Glycerophospholipid biosynthetic pathway

Pathway network for the Glycerophospholipid biosynthetic pathway SuperPath

Sources:
  • WikiPathways
  • PubChem
  • Reactome

Gene overlap in member pathways for Glycerophospholipid biosynthetic pathway SuperPath

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

Disorders associated with Glycerophospholipid biosynthetic pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Rhizomelic chondrodysplasia punctataEnrichmentAGPS, GNPAT4.55
2Combined oxidative phosphorylation deficiency 57EnrichmentCRLS14.13
3Neurodevelopmental disorder with ataxia and brain abnormalitiesEnrichmentPTPMT13.66
4MacrodactylyEnrichmentPIK3CA2.66
5Lenz-majewski hyperostotic dwarfismEnrichmentPTDSS12.66
6Rhizomelic chondrodysplasia punctata, type 2EnrichmentGNPAT2.66
7Megalencephaly, autosomal dominantEnrichmentPIK3CA2.66
8Cowden syndrome 5EnrichmentPIK3CA2.66
9Hypertriglyceridemia, transient infantileEnrichmentGPD12.66
10Cerebral cavernous malformations 4EnrichmentPIK3CA2.66
11Rhizomelic chondrodysplasia punctata, type 3EnrichmentAGPS2.66
12Proximal myopathy with focal depletion of mitochondriaEnrichmentCHKB2.66
13Hemifacial myohyperplasiaEnrichmentPIK3CA2.66
14Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowthEnrichmentPIK3CA2.66
15Majeed syndromeEnrichmentLPIN22.66
16Immunodeficiency 14b, autosomal recessiveEnrichmentPIK3CD2.66
17Immunodeficiency 97 with autoinflammationEnrichmentPIK3CG2.66
18Hereditary neuroendocrine tumor of small intestineEnrichmentIPMK2.66
19Segmental progressive overgrowth syndrome with fibroadipose hyperplasiaEnrichmentPIK3CA2.66
20HypospadiasEnrichmentPIK3CA2.66
21Rare venous malformationEnrichmentPIK3CA2.66
22Diaphragmatic eventrationEnrichmentPIK3CA2.66
23Pik3ca-related overgrowth spectrumEnrichmentPIK3CA2.66
24Rare combined vascular malformationEnrichmentPIK3CA2.66
25Cavernous lymphangiomaEnrichmentPIK3CA2.66
26Pik3ca-related overgrowth syndromeEnrichmentPIK3CA2.66
27Hemihyperplasia-multiple lipomatosis syndromeEnrichmentPIK3CA2.66
28Eccrine angiomatous hamartomaEnrichmentPIK3CA2.66
29Macrodactyly of toeEnrichmentPIK3CA2.66
30Glycerol kinase deficiencyEnrichmentGK2.35
31Keratosis, seborrheicEnrichmentPIK3CA2.35
32Roifman-chitayat syndromeEnrichmentPIK3CD2.35
33Noonan syndrome 8EnrichmentPIK3CA2.35
34Spastic paraplegia 82, autosomal recessiveEnrichmentPCYT22.35
35Rosette-forming glioneuronal tumorEnrichmentPIK3CA2.35
36Intellectual developmental disorder, autosomal dominant 60, with seizuresEnrichmentPIP5K1A2.35
37Immune system diseaseEnrichmentPIK3CD2.35
38Neurodevelopmental disorder with hyperkinetic movements, seizures, and structural brain abnormalitiesEnrichmentPI4K2A2.35
39Transient infantile hypertriglyceridemia and hepatosteatosisEnrichmentGPD12.35
40Pompe disease, infantile-onsetEnrichmentPIK3CA2.18
41Myoglobinuria, acute recurrent, autosomal recessiveEnrichmentLPIN12.18
42Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3CA2.18
43Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3CD2.18
44Immunodeficiency 14EnrichmentPIK3CD2.18
45KeratoacanthomaEnrichmentPIK3CA2.18
46Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentPIK3CA2.05
47Muscular dystrophy, congenital, megaconial typeEnrichmentCHKB2.05
48Cerebrovascular diseaseEnrichmentPIK3CA2.05
49Hereditary recurrent myoglobinuriaEnrichmentLPIN12.05
50Familial cerebral cavernous malformationsEnrichmentPIK3CA2.05
51Capillary malformations, congenitalEnrichmentPIK3CA1.96
52HemimegalencephalyEnrichmentPIK3CA1.96
53Klippel-trenaunay-weber syndromeEnrichmentPIK3CA1.88
54Cowden syndrome 1EnrichmentPIK3CA1.88
55Hemihyperplasia, isolatedEnrichmentPIK3CA1.88
56Breast adenocarcinomaEnrichmentPIK3CA1.88
57Lung squamous cell carcinomaEnrichmentPIK3CA1.88
58Nevus, epidermalEnrichmentPIK3CA1.81
59Capillary malformation-arteriovenous malformation 1EnrichmentPIK3CA1.81
60Gallbladder cancerEnrichmentPIK3CA1.81
61Colorectal cancerEnrichmentPIK3CA, PLA2G2A1.80
62Arteriovenous malformationEnrichmentPIK3CA1.70
63Adult hepatocellular carcinomaEnrichmentPIK3CA1.70
64Cowden syndromeEnrichmentPIK3CA1.70
65Myopathy, x-linked, with excessive autophagyEnrichmentPIK3CA1.66
66Familial colorectal cancerEnrichmentPLA2G2A1.66
67Autosomal non-syndromic agammaglobulinemiaEnrichmentPIK3CD1.66
68Lung non-small cell carcinomaEnrichmentPIK3CA1.62
69MeningiomaEnrichmentPIK3CA1.58
70Lip and oral cavity carcinomaEnrichmentPIK3CA1.58
71Nk-cell enteropathyEnrichmentPIK3CB1.55
72Lynch syndromeEnrichmentPIK3CA1.49
73Endometrial cancerEnrichmentPIK3CA1.34
74Hepatocellular carcinomaEnrichmentPIK3CA1.32
75Autoinflammatory diseaseEnrichmentLPIN21.29
76Muscular dystrophyEnrichmentCHKB1.29
77Bladder cancerEnrichmentPIK3CA1.21
78Prostate cancerEnrichmentPIK3CA1.21
79Lung cancerEnrichmentPIK3CA1.16
80Male infertilityEnrichmentGPAT21.14
81Gastric cancerEnrichmentPIK3CA1.04
82Hereditary breast carcinomaEnrichmentPIK3CA1.03
83HypertelorismEnrichmentPIK3CA0.96
84Breast cancerEnrichmentPIK3CA0.81
85Ovarian cancerEnrichmentPIK3CA0.70

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