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GLYCOLYSIS PATHWAY (PW:0000640)

View Ontology Report

Description

Glucose is a major source of energy in the cell. In the first round of breakdown - a pathway known as glycolysis, one of the best characterized biochemical pathways - one molecule of glucose is converted to two molecules of pyruvate with a net yield of 2 ATP and the reduction of 2 NAD+ to 2 NADH. The 10 enzymatic reactions of glycolysis can be divided into two stages: an energy consumption stage I (reactions 1 to 5) and an energy recovery/generation stage II (reactions 6 to 10)

Pathway Diagram:

Ariadne Genomics Inc. phosphoenolpyruvate gluconeogenesis pathway pyruvate metabolic pathway aldolases Pfkfb members (kinase) Pfkfb members (phosphatase) phosphofructokinases enolases hexokinases ATP ---| phosphofructokinases F2,6P --+> phosphofructokinases AMP --+> phosphofructokinases Tpi1 glyceraldehyde-3-phosphate <--> dihydroxyacetone-phosphate Gapdh Pgk1 Pgam2 Pkm2 Gpi glucose Pfkfb members (phosphatase) ---| F2,6P phosphoenolpyruvate ---> pyruvate glyceraldehyde-3-phosphate <--> 1,3-biphosphoglycerate fructose-1,6-diphosphate <--> glyceraldehyde-3-phosphate 3-phosphoglycerate <--> 2-phosphoglycerate pyruvate ---> pyruvate metabolic pathway pyruvate fructose-6-phosphate ---> fructose-1,6-diphosphate Pfkfb members (kinase) --+> F2,6P ATP ---- phosphofructokinases pyruvate ---> gluconeogenesis pathway glucose-6-phosphate <--> fructose-6-phosphate fructose-1,6-diphosphate <--> dihydroxyacetone-phosphate AMP F2,6P 3-phosphoglycerate <--> 1,3-biphosphoglycerate 1,3-biphosphoglycerate 3-phosphoglycerate 2-phosphoglycerate glucose-6-phosphate fructose-6-phosphate ATP fructose-1,6-diphosphate dihydroxyacetone-phosphate glyceraldehyde-3-phosphate Pklr 2-phosphoglycerate <--> phosphoenolpyruvate glucose ---> glucose-6-phosphate
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Genes in Pathway:


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glycolysis pathway term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Acss1 acyl-CoA synthetase short-chain family member 1 IEA KEGG rno:00010 NCBI chr 3:139,450,383...139,500,325
Ensembl chr 3:139,450,383...139,500,325
JBrowse link
G Acss2 acyl-CoA synthetase short-chain family member 2 IEA KEGG rno:00010 NCBI chr 3:144,003,808...144,047,452
Ensembl chr 3:144,004,336...144,059,675
JBrowse link
G Adh4 alcohol dehydrogenase 4 (class II), pi polypeptide IEA KEGG rno:00010 NCBI chr 2:226,948,717...226,966,747
Ensembl chr 2:226,947,466...226,987,591
JBrowse link
G Adh5 alcohol dehydrogenase 5 (class III), chi polypeptide IEA KEGG rno:00010 NCBI chr 2:226,975,184...226,987,591
Ensembl chr 2:226,947,466...226,987,591
JBrowse link
G Adh6 alcohol dehydrogenase 6 (class V) IEA KEGG rno:00010 NCBI chr 2:226,903,208...226,934,564
Ensembl chr 2:226,903,250...226,934,534
JBrowse link
G Adh7 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide IEA KEGG rno:00010 NCBI chr 2:226,748,724...226,763,183
Ensembl chr 2:226,741,788...226,763,182
JBrowse link
G Adpgk ADP-dependent glucokinase IEA KEGG rno:00010 NCBI chr 8:59,699,400...59,727,352
Ensembl chr 8:59,699,388...59,727,351
JBrowse link
G Akr1a1 aldo-keto reductase family 1 member A1 IEA KEGG rno:00010 NCBI chr 5:130,092,945...130,130,277
Ensembl chr 5:130,092,732...130,113,674
JBrowse link
G Aldh1a1 aldehyde dehydrogenase 1 family, member A1 IEA KEGG rno:00010 NCBI chr 1:218,000,470...218,152,962
Ensembl chr 1:218,042,127...218,152,961
JBrowse link
G Aldh1a3 aldehyde dehydrogenase 1 family, member A3 IEA KEGG rno:00010 NCBI chr 1:119,982,272...120,017,416
Ensembl chr 1:119,982,277...120,017,436
JBrowse link
G Aldh1a7 aldehyde dehydrogenase family 1, subfamily A7 IEA KEGG rno:00010 NCBI chr 1:218,201,443...218,241,410 JBrowse link
G Aldh1b1 aldehyde dehydrogenase 1 family, member B1 IEA KEGG rno:00010 NCBI chr 5:60,063,370...60,068,378
Ensembl chr 5:60,063,225...60,068,378
JBrowse link
G Aldh2 aldehyde dehydrogenase 2 family member IEA KEGG rno:00010 NCBI chr12:34,949,549...34,982,527
Ensembl chr12:34,901,219...34,982,521
JBrowse link
G Aldh3a1 aldehyde dehydrogenase 3 family, member A1 IEA KEGG rno:00010 NCBI chr10:45,892,993...45,902,680
Ensembl chr10:45,892,924...45,902,681
JBrowse link
G Aldh3a2 aldehyde dehydrogenase 3 family, member A2 IEA KEGG rno:00010 NCBI chr10:45,928,313...45,949,366
Ensembl chr10:45,908,524...45,949,281
JBrowse link
G Aldh3b1 aldehyde dehydrogenase 3 family, member B1 IEA KEGG rno:00010 NCBI chr 1:201,145,309...201,162,675
Ensembl chr 1:201,145,309...201,163,921
JBrowse link
G Aldh7a1 aldehyde dehydrogenase 7 family, member A1 IEA KEGG rno:00010 NCBI chr18:50,003,242...50,042,193
Ensembl chr18:50,009,934...50,042,193
JBrowse link
G Aldh9a1 aldehyde dehydrogenase 9 family, member A1 IEA KEGG rno:00010 NCBI chr13:79,505,738...79,522,539
Ensembl chr13:79,505,695...79,540,568
JBrowse link
G Aldoa aldolase, fructose-bisphosphate A ISO
IEA
KEGG
SMPDB
RGD
PMID:5251864 SMP:00040 rno:00010, RGD:2302796 NCBI chr 1:181,402,275...181,407,476
Ensembl chr 1:181,402,275...181,406,182
JBrowse link
G Aldoart2 aldolase 1 A retrogene 2 ISO SMPDB
RGD
PMID:5251864 RGD:2302796 SMP:00040 NCBI chr 6:72,939,821...72,941,511
Ensembl chr 6:72,939,788...72,941,709
JBrowse link
G Aldob aldolase, fructose-bisphosphate B ISO
IEA
KEGG
RGD
PMID:5251864 rno:00010, RGD:2302796 NCBI chr 5:63,889,045...63,902,086
Ensembl chr 5:63,889,046...63,902,116
JBrowse link
G Aldoc aldolase, fructose-bisphosphate C IEA KEGG rno:00010 NCBI chr10:63,217,477...63,221,066
Ensembl chr10:63,217,451...63,221,066
JBrowse link
G Bpgm bisphosphoglycerate mutase IEA
ISO
KEGG
SMPDB
SMP:00040 rno:00010 NCBI chr 4:63,139,730...63,168,581
Ensembl chr 4:63,140,018...63,168,581
JBrowse link
G Dlat dihydrolipoamide S-acetyltransferase IEA KEGG rno:00010 NCBI chr 8:50,979,151...51,004,435
Ensembl chr 8:50,978,051...51,004,479
JBrowse link
G Dld dihydrolipoamide dehydrogenase IEA KEGG rno:00010 NCBI chr 6:47,904,153...47,924,814
Ensembl chr 6:47,903,914...47,924,795
JBrowse link
G Eno1 enolase 1 ISO
IEA
KEGG
SMPDB
RGD
PMID:18560153 SMP:00040 rno:00010, RGD:2302799 NCBI chr 5:160,719,951...160,731,337
Ensembl chr 5:160,719,951...160,731,336
JBrowse link
G Eno2 enolase 2 IEA KEGG rno:00010 NCBI chr 4:157,572,085...157,580,971
Ensembl chr 4:157,572,088...157,580,980
JBrowse link
G Eno3 enolase 3 IEA KEGG rno:00010 NCBI chr10:55,370,531...55,375,921
Ensembl chr10:55,366,975...55,375,921
JBrowse link
G Fbp1 fructose-bisphosphatase 1 IEA KEGG rno:00010 NCBI chr17:2,207,271...2,230,076
Ensembl chr17:2,208,031...2,230,071
JBrowse link
G Fbp2 fructose-bisphosphatase 2 IEA KEGG rno:00010 NCBI chr17:2,236,088...2,253,702
Ensembl chr17:2,236,336...2,253,698
JBrowse link
G G6pc1 glucose-6-phosphatase catalytic subunit 1 IEA
ISO
KEGG
SMPDB
SMP:00040 rno:00010 NCBI chr10:86,307,400...86,318,766
Ensembl chr10:86,257,668...86,333,804
JBrowse link
G Galm galactose mutarotase IEA
ISO
KEGG
SMPDB
SMP:00040 rno:00010 NCBI chr 6:14,837,540...14,889,484
Ensembl chr 6:14,837,548...14,889,310
JBrowse link
G Gapdh glyceraldehyde-3-phosphate dehydrogenase IEA
ISO
KEGG
SMPDB
SMP:00040 rno:00010 NCBI chr 4:157,962,312...157,967,158
Ensembl chr 4:157,962,343...157,966,235
JBrowse link
G Gapdh-ps118 Glyceraldehyde-3-phosphate dehydrogenase, pseudogene 118 IEA KEGG rno:00010 NCBI chr18:61,626,988...61,628,224
Ensembl chr 4:157,962,343...157,966,235
JBrowse link
G Gapdhl10 glyceraldehyde-3-phosphate dehydrogenase like 10 IEA KEGG rno:00010 NCBI chr16:15,370,290...15,371,300
Ensembl chr16:15,370,293...15,371,300
JBrowse link
G Gapdhl3 glyceraldehyde-3-phosphate dehydrogenase like 3 IEA KEGG rno:00010 NCBI chr15:77,324,675...77,471,131 JBrowse link
G Gapdhl9 glyceraldehyde-3-phosphate dehydrogenase like 9 IEA KEGG rno:00010 NCBI chr 2:210,784,633...210,785,652 JBrowse link
G Gapdhs glyceraldehyde-3-phosphate dehydrogenase, spermatogenic IEA KEGG rno:00010 NCBI chr 1:85,979,096...85,994,153
Ensembl chr 1:85,979,098...85,993,640
JBrowse link
G Gck glucokinase TAS
IDA
IEA
KEGG
RGD
PMID:9540816 PMID:4273555 PMID:4353083 rno:00010, RGD:2302784, RGD:2302790, RGD:2302851 NCBI chr14:80,785,060...80,829,842
Ensembl chr14:80,785,060...80,826,995
JBrowse link
G Gpi glucose-6-phosphate isomerase IEA
ISO
KEGG
SMPDB
SMP:00040 rno:00010 NCBI chr 1:86,828,211...86,856,077
Ensembl chr 1:86,828,216...86,856,086
JBrowse link
G Hk1 hexokinase 1 TAS
IDA
IEA
KEGG
RGD
PMID:9540816 PMID:4353083 rno:00010, RGD:2302784, RGD:2302851 NCBI chr20:30,230,488...30,332,099
Ensembl chr20:30,230,486...30,332,131
JBrowse link
G Hk2 hexokinase 2 TAS
IEA
ISO
KEGG
SMPDB
RGD
PMID:9540816 SMP:00040 rno:00010, RGD:2302784 NCBI chr 4:115,234,509...115,283,530
Ensembl chr 4:115,234,509...115,283,530
JBrowse link
G Hk3 hexokinase 3 TAS
IEA
KEGG
RGD
PMID:9540816 rno:00010, RGD:2302784 NCBI chr17:9,596,950...9,614,847
Ensembl chr17:9,599,865...9,614,863
JBrowse link
G Ldha lactate dehydrogenase A IEA KEGG rno:00010 NCBI chr 1:97,371,823...97,381,247
Ensembl chr 1:97,366,021...97,433,472
JBrowse link
G Ldhal1 lactate dehydrogenase A like 1 IEA KEGG rno:00010 NCBI chr 8:30,363,220...30,364,836 JBrowse link
G Ldhal6b lactate dehydrogenase A-like 6B IEA KEGG rno:00010 NCBI chr 1:45,997,845...45,999,268
Ensembl chr 1:45,991,991...45,999,272
JBrowse link
G Ldhb lactate dehydrogenase B IEA KEGG rno:00010 NCBI chr 4:175,428,382...175,446,403
Ensembl chr 4:175,428,385...175,446,403
JBrowse link
G Ldhc lactate dehydrogenase C IEA KEGG rno:00010 NCBI chr 1:97,385,984...97,403,382
Ensembl chr 1:97,382,379...97,403,378
JBrowse link
G Pank1 pantothenate kinase 1 ISO SMPDB SMP:00040 NCBI chr 1:232,324,718...232,395,445
Ensembl chr 1:232,328,430...232,396,829
JBrowse link
G Pck1 phosphoenolpyruvate carboxykinase 1 IEA KEGG rno:00010 NCBI chr 3:161,930,256...161,936,205
Ensembl chr 3:161,930,256...161,936,191
JBrowse link
G Pck2 phosphoenolpyruvate carboxykinase 2 (mitochondrial) IEA KEGG rno:00010 NCBI chr15:29,027,891...29,036,729
Ensembl chr15:29,027,894...29,037,283
JBrowse link
G Pdha1 pyruvate dehydrogenase E1 subunit alpha 1 IEA KEGG rno:00010 NCBI chr  X:34,700,481...34,714,309
Ensembl chr  X:34,700,409...34,714,311
JBrowse link
G Pdha2 pyruvate dehydrogenase E1 subunit alpha 2 IEA KEGG rno:00010 NCBI chr 2:229,872,300...229,873,848 JBrowse link
G Pdhb pyruvate dehydrogenase E1 subunit beta IEA KEGG rno:00010 NCBI chr15:16,752,561...16,758,503
Ensembl chr15:16,750,980...16,758,500
JBrowse link
G Pfkfb1 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 1 TAS RGD PMID:15170386 RGD:2302793 NCBI chr  X:19,508,522...19,562,165
Ensembl chr  X:19,508,546...19,562,182
JBrowse link
G Pfkfb2 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2 TAS RGD PMID:15170386 RGD:2302793 NCBI chr13:42,147,473...42,174,699
Ensembl chr13:42,147,478...42,174,699
JBrowse link
G Pfkfb3 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 TAS RGD PMID:15170386 RGD:2302793 NCBI chr17:66,983,629...67,064,702
Ensembl chr17:66,983,686...67,063,125
JBrowse link
G Pfkfb4 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 4 TAS RGD PMID:15170386 RGD:2302793 NCBI chr 8:109,643,558...109,687,006
Ensembl chr 8:109,643,937...109,685,634
JBrowse link
G Pfkl phosphofructokinase, liver type TAS
IDA
IEA
KEGG
RGD
PMID:2931076 PMID:4273555 PMID:4353083 rno:00010, RGD:2302736, RGD:2302790, RGD:2302851 NCBI chr20:10,664,285...10,686,324
Ensembl chr20:10,664,272...10,686,315
JBrowse link
G Pfkm phosphofructokinase, muscle TAS
IEA
ISO
KEGG
SMPDB
RGD
PMID:2931076 SMP:00040 rno:00010, RGD:2302736 NCBI chr 7:129,221,679...129,259,192
Ensembl chr 7:129,221,653...129,259,192
JBrowse link
G Pfkp phosphofructokinase, platelet TAS
IEA
KEGG
RGD
PMID:2931076 rno:00010, RGD:2302736 NCBI chr17:63,729,743...63,794,026
Ensembl chr17:63,729,780...63,794,018
JBrowse link
G Pgam1 phosphoglycerate mutase 1 ISO
IEA
KEGG
SMPDB
RGD
PMID:18092946 SMP:00040 rno:00010, RGD:2302794 NCBI chr 1:240,723,832...240,731,443
Ensembl chr 1:240,723,920...240,738,452
JBrowse link
G Pgam2 phosphoglycerate mutase 2 ISO
IEA
KEGG
SMPDB
RGD
PMID:18092946 SMP:00040 rno:00010, RGD:2302794 NCBI chr14:80,681,796...80,683,907
Ensembl chr14:80,681,776...80,683,940
JBrowse link
G Pgk1 phosphoglycerate kinase 1 IDA
IMP
IEA
KEGG
RGD
PMID:6405813 PMID:3091090 rno:00010, RGD:2302859, RGD:2302860 NCBI chr  X:71,271,454...71,287,429
Ensembl chr  X:71,271,440...71,287,418
JBrowse link
G Pgk1l1 phosphoglycerate kinase 1 like 1 IEA KEGG rno:00010 NCBI chr 2:42,754,605...42,755,929
Ensembl chr 2:42,754,639...42,755,856
JBrowse link
G Pgk2 phosphoglycerate kinase 2 IEA KEGG rno:00010 NCBI chr 9:20,480,367...20,481,933
Ensembl chr 9:20,480,203...20,571,481
JBrowse link
G Pgm1 phosphoglucomutase 1 IEA KEGG rno:00010 NCBI chr 5:114,595,298...114,654,728
Ensembl chr 5:114,595,293...114,654,728
JBrowse link
G Pklr pyruvate kinase L/R IDA
IEA
ISO
KEGG
SMPDB
RGD
PMID:4273555 PMID:4353083 SMP:00040 rno:00010, RGD:2302790, RGD:2302851 NCBI chr 2:174,543,008...174,551,863
Ensembl chr 2:174,543,039...174,551,870
JBrowse link
G Pkm pyruvate kinase M1/2 IDA RGD PMID:4273555 RGD:2302790 NCBI chr 8:60,057,629...60,079,600
Ensembl chr 8:60,057,402...60,079,599
JBrowse link
G Slc2a2 solute carrier family 2 member 2 ISO SMPDB SMP:00040 NCBI chr 2:111,609,798...111,639,930
Ensembl chr 2:111,611,774...111,639,933
JBrowse link
G Tpi1 triosephosphate isomerase 1 IEA
ISO
KEGG
SMPDB
SMP:00040 rno:00010 NCBI chr 4:157,615,283...157,618,813
Ensembl chr 4:157,615,386...157,619,541
JBrowse link
G Tpi1l2 triosephosphate isomerase 1 like 2 IEA KEGG rno:00010 NCBI chr17:27,101,431...27,102,823
Ensembl chr17:27,101,431...27,102,809
JBrowse link

Additional Elements in Pathway:

(includes Gene Groups, Small Molecules, Other Pathways..etc.)
Object TypePathway ObjectPathway Object Description
Functional ClassPfkfb members (kinase)members of the bifunctional elzyme that catalyzes the synthesis and degradation of F2,6P
Functional ClassPfkfb members (phosphatase)members of the bifunctional elzyme that catalyzes the synthesis and degradation of F2,6P
Functional Classaldolasesthe aldolase isozymes
Functional Classenolasesthe enolase isozymes

Pathway Gene Annotations

Disease Annotations Associated with Genes in the glycolysis pathway
Disease TermsGene Symbols
Acute Alcohol SensitivityAldh2
Acute Coronary SyndromeEno1 , Gapdh , Ldhb
Acute Liver FailureFbp1 , Fbp2 , Ldha
Acute Lung InjuryPfkfb3
acute lymphoblastic leukemiaGpi , Hk1
acute myeloid leukemiaEno2 , Gpi
adenocarcinomaEno1 , Pgam1
adult-onset autosomal dominant demyelinating leukodystrophyAldh7a1
Aicardi-Goutieres Syndrome 1Pfkfb4
Aicardi-Goutieres Syndrome 3Aldh3b1
alcohol dependenceAdh4 , Aldh2
alcohol use disorderAdh5 , Aldh2
alcohol-induced mental disorderAldh2
Alcoholic Fatty LiverAldh2
alcoholic liver cirrhosisAldh2
Alcoholic Liver DiseasesAldh2
Alzheimer's diseaseAldh2 , Eno1 , Gapdh , Gapdhs , Pck1 , Tpi1
AMED syndromeAdh5 , Aldh2
anemiaHk1
Animal Disease ModelsEno1 , Gapdh , Gpi , Hk1 , Hk2 , Ldha , Tpi1
Animal Mammary NeoplasmsEno1 , Pgam1 , Pkm
aortic valve stenosisEno3
Arsenic PoisoningPfkfb3
arteriosclerosisAldh3a1
asthmaAdh5 , Aldh2
ataxia telangiectasiaDlat
AtrophyEno2
autism spectrum disorderAdh4 , Adh5 , Adh6 , Akr1a1 , Aldh1a1 , Aldh1a3 , Aldh2 , Aldh3a1 , Aldh3a2 , Aldh3b1 , Aldoa , Aldoart2 , Hk1
autistic disorderAldh1a3 , Aldh3a1 , Aldh3a2 , Aldoa , Aldoart2 , Pdha1 , Pfkfb1 , Pfkfb2 , Pfkl , Pgk1
autoimmune disease of the nervous systemAldoc
autoimmune hepatitisAldob
autoimmune polyendocrine syndrome type 1Pfkl
azoospermiaPdha2
Baker-Winegrad DiseaseFbp1
Bardet-Biedl syndromeAdpgk
benign neonatal seizuresAldh7a1
BH4-deficient hyperphenylalaninemia ADlat
Binge DrinkingAdh4
Bloom syndromeAdpgk , Ldhal6b , Pkm
bone diseaseAldh7a1
borna diseaseAldoc
brain diseaseEno2
brain gliomaGapdh
brain infarctionAldh2
Brain-Lung-Thyroid SyndromePck2
breast cancerAkr1a1
breast carcinomaEno2
Breast NeoplasmsAldoa , Eno1 , Gpi , Ldhal6b , Ldhb , Slc2a2
Brugada syndrome 5Gapdhs
Brugada syndrome 8Adpgk
buphthalmosGalm
BurnsPklr
carbohydrate metabolic disorderTpi1
CarcinogenesisAkr1a1
Carcinoid TumorEno2
carcinomaEno1 , Pgam1 , Pkm
cardiomyopathyLdha
Carney-Stratakis syndromeDlat
cataractAldh3a1
cataract 9 multiple typesPfkl
celiac diseasePck1
Charcot-Marie-Tooth disease dominant intermediate CAkr1a1
Charcot-Marie-Tooth disease type 2Pklr
Charcot-Marie-Tooth disease type 4GHk1
Chemical and Drug Induced Liver InjuryAkr1a1 , Aldh2 , Aldh9a1 , Aldob , Dlat , Eno1 , G6pc1 , Pgm1
Childhood-Onset Remitting LeukodystrophyFbp2
cholestasisAdh5 , Aldh1b1
Chromosome 11, Partial Trisomy 11qDlat
chromosome 15q26-qter deletion syndromeAldh1a3
chromosome 16p11.2 deletion syndrome, 593-kbAldoa , Aldoart2
chromosome 16p11.2 duplication syndromeAldoa , Aldoart2
chromosome 1p36 deletion syndromeEno1
Chromosome 5, Trisomy 5qHk3
Chronic Intermittent HypoxiaHk1 , Hk2 , Pck1
Cluster HeadacheAdh4
Coffin-Lowry syndromePdha1
colobomaAldh7a1
Colonic NeoplasmsAldh1b1 , Fbp1
colorectal cancerAdpgk , Hk1 , Ldhal6b , Pkm
Colorectal NeoplasmsAldh2 , Gapdh , Pgm1
common variable immunodeficiency 2Aldh3a2
common variable immunodeficiency 7Pfkfb2
congenital disorder of glycosylationPgm1
congenital disorder of glycosylation IlDlat
congenital disorder of glycosylation ItPgm1
congenital hemolytic anemiaGpi
Congenital HyperinsulinismGck
Congenital Infantile Lactic Acidosis due to LAD DeficiencyDld
congenital myasthenic syndrome 4AEno3
congenital nonspherocytic hemolytic anemiaGpi , Hk1 , Pklr , Tpi1
congestive heart failurePck1
Corneal InjuriesAldh3a1
Cornelia de Lange syndrome 2Pfkfb1
coronary artery diseaseGck
coronin-1A deficiencyAldoa , Aldoart2
COVID-19Aldh9a1 , Eno1 , Gapdh , Hk1 , Ldha , Pck2 , Pkm , Tpi1
Craniosynostosis Syndrome, Autosomal RecessivePgm1
Creutzfeldt-Jakob diseaseAldh1a1
cystadenomaAldoa , Aldoart2
developmental and epileptic encephalopathyAkr1a1
developmental and epileptic encephalopathy 1Aldh7a1
developmental and epileptic encephalopathy 13Aldh7a1
developmental and epileptic encephalopathy 2Pdha1
developmental and epileptic encephalopathy 21Eno2 , Tpi1
developmental and epileptic encephalopathy 30Pfkl
Diabetes ComplicationsAldh2
diabetes mellitusAldob , Gck , Slc2a2
diabetic neuropathyAldh2
diabetic retinopathyGapdh
dilated cardiomyopathy 1IIDlat
dilated cardiomyopathy 1OLdhb
Dimauro DiseasePgam2
Disease ProgressionAldh7a1 , Pdha1
ductal carcinoma in situLdhb
DwarfismG6pc1
dystoniaGapdhs
early infantile epileptic encephalopathyAkr1a1
early-onset vitamin B6-dependent epilepsy 4Aldh7a1
Ehlers-Danlos syndrome dermatosparaxis typeHk3
Ehlers-Danlos syndrome spondylodysplastic type 2Hk3
Elevated Adenosine Triphosphate of ErythrocytesPklr
endometrial cancerPgm1
Endometrioid CarcinomasEno2
EndotoxemiaAldoa , Pck1 , Pck2
epilepsyAldh7a1 , Gapdh , Hk1 , Pdha1 , Pdhb
Episodic Kinesigenic DyskinesiaAldoa
episodic kinesigenic dyskinesia 1Aldoa
esophageal cancerAldh2
Esophageal NeoplasmsAdh7 , Aldh2 , Eno1 , Gapdh
esophagus squamous cell carcinomaAldh2 , Tpi1
Experimental ArthritisGpi
Experimental Diabetes MellitusAldob , Eno2 , G6pc1 , Gapdh , Gck , Hk1 , Pck1 , Pfkm , Pklr , Slc2a2 , Tpi1
Experimental Liver CirrhosisAdh4 , Aldh1a1 , Aldh1b1 , Aldh2 , G6pc1 , Gck , Ldhb , Pck1 , Pck2 , Pfkp , Pklr
Experimental Liver NeoplasmsEno2
Experimental Mammary NeoplasmsEno1 , Pgam1 , Pkm
Experimental MelanomaAcss1 , Acss2
Experimental NeoplasmsEno2 , Ldha
extrinsic cardiomyopathyPfkfb3
familial adenomatous polyposis 1Aldh7a1
familial erythrocytosis 8Bpgm
familial hyperinsulinemic hypoglycemia 3Gck
Fanconi syndromeLdha , Slc2a2
Fetal Growth RetardationG6pc1 , Pck1 , Slc2a2
FlushingAldh2
focal segmental glomerulosclerosis 6Ldhal6b
fructose-1,6-bisphosphatase deficiencyAldob , Fbp1
fundus dystrophyHk1
Galactosemia IVGalm
gastrinomaSlc2a2
gastrointestinal stromal tumorAldh9a1 , Pfkfb2 , Pklr
Gaucher's diseasePklr
Generalized EpilepsyPgk1
genetic diseaseAldh1a3 , Aldh1b1 , Aldh3a2 , Aldh7a1 , Aldoa , Aldoart2 , Aldob , Dlat , Dld , Eno3 , Fbp1 , G6pc1 , Galm , Gck , Gpi , Hk1 , Ldha , Pck1 , Pdha1 , Pdhb , Pfkm , Pgam2 , Pgk1 , Pgm1 , Pklr , Slc2a2 , Tpi1
Genetic Predisposition to DiseaseAldh2
gestational diabetesG6pc1 , Gck
GlucagonomaSlc2a2
glycogen storage diseaseG6pc1 , Pfkm , Slc2a2
glycogen storage disease IG6pc1
glycogen storage disease IaG6pc1
Glycogen Storage Disease IAG6pc1
glycogen storage disease IVPfkm
glycogen storage disease IXAPdha1
glycogen storage disease VIIPfkm
Glycogen Storage Disease XILdha
Glycogen Storage Disease XIIAldoa , Aldoart2
Glycogen Storage Disease XIIIEno3
heart diseaseAldh2
Heart InjuriesAldh2
hemolytic anemiaGpi , Pgk1 , Pklr , Tpi1
Hemorrhagic ShockAldh1a7
hepatocellular carcinomaAdh4 , Akr1a1 , Aldh2 , Aldh7a1 , Aldoc , Eno1 , Fbp1 , G6pc1 , Gapdh , Pck1 , Pgk1 , Pkm , Slc2a2
HepatomegalyAldh1b1
hereditary breast ovarian cancer syndromeEno2
hereditary fructose intolerance syndromeAldoa , Aldob
Hereditary Neoplastic SyndromesAldh7a1
hereditary spastic paraplegia 75Gapdhs , Gpi
hereditary spherocytosisGpi
heroin dependenceAldh2
Hexokinase Deficiency Hemolytic AnemiaHk1
hiatus herniaFbp1 , Fbp2
homocystinuriaPfkl
Huntington's diseaseGapdh
hydrocephalusAldh7a1
hyperglycemiaGck , Ldha , Pck1 , Pklr
hyperinsulinemic hypoglycemiaGck
hyperinsulinismGck , Pfkfb1 , Pklr
Hyperphosphatemic Familial Tumoral Calcinosis 1Eno2 , Gapdh , Tpi1
hypertensionAldh2 , Eno1 , Eno2 , Gck , Hk2 , Ldha , Pkm
HypertriglyceridemiaPklr
hypertrophic cardiomyopathy 12Ldha , Ldhc
hypoglycemiaG6pc1 , Gck
Hypokalemic Periodic Paralysis, Type 1Pfkfb2
hypoparathyroidism-deafness-renal disease syndromePfkfb3
HypothermiaAcss1
HypoxiaAldob , Gapdh , Pck2
immunodeficiency 42Pklr
InflammationAcss2
inflammatory bowel diseasePfkfb2
inherited metabolic disorderLdhb , Tpi1
Insulin ResistanceAldh2 , Gck , Pklr
insulinomaSlc2a2
intellectual disabilityAldh3b1 , Aldh7a1 , Aldob , Dlat , Gpi , Ldha , Ldhc , Pgm1
isolated microphthalmia 8Aldh1a3
Joubert syndrome 1Aldh3a2
keratoconusAldh3a1
Kidney NeoplasmsEno2
Kidney Reperfusion InjuryAkr1a1 , Aldh2
Klippel-Feil syndrome 3Eno2 , Tpi1
Lactate Dehydrogenase B DeficiencyLdhb
lactic acidosisPdha1
Laryngeal NeoplasmsAdh7
Leigh diseaseDld
Leigh Syndrome, X-LinkedPdha1
LeukoencephalopathiesAldh7a1
Lewy body dementiaEno2
lissencephaly 5Dld
liver benign neoplasmAldob
liver cancerAldh2
liver diseaseAldh1a1 , Aldh2 , Eno3 , Hk3
Liver FailureG6pc1
Liver InjuryGck
Liver Reperfusion InjuryAldh2
long QT syndromeAcss2 , Hk3
Long-Chain 3-hydroxyacyl-CoA Dehydrogenase DeficiencyAldob
lung adenocarcinomaAkr1a1 , Aldoa , Eno1 , Gapdh , Gpi , Hk1 , Hk2 , Ldha , Tpi1
lung diseaseLdhc
lung non-small cell carcinomaEno1 , Eno2 , Pgam1
lymphangioleiomyomatosisAcss2 , Gapdh , Pkm
lymphoproliferative syndrome 2Eno2 , Gapdh , Tpi1
Lynch syndromeGalm
lysinuric protein intolerancePck2
macular degenerationHk1
malariaPklr
male infertilityAldh2 , Eno1 , Ldhc
maple syrup urine diseaseDld
Marfanoid Mental Retardation Syndrome, AutosomalHk3
maturity-onset diabetes of the youngGck
maturity-onset diabetes of the young type 1Gck , Slc2a2
maturity-onset diabetes of the young type 2Gck
maturity-onset diabetes of the young type 3Gck
Meckel Syndrome 9Aldh3a1 , Aldh3a2
melanomaAldh1a1 , Aldh1a3
MelanosisAldh2
Menkes diseasePgk1
Mental Retardation, Autosomal Recessive 42Gpi
metabolic dysfunction-associated steatohepatitisPck1
metabolic dysfunction-associated steatotic liver diseaseAdh4 , Aldh1a1 , Aldh1b1 , Aldh2 , G6pc1 , Pklr
Metabolic SyndromeAldoa , G6pc1 , Gck , Pck1
MHC class II deficiencyPklr
microphthalmiaAldh1a3
middle cerebral artery infarctionGapdh
migraine without auraEno2
mitochondrial metabolism diseasePdha1
morbid obesityAcss2
Mouth NeoplasmsAdh7 , Eno1 , Gapdh , Pgam1 , Tpi1
multiple myelomaHk1
Multiple TraumaEno2
myocardial infarctionAldh2 , Ldha
Myocardial IschemiaAldh2 , Aldoa , Dlat , Hk1 , Hk2 , Pdha1 , Pfkfb3 , Pfkm , Pgm1
Myocardial Reperfusion InjuryAldh2 , Gapdh
myoglobinuriaLdha , Pgam2
Nance-Horan syndromePdha1
NecrosisGapdh
neonatal diabetesGck
Neoplasm InvasivenessAldoa , Eno1 , Ldhb , Pkm
Neoplasm MetastasisAldoa , Gpi
Neoplastic Cell TransformationAldh1a1 , Eno2
Nerve DegenerationPank1
Nerve Tissue NeoplasmsEno2
Nervous System MalformationsAldh7a1
neural tube defectSlc2a2
NEURODEVELOPMENTAL DISORDER WITH VISUAL DEFECTS AND BRAIN ANOMALIESHk1
Neurodevelopmental DisordersAldh1a3 , Aldh7a1 , Aldoa , Eno1 , Hk1 , Pdha1 , Pfkl
neuroendocrine carcinomaEno2
neuromuscular diseaseGpi , Tpi1
Neuromuscular ManifestationsTpi1
Nonspherocytic Hemolytic Anemia due to Glucose Phosphate Isomerase DeficiencyGpi
Nonspherocytic Hemolytic Anemia, due to Hexokinase DeficiencyHk1
obesityGapdh , Gck , Hk1 , Hk2 , Pck1 , Pfkfb3 , Pklr
occupational dermatitisAldh2
ocular hypertensionTpi1
oral squamous cell carcinomaGapdh
orofacial cleftAcss2
osteoarthritisEno1 , Gapdh , Pdha1
osteoporosisEno1 , Gapdh , Pkm , Tpi1
pancreatic cancerAldh1a1 , Aldh2 , Ldha
pancreatic ductal carcinomaSlc2a2
parathyroid carcinomaAldh9a1 , Pfkfb2 , Pklr
Parkinson's diseaseAdh7 , Aldh2 , Eno2 , Fbp1
ParkinsonismAldh1a1 , Eno2 , Gapdh
perinatal necrotizing enterocolitisAkr1a1 , Aldh2 , Eno1
peritonitisAldob
permanent neonatal diabetes mellitusGck
Permanent Neonatal Diabetes Mellitus 1Gck
peroxisome biogenesis disorder 2BEno2 , Gapdh , Tpi1
peroxisome biogenesis disorder 3BPfkm
Pharyngeal NeoplasmsAdh7
Phosphoenolpyruvate Carboxykinase DeficiencyPck1
Phosphoenolpyruvate Carboxykinase Deficiency, CytosolicPck1
Phosphoenolpyruvate Carboxykinase Deficiency, MitochondrialPck2
phosphoglycerate kinase 1 deficiencyPgk1
pleomorphic xanthoastrocytomaBpgm , Dld , Gck , Pgam2
Potocki-Lupski syndromeAldh3a1 , Aldh3a2
pre-malignant neoplasmAldh2
Pregnancy in DiabeticsGapdh
Prenatal Exposure Delayed EffectsAdh4
Primary Autosomal Recessive Microcephaly 21Gapdh
primary ciliary dyskinesiaPfkl
Progressive Microcephaly with Seizures and Cerebral and Cerebellar AtrophyPfkfb4
progressive myoclonus epilepsyPfkl
progressive myoclonus epilepsy 7Ldha , Ldhc
prostate cancerAldh9a1 , Dlat , Eno2 , Gapdhs
Prostatic NeoplasmsLdhb , Pdha1 , Pgam2
pulmonary hypertensionAdh5 , Hk1
pyridoxine-dependent epilepsyAldh7a1
pyruvate decarboxylase deficiencyDld , Pdha1 , Pdhb
Pyruvate Dehydrogenase E1 Alpha DeficiencyPdha1
Pyruvate Dehydrogenase E1-Beta DeficiencyPdhb
Pyruvate Dehydrogenase E2 DeficiencyDlat
Pyruvate Dehydrogenase Phosphatase DeficiencyPdhb
pyruvate kinase deficiency of red cellsPklr
Pyruvate Metabolism, Inborn ErrorsPdha1
RASopathyGalm
Recurrent Infections, with Encephalopathy, Hepatic Dysfunction, and Cardiovascular MalformationsAldh3b1
renal cell carcinomaAldh1a1 , Ldhb , Pdhb , Pgk1
Reperfusion InjuryAldoa , Eno2 , Pklr
retinitisHk1
retinitis pigmentosaHk1
retinitis pigmentosa 27Pck2
Retinitis Pigmentosa 79Hk1
RhabdomyolysisPfkm , Pgam2
rheumatic heart diseaseGapdh
rheumatoid arthritisEno1
schizophreniaAdpgk , Aldoa , Aldoart2 , Fbp1 , Pfkfb3 , Pfkp
SepsisAldh2
severe congenital neutropenia 3Pklr
severe congenital neutropenia 5Pklr
sickle cell anemiaHk1
Sjogren-Larsson syndromeAldh3a2
skin diseasePfkfb3
Sleep DeprivationDlat
Sotos syndromeHk3
spastic ataxia 2Eno3
Specific Granule DeficiencyPck2
spermatogenic failure 1Pdha2
Spermatogenic Failure 70Pdha2
Spinal Cord InjuriesEno2 , Gapdh
Spinal Cord Reperfusion InjuryGapdh
spondylocostal dysostosis 5Aldoa , Aldoart2
squamous cell carcinomaEno1 , Gapdh , Pgam1 , Tpi1
steatotic liver diseaseG6pc1 , Gck , Slc2a2
Stomach NeoplasmsAldh1a3 , Aldh7a1 , Aldob , Eno1 , Fbp1 , Pdha1 , Pgam1
StrokeAldoc
Subacute Necrotizing Encephalopathy of Leigh, InfantileDld
sudden infant death syndromePdha1
syndromic microphthalmia 5Pfkp
syndromic microphthalmia 9Aldh1a3
syndromic X-linked intellectual disability Lubs typePdha1 , Pfkfb1 , Pgk1
Tay-Sachs diseaseAdpgk , Pkm
Temtamy syndromeEno2 , Gapdh , Tpi1
teratomaPgm1
toxic shock syndromeEno2
transient neonatal diabetes mellitusGck
triosephosphate isomerase deficiencyTpi1
type 1 diabetes mellitusAldh2
type 2 diabetes mellitusAldh2 , Aldob , G6pc1 , Gapdh , Gck , Hk1 , Hk2 , Pck1 , Pklr , Slc2a2
urinary bladder cancerEno2 , Hk1
Urologic NeoplasmsEno2
vascular diseaseAldh2
Ventricular DysfunctionAldh2
VentriculomegalyAldh7a1
Viral BronchiolitisGapdh
visual epilepsyAldh7a1 , Eno2
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasiaPgk1
Young SyndromePgk1
Pathway Annotations Associated with Genes in the glycolysis pathway
Pathway TermsGene Symbols
2-aminoadipic 2-oxoadipic aciduria pathwayAldh7a1 , Dld
3-hydroxy-3-methylglutaryl-CoA lyase deficiency pathwayAldh2 , Dld
3-hydroxyisobutyric aciduria pathwayAldh2 , Dld
3-methylcrotonyl CoA carboxylase 1 deficiency pathwayAldh2 , Dld
3-methylglutaconic aciduria type 1 pathwayAldh2 , Dld
3-methylglutaconic aciduria type 3 pathwayAldh2 , Dld
alkaptonuria pathwayAldh3a1
altered galactose metabolic pathwayG6pc1 , Hk2
Alzheimer's disease pathwayGapdh , Gapdh-ps118 , Gapdhl10 , Gapdhl3 , Gapdhl9
amino sugar metabolic pathwayGck , Gpi , Hk1 , Hk2 , Hk3 , Pgm1
arginine and proline metabolic pathwayAldh1a1 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a2 , Aldh7a1 , Aldh9a1
ascorbate and aldarate metabolic pathwayAldh1a1 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a2 , Aldh7a1 , Aldh9a1
beta-alanine metabolic pathwayAldh1a1 , Aldh1a3 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a1 , Aldh3a2 , Aldh3b1 , Aldh7a1 , Aldh9a1
butanoate metabolic pathwayPdha1 , Pdha2 , Pdhb
butirosin and neomycin biosynthetic pathwayGck , Hk1 , Hk2 , Hk3
carnitine biosynthetic pathwayAldh9a1
carnosinemia pathwayAldh2
choline metabolic pathwayAldh7a1
citric acid cycle pathwayDlat , Dld , Pck1 , Pck2 , Pdha1 , Pdha2 , Pdhb
congenital sucrase-isomaltase deficiency pathwayGck , Gpi , Hk2 , Pgm1
cyclophosphamide pharmacodynamics pathwayAldh1a1 , Aldh3a1
cyclophosphamide pharmacokinetics pathwayAldh1a1 , Aldh3a1
cysteine and methionine metabolic pathwayLdha , Ldhal1 , Ldhal6b , Ldhb , Ldhc
D-glycericacidemia pathwayAldh3a1
dihydropyrimidine dehydrogenase deficiency pathwayAldh2 , Dld
dimethylglycine dehydrogenase deficiency pathwayAldh2 , Dld
disulfiram pharmacodynamics pathwayAcss1 , Acss2 , Aldh1b1 , Aldh2 , Aldh3a1
dopamine beta-hydroxylase deficiency pathwayAldh3a1
doxorubicin pharmacokinetics pathwayAkr1a1
eicosanoid signaling pathway via peroxisome proliferator-activated receptor gammaPck1 , Pck2
electron transport chain pathwayGapdh
facilitative sugar transporter mediated glucose transport pathwaySlc2a2
familial lipoprotein lipase deficiency pathwayAldh3a1
Fanconi syndrome pathwayAldoa , Aldoart2 , Bpgm , Eno1 , G6pc1 , Galm , Gapdh , Gpi , Hk2 , Pank1 , Pfkm , Pgam1 , Pgam2 , Pklr , Slc2a2 , Tpi1
fatty acid beta degradation pathwayAcss1 , Acss2
fatty acid metabolic pathwayAdh4 , Adh5 , Adh6 , Adh7 , Aldh1a1 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a2 , Aldh7a1 , Aldh9a1
felbamate pharmacokinetics pathwayAldh3a1
folate cycle metabolic pathwayDld
forkhead class A signaling pathwayAldob , G6pc1 , Gck , Pck1 , Pklr , Slc2a2
french type sialuria pathwayHk1
fructose and mannose metabolic pathwayAldoa , Aldoart2 , Aldob , Aldoc , Fbp1 , Fbp2 , Hk1 , Hk2 , Hk3 , Pfkfb1 , Pfkfb2 , Pfkfb3 , Pfkfb4 , Pfkl , Pfkm , Pfkp , Tpi1 , Tpi1l2
fructose-1,6-bisphosphatase deficiency pathwayAldoa , Aldoart2 , Bpgm , Eno1 , Fbp1 , G6pc1 , Galm , Gapdh , Gpi , Hk2 , Pank1 , Pck1 , Pgam1 , Pgam2 , Pgm1 , Slc2a2 , Tpi1
fructosuria pathwayAldoa , Aldoart2 , Aldob , Fbp1 , Hk1 , Pfkfb1 , Pfkl , Tpi1
fumaric aciduria pathwayDlat , Dld , Pdha1 , Pdhb
GABA aminotransferase deficiency pathwayAldh2
galactokinase deficiency pathwayGck , Pgm1
galactose metabolic pathwayG6pc1 , Gck , Hk1 , Hk2 , Hk3 , Pfkl , Pfkm , Pfkp , Pgm1
galactosemia pathwayG6pc1 , Gck , Hk1 , Pgm1
GALE deficiency pathwayGck , Pgm1
gliclazide pharmacodynamics pathwaySlc2a2
gluconeogenesis pathwayAcss1 , Acss2 , Adh4 , Adh5 , Adh6 , Adh7 , Adpgk , Akr1a1 , Aldh1a1 , Aldh1a3 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a1 , Aldh3a2 , Aldh3b1 , Aldh7a1 , Aldh9a1 , Aldoa , Aldoart2 , Aldob , Aldoc , Bpgm , Dlat , Dld , Eno1 , Eno2 , Eno3 , Fbp1 , Fbp2 , G6pc1 , Galm , Gapdh , Gapdh-ps118 , Gapdhl10 , Gapdhl3 , Gapdhl9 , Gapdhs , Gck , Gpi , Hk1 , Hk2 , Hk3 , Ldha , Ldhal1 , Ldhal6b , Ldhb , Ldhc , Pank1 , Pck1 , Pck2 , Pdha1 , Pdha2 , Pdhb , Pfkfb1 , Pfkl , Pfkm , Pfkp , Pgam1 , Pgam2 , Pgk1 , Pgk1l1 , Pgk2 , Pgm1 , Pklr , Slc2a2 , Tpi1 , Tpi1l2
Glut1 deficiency syndrome pathwayG6pc1
glutaric aciduria type I pathwayAldh7a1 , Dld
glyburide pharmacodynamics pathwaySlc2a2
glycerol kinase deficiency pathwayAldh3a1
glycerolipid metabolic pathwayAkr1a1 , Aldh1a1 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a1 , Aldh3a2 , Aldh7a1 , Aldh9a1
glycine, serine and threonine metabolic pathwayAldh7a1 , Dld
glycogen biosynthetic pathwayGck , Pgm1
glycogen degradation pathwayPgm1
glycogen metabolic pathwayGck
glycogen storage disease type Ia pathwayAldoa , Aldoart2 , Bpgm , Eno1 , Fbp1 , G6pc1 , Galm , Gapdh , Gpi , Hk2 , Pank1 , Pck1 , Pgam1 , Pgam2 , Pgm1 , Slc2a2 , Tpi1
glycogen storage disease type Ib pathwayAldoa , Aldoart2 , Bpgm , Eno1 , Fbp1 , G6pc1 , Galm , Gapdh , Gpi , Hk2 , Pank1 , Pck1 , Pgam1 , Pgam2 , Pgm1 , Slc2a2 , Tpi1
glycogen storage disease type III pathwayGck , Gpi , Hk2 , Pgm1
glycogen storage disease type IV pathwayGck , Gpi , Hk2 , Pgm1
glycogen storage disease type VI pathwayGck , Gpi , Hk2 , Pgm1
glycogen storage disease type VII pathwayAldoa , Aldoart2 , Bpgm , Eno1 , G6pc1 , Galm , Gapdh , Gpi , Hk2 , Pank1 , Pfkm , Pgam1 , Pgam2 , Pklr , Slc2a2 , Tpi1
glycolysis pathwayAcss1 , Acss2 , Adh4 , Adh5 , Adh6 , Adh7 , Adpgk , Akr1a1 , Aldh1a1 , Aldh1a3 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a1 , Aldh3a2 , Aldh3b1 , Aldh7a1 , Aldh9a1 , Aldoa , Aldoart2 , Aldob , Aldoc , Bpgm , Dlat , Dld , Eno1 , Eno2 , Eno3 , Fbp1 , Fbp2 , G6pc1 , Galm , Gapdh , Gapdh-ps118 , Gapdhl10 , Gapdhl3 , Gapdhl9 , Gapdhs , Gck , Gpi , Hk1 , Hk2 , Hk3 , Ldha , Ldhal1 , Ldhal6b , Ldhb , Ldhc , Pank1 , Pck1 , Pck2 , Pdha1 , Pdha2 , Pdhb , Pfkfb1 , Pfkfb2 , Pfkfb3 , Pfkfb4 , Pfkl , Pfkm , Pfkp , Pgam1 , Pgam2 , Pgk1 , Pgk1l1 , Pgk2 , Pgm1 , Pklr , Pkm , Slc2a2 , Tpi1 , Tpi1l2
glycolysis/gluconeogenesis pathwayAcss1 , Acss2 , Adh4 , Adh5 , Adh6 , Adh7 , Adpgk , Akr1a1 , Aldh1a1 , Aldh1a3 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a1 , Aldh3a2 , Aldh3b1 , Aldh7a1 , Aldh9a1 , Aldoa , Aldob , Aldoc , Bpgm , Dlat , Dld , Eno1 , Eno2 , Eno3 , Fbp1 , Fbp2 , G6pc1 , Galm , Gapdh , Gapdh-ps118 , Gapdhl10 , Gapdhl3 , Gapdhl9 , Gapdhs , Gck , Gpi , Hk1 , Hk2 , Hk3 , Ldha , Ldhal1 , Ldhal6b , Ldhb , Ldhc , Pck1 , Pck2 , Pdha1 , Pdha2 , Pdhb , Pfkl , Pfkm , Pfkp , Pgam1 , Pgam2 , Pgk1 , Pgk1l1 , Pgk2 , Pgm1 , Pklr , Tpi1 , Tpi1l2
hawkinsinuria pathwayAldh3a1
hereditary fructose intolerance syndrome pathwayAldoa , Aldoart2 , Aldob , Fbp1 , Hk1 , Pfkfb1 , Pfkl , Tpi1
hexosamine biosynthetic pathwayGpi
histidine metabolic pathwayAldh1a1 , Aldh1a3 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a1 , Aldh3a2 , Aldh3b1 , Aldh7a1 , Aldh9a1
histidinemia pathwayAldh2 , Aldh3a1
hyperlysinemia pathwayAldh7a1 , Dld
hypoxia inducible factor pathwayAldoa , Aldoart2 , Eno1 , Gck , Hk1 , Hk2 , Ldha , Pfkfb3 , Pfkl , Pgk1 , Pgm1 , Pkm
ifosfamide pharmacodynamics pathwayAldh1a1 , Aldh3a1
ifosfamide pharmacokinetics pathwayAldh1a1 , Aldh3a1
inositol phosphate metabolic pathwayTpi1 , Tpi1l2
insulin secretion pathwayGck , Slc2a2
insulin signaling pathwayFbp1 , Fbp2 , G6pc1 , Gck , Hk1 , Hk2 , Hk3 , Pck1 , Pck2 , Pklr
isobutyryl-CoA dehydrogenase deficiency pathwayAldh2 , Dld
isovaleric acidemia pathwayAldh2 , Dld
lactose biosynthetic pathwayG6pc1
lactose degradation pathwaySlc2a2
lamivudine pharmacokinetics pathwayPgk1
Leigh disease pathwayAcss2 , Aldh2 , Dlat , Dld , Pck1 , Pdha1 , Pdhb , Pklr
lysine biosynthetic pathwayAldh7a1
lysine degradation pathwayAldh1a1 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a2 , Aldh7a1 , Aldh9a1 , Dld
malonic aciduria pathwayAcss1 , Dld , Ldhal6b
maple syrup urine disease pathwayAldh2 , Dld
maturity-onset diabetes of the young pathwayGck , Pklr , Slc2a2
methylmalonate semialdehyde dehydrogenase deficiency pathwayAldh2 , Dld
methylmalonic acidemia pathwayAldh2 , Dld
methylmalonic aciduria, cobalamin-related pathwayAcss1 , Dld , Ldhal6b
mitochondrial complex II deficiency pathwayDlat , Dld , Pdha1 , Pdhb
neviparine pharmacokinetics pathwayAldh1a1
nicotinamide adenine dinucleotide metabolic pathwayGapdh
nonketotic hyperglycinemia pathwayAldh2 , Dld
Notch signaling pathwayEno1
nucleotide sugar metabolic pathwayGck , Gpi , Hk1 , Hk2 , Hk3 , Pgm1
pantothenic acid metabolic pathwayPank1
pentose and glucuronate interconversion pathwayAldh1a1 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a2
pentose phosphate pathwayAldoa , Aldoart2 , Aldob , Aldoc , Fbp1 , Fbp2 , Gpi , Pfkl , Pfkm , Pfkp , Pgm1
phase I biotransformation pathway via cytochrome P450Adh4 , Adh5 , Adh6 , Adh7 , Aldh1a3 , Aldh3a1 , Aldh3b1
phenylalanine metabolic pathwayAldh1a3 , Aldh3a1 , Aldh3b1
phosphoenolpyruvate carboxykinase deficiency pathwayAldoa , Aldoart2 , Bpgm , Eno1 , Fbp1 , G6pc1 , Galm , Gapdh , Gpi , Hk2 , Pank1 , Pck1 , Pgam1 , Pgam2 , Pgm1 , Slc2a2 , Tpi1
phytanic acid degradation pathwayAldh3a2
potassium channel inhibitors pharmacodynamics pathwaySlc2a2
primary hyperoxaluria type 2 pathwayAcss2 , Aldh2 , Dlat , Dld , Pck1 , Pdha1 , Pdhb , Pklr
propanoate metabolic pathwayAcss1 , Acss2 , Aldh1a1 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a2 , Aldh7a1 , Aldh9a1 , Dld , Ldha , Ldhal1 , Ldhal6b , Ldhb , Ldhc
propionic acidemia pathwayAldh2 , Dld
prostaglandin biosynthetic pathwayAkr1a1
purine metabolic pathwayPgm1 , Pklr
pyruvate decarboxylase deficiency pathwayAcss2 , Aldh2 , Dlat , Dld , Pck1 , Pdha1 , Pdhb , Pklr
pyruvate dehydrogenase E1 deficiency pathwayAcss2 , Aldh2 , Dlat , Dld , Pck1 , Pdha1 , Pdhb , Pklr
pyruvate dehydrogenase E2 deficiency pathwayDlat , Dld , Pdha1 , Pdhb
pyruvate dehydrogenase E3 deficiency pathwayDlat , Dld , Pdha1 , Pdhb
pyruvate kinase deficiency of red cells pathwayAcss2 , Aldh2 , Dlat , Dld , Pck1 , Pdha1 , Pdhb , Pklr
pyruvate metabolic pathwayAcss1 , Acss2 , Aldh1a1 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a2 , Aldh7a1 , Aldh9a1 , Dlat , Dld , Ldha , Ldhal1 , Ldhal6b , Ldhb , Ldhc , Pck1 , Pck2 , Pdha1 , Pdha2 , Pdhb , Pklr , Pkm
Refsum disease pathwayAldh3a2
remethylation pathway of homocysteine metabolism - cobalamin independent, betaine dependentAldh7a1
retinoic acid metabolic pathwayAldh1a1 , Aldh1a3
retinol metabolic pathwayAdh4 , Adh5 , Adh6 , Adh7 , Aldh1a1
ribose 5-phosphate isomerase deficiency pathwayAldoa , Aldoart2 , Fbp1 , Gpi , Pfkl , Pgm1
RNA degradation pathwayEno1 , Eno2 , Eno3
saccharopinuria pathwayAldh7a1 , Dld
sarcosinemia pathwayAldh2 , Dld
sialic acid storage disease pathwayHk1
starch and sucrose metabolic pathwayG6pc1 , Gck , Gpi , Hk1 , Hk2 , Hk3 , Pgm1
Tay-Sachs disease pathwayHk1
transaldolase deficiency pathwayAldoa , Aldoart2 , Fbp1 , Gpi , Pfkl , Pgm1
trehalose degradation pathwayGck , Slc2a2
triosephosphate isomerase deficiency pathwayAldoa , Aldoart2 , Bpgm , Eno1 , Fbp1 , G6pc1 , Galm , Gapdh , Gpi , Hk2 , Pank1 , Pck1 , Pgam1 , Pgam2 , Pgm1 , Slc2a2 , Tpi1
tryptophan metabolic pathwayAldh1a1 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a2 , Aldh7a1 , Aldh9a1
type 2 diabetes mellitus pathwayGck , Hk1 , Hk2 , Hk3 , Pklr , Slc2a2
tyrosine metabolic pathwayAdh4 , Adh5 , Adh6 , Adh7 , Aldh1a3 , Aldh3a1 , Aldh3b1
tyrosinemia type I pathwayAldh3a1
valine, leucine and isoleucine biosynthetic pathwayPdha1 , Pdha2 , Pdhb
valine, leucine and isoleucine degradation pathwayAldh1a1 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a2 , Aldh7a1 , Aldh9a1 , Dld
vitamin A deficiency pathwayAldh1a1
Phenotype Annotations Associated with Genes in the glycolysis pathway

References Associated with the glycolysis pathway:

Ontology Path Diagram:

paths to the root
paths to the root

Import into Pathway Studio: