Basigin interactions

No Pathway Network information available for Basigin interactions

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

Disorders associated with Basigin interactions SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Hydrocephalus due to congenital stenosis of aqueduct of sylviusEnrichmentL1CAM2.73
2Lipodystrophy, congenital generalized, type 3EnrichmentCAV12.73
3Erythrocyte lactate transporter defectEnrichmentSLC16A12.73
4Pulmonary hypertension, primary, 3EnrichmentCAV12.73
5Corpus callosum, partial agenesis of, x-linkedEnrichmentL1CAM2.73
6Hydrocephalus, congenital, x-linkedEnrichmentL1CAM2.73
7Masa syndromeEnrichmentL1CAM2.73
8Lipodystrophy, familial partial, type 7EnrichmentCAV12.73
9Spastic paraplegia 75, autosomal recessiveEnrichmentMAG2.73
10X-linked complicated spastic paraplegia type 1EnrichmentL1CAM2.73
11Monocarboxylate transporter 1 deficiencyEnrichmentSLC16A12.43
12Epidermolysis bullosa, junctional 7, with interstitial lung disease and nephrotic syndromeEnrichmentITGA32.43
13Recessive dystrophic epidermolysis bullosaEnrichmentMMP12.43
14Hyperinsulinemic hypoglycemia, familial, 7EnrichmentSLC16A12.43
15Ketoacidosis due to monocarboxylate transporter-1 deficiencyEnrichmentSLC16A12.43
16Lysinuric protein intoleranceEnrichmentSLC7A72.26
17Epidermolysis bullosa, junctional 6, with pyloric atresiaEnrichmentITGA62.26
18CystinuriaEnrichmentSLC7A92.13
19Muscular dystrophy, limb-girdle, autosomal recessive 23EnrichmentL1CAM2.04
20Epidermolysis bullosaEnrichmentITGA62.04
21Diffuse cutaneous systemic sclerosisEnrichmentCAV12.04
22Epidermolysis bullosa, junctional 5b, with pyloric atresiaEnrichmentITGA61.96
23Limited sclerodermaEnrichmentCAV11.96
24Junctional epidermolysis bullosaEnrichmentITGA61.78
25Hydrops fetalisEnrichmentL1CAM1.78
26Heritable pulmonary arterial hypertensionEnrichmentCAV11.70
27Neural tube defectsEnrichmentITGB11.63
28CataractEnrichmentSLC7A81.59
29Hypertension, essentialEnrichmentATP1B11.51
30Autoinflammatory diseaseEnrichmentSLC7A71.36
31Nephrotic syndromeEnrichmentITGA31.12

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