Glucose metabolism in triple-negative breast cancer cells

No Pathway Network information available for Glucose metabolism in triple-negative breast cancer cells

Pathways in the Glucose metabolism in triple-negative breast cancer cells SuperPath

Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways

Disorders associated with Glucose metabolism in triple-negative breast cancer cells SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Anemia, congenital, nonspherocytic hemolytic, 5EnrichmentHK13.23
2Stomatin-deficient cryohydrocytosis with neurologic defectsEnrichmentSLC2A13.23
3Erythrocyte lactate transporter defectEnrichmentSLC16A13.23
4Retinitis pigmentosa 79EnrichmentHK13.23
5Pyruvate dehydrogenase phosphatase deficiencyEnrichmentPDP13.23
6Neuropathy, hereditary motor and sensory, russe typeEnrichmentHK13.23
7Neurodevelopmental disorder with visual defects and brain anomaliesEnrichmentHK13.23
8Epilepsy, idiopathic generalized 12EnrichmentSLC2A13.23
9Epilepsy with myoclonic absencesEnrichmentSLC2A13.23
10Hereditary cryohydrocytosis with reduced stomatinEnrichmentSLC2A13.23
11Fanconi-bickel syndromeEnrichmentLDHA2.93
12Dystonia 9EnrichmentSLC2A12.93
13Glut1 deficiency syndrome 1EnrichmentSLC2A12.93
14Monocarboxylate transporter 1 deficiencyEnrichmentSLC16A12.93
15Glucose transporter type 1 deficiency syndromeEnrichmentSLC2A12.93
16Hyperinsulinemic hypoglycemia, familial, 7EnrichmentSLC16A12.93
17Ketoacidosis due to monocarboxylate transporter-1 deficiencyEnrichmentSLC16A12.93
18Glut1 deficiency syndrome 2EnrichmentSLC2A12.75
19Chromosome 17q23.1-q23.2 deletion syndromeEnrichmentSLC2A12.75
20Paroxysmal dystoniaEnrichmentSLC2A12.38
21Alternating hemiplegia of childhoodEnrichmentSLC2A12.33
22Myoclonic-atonic epilepsyEnrichmentSLC2A12.28
23Developmental and epileptic encephalopathy 1EnrichmentSLC2A11.83
24StrabismusEnrichmentSLC2A11.80
25EpilepsyEnrichmentSLC2A11.63
26Benign epilepsy with centrotemporal spikesEnrichmentSLC2A11.62
27Centralopathic epilepsyEnrichmentSLC2A11.60
28West syndromeEnrichmentSLC2A11.59
29Autism spectrum disorderEnrichmentHK11.20
30MicrocephalyEnrichmentSLC2A11.15
31Retinitis pigmentosaEnrichmentHK10.93
32Hereditary retinal dystrophyEnrichmentHK10.80
33Fundus dystrophyEnrichmentHK10.80

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