ddynodwyr PDB 1CZA,1DGK,1HKB,1HKC,1QHA,4F9O,4FOE,4FOI,4FPA,4FPB
Dynodwyr
Cyfenwau	HK1, HK1-ta, HK1-tb, HK1-tc, HKD, HKI, HMSNR, HXK1, hexokinase 1, HK, hexokinase, RP79, NEDVIBA
Dynodwyr allanol	OMIM:142600HomoloGene:100530GeneCards:HK1
PatrwmRNA pattern Rhagor o gyfeiriadau
Ontoleg y genyn Gweithrediad moleciwlaidd •transferase activity •nucleotide binding •mannokinase activity •phosphotransferase activity, alcohol group as acceptor •kinase activity •glucose binding •catalytic activity •GO:0001948, GO:0016582 protein binding •fructokinase activity •ATP binding •glucokinase activity •hexokinase activity •peptidoglycan binding •identical protein binding Cydrannau o'r gell •cytosol •bilen •cilium •mitochondrial outer membrane •sperm principal piece •mitocondria •membrane raft Prosesau biolegol •glycolytic process •phosphorylation •canonical glycolysis •cellular glucose homeostasis •maintenance of protein location in mitochondrion •establishment of protein localization to mitochondrion •hexose metabolic process •metabolaeth •glucose 6-phosphate metabolic process •carbohydrate metabolic process •carbohydrate phosphorylation Sources:Amigo /QuickGO
Orthologau
Species	Bod dynol	Llygoden
Entrez	3098	n/a
Ensembl	ENSG00000156515	n/a
UniProt	P19367	n/a
RefSeq (mRNA)	NM_000188 NM_033496 NM_033497 NM_033498 NM_033500 NM_001322364 NM_001322365 NM_001322366 NM_001322367 NM_001358263	n/a
RefSeq (protein)	NP_000179 NP_001309293 NP_001309294 NP_001309295 NP_001309296 NP_277031 NP_277032 NP_277033 NP_277035 NP_001345192	n/a
Lleoliad (UCSC)	n/a	n/a
PubMed search	[1]	n/a
Wicidata
Gweld/Golygu Bod dynol

Protein sy'n cael ei godio yn ycorff dynol gan y genynHK1 ywHK1 a elwir hefyd ynPhosphotransferase a Hexokinase 1 (Saesneg). Segment oDNA yw'rgenyn, sy'n amgodio ffwythiant arbennig. Mae'r genyn yma wedi ei leoli ar yr edefyn blaen o gromosom dynol 10, band 10q22.1.^[2]

Yn aml mae gan enynnau lawer o gyfystyron. Mae hyn oherwydd eu bod yn aml yn cael eu darganfod gan nifer o bobl mewn cyd-destunau gwahanol heb wybod mai'r un genynnau oeddyn nhw. Hefyd mae gan wahanol gymunedau gwyddonol safonau gwahanol ar gyfer enwi genynnau. Dyma restr o gyfystyron ar gyfer y genyn HK1.

• "HSMNR belongs to the most frequent types of hereditary neuropathy in the Czech Republic and is twice more frequent than HMSNL.". Clin Genet. 2016. PMID 26822750.
• "Overexpression of Hexokinase 1 as a poor prognosticator in human colorectal cancer.". Tumour Biol. 2016. PMID 26476538.
• "Identification of a Novel Gene on 10q22.1 Causing Autosomal Dominant Retinitis Pigmentosa (adRP).". Adv Exp Med Biol. 2016. PMID 26427411.
• "A missense mutation in HK1 leads to autosomal dominant retinitis pigmentosa.". Invest Ophthalmol Vis Sci. 2014. PMID 25316723.
• "A dominant mutation in hexokinase 1 (HK1) causes retinitis pigmentosa.". Invest Ophthalmol Vis Sci. 2014. PMID 25190649.

• Genes on human chromosome
• Genynnau

• Erthyglau Bot Wici-Iechyd