Lactate shuttle in glial cells

No Pathway Network information available for Lactate shuttle in glial cells

Pathways in the Lactate shuttle in glial cells SuperPath

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

Disorders associated with Lactate shuttle in glial cells SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Anemia, congenital, nonspherocytic hemolytic, 5EnrichmentHK13.05
2Retinitis pigmentosa 17EnrichmentCA43.05
3Stomatin-deficient cryohydrocytosis with neurologic defectsEnrichmentSLC2A13.05
4Erythrocyte lactate transporter defectEnrichmentSLC16A13.05
5Developmental and epileptic encephalopathy 41EnrichmentSLC1A23.05
6Retinitis pigmentosa 79EnrichmentHK13.05
7Neuropathy, hereditary motor and sensory, russe typeEnrichmentHK13.05
8Neurodevelopmental disorder with visual defects and brain anomaliesEnrichmentHK13.05
9Epilepsy, idiopathic generalized 12EnrichmentSLC2A13.05
10Epilepsy with myoclonic absencesEnrichmentSLC2A13.05
11Hereditary cryohydrocytosis with reduced stomatinEnrichmentSLC2A13.05
12Fanconi-bickel syndromeEnrichmentLDHA2.75
13Dystonia 9EnrichmentSLC2A12.75
14Glut1 deficiency syndrome 1EnrichmentSLC2A12.75
15Proximal renal tubular acidosis-ocular anomaly syndromeEnrichmentSLC4A42.75
16Monocarboxylate transporter 1 deficiencyEnrichmentSLC16A12.75
17Osteopetrosis, autosomal recessive 3EnrichmentCA22.75
18Glucose transporter type 1 deficiency syndromeEnrichmentSLC2A12.75
19Hyperinsulinemic hypoglycemia, familial, 7EnrichmentSLC16A12.75
20Autosomal recessive proximal renal tubular acidosisEnrichmentSLC4A42.75
21Ketoacidosis due to monocarboxylate transporter-1 deficiencyEnrichmentSLC16A12.75
22Glut1 deficiency syndrome 2EnrichmentSLC2A12.58
23Chromosome 17q23.1-q23.2 deletion syndromeEnrichmentSLC2A12.58
24Huntington diseaseEnrichmentSLC2A32.45
25OsteopetrosisEnrichmentCA22.35
26Paroxysmal dystoniaEnrichmentSLC2A12.21
27Alternating hemiplegia of childhoodEnrichmentSLC2A12.15
28Myoclonic-atonic epilepsyEnrichmentSLC2A12.10
29Retinitis pigmentosaEnrichmentCA4, HK11.84
30Developmental and epileptic encephalopathy 1EnrichmentSLC2A11.66
31StrabismusEnrichmentSLC2A11.63
32Hereditary retinal dystrophyEnrichmentCA4, HK11.58
33Fundus dystrophyEnrichmentCA4, HK11.58
34EpilepsyEnrichmentSLC2A11.46
35Benign epilepsy with centrotemporal spikesEnrichmentSLC2A11.45
36Centralopathic epilepsyEnrichmentSLC2A11.43
37West syndromeEnrichmentSLC2A11.42
38Undetermined early-onset epileptic encephalopathyEnrichmentSLC1A21.31
39Autism spectrum disorderEnrichmentHK11.03
40MicrocephalyEnrichmentSLC2A10.98

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