Insertion of tail-anchored proteins into the endoplasmic reticulum membrane

No Pathway Network information available for Insertion of tail-anchored proteins into the endoplasmic reticulum membrane

Pathways in the Insertion of tail-anchored proteins into the endoplasmic reticulum membrane SuperPath

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

Disorders associated with Insertion of tail-anchored proteins into the endoplasmic reticulum membrane SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Cystic fibrosisEnrichmentHMOX1, STX1A2.92
2Fatal familial insomniaEnrichmentPRNP2.79
3Gerstmann-straussler diseaseEnrichmentPRNP2.79
4KuruEnrichmentPRNP2.79
5Cardiomyopathy, dilated, 2hEnrichmentGET32.79
6Congenital disorder of glycosylation, type iizEnrichmentCAMLG2.79
7Spongiform encephalopathy with neuropsychiatric featuresEnrichmentPRNP2.79
8Huntington disease-like 1EnrichmentPRNP2.79
9Arthrogryposis and ectodermal dysplasiaEnrichmentOTOF2.79
10Cerebral amyloid angiopathy, app-relatedEnrichmentAPP2.79
11Congenital disorder of glycosylation, type iiaaEnrichmentSTX52.79
12Familial alzheimer-like prion diseaseEnrichmentPRNP2.79
13Neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movementsEnrichmentVAMP22.79
14Heme oxygenase 1 deficiencyEnrichmentHMOX12.79
15Prion diseaseEnrichmentPRNP2.79
16Congenital disorder of glycosylation, type iiyEnrichmentGET42.79
17Prp systemic amyloidosisEnrichmentPRNP2.79
18Inherited human prion diseaseEnrichmentPRNP2.79
19Inherited creutzfeldt-jakob diseaseEnrichmentPRNP2.79
20Cerebral amyloid angiopathy, cst3-relatedEnrichmentAPP2.49
21Methemoglobinemia and ambiguous genitaliaEnrichmentCYB5A2.49
22Myopathy, x-linked, with postural muscle atrophyEnrichmentEMD2.49
23Creutzfeldt-jakob diseaseEnrichmentPRNP2.49
24Sjogren-larsson syndromeEnrichmentALDH3A22.49
25Hereditary methemoglobinemiaEnrichmentCYB5A2.49
26X-linked emery-dreifuss muscular dystrophyEnrichmentEMD2.49
27Adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiencyEnrichmentCYB5A2.31
28Deafness, autosomal recessive 3EnrichmentOTOF2.31
29Emery-dreifuss muscular dystrophy 1, x-linkedEnrichmentEMD2.19
30Frontotemporal dementia 2EnrichmentPRNP2.19
31Emery-dreifuss muscular dystrophyEnrichmentEMD2.19
32Deafness, autosomal recessive 9EnrichmentOTOF2.09
33Otof-related hearing lossEnrichmentOTOF2.09
34Alzheimer's disease 1EnrichmentAPP1.95
35Early-onset autosomal dominant alzheimer diseaseEnrichmentAPP1.95
36Pulmonary disease, chronic obstructiveEnrichmentHMOX11.68
37Alzheimer's diseaseEnrichmentAPP1.68
38Alzheimer disease, familial, 1EnrichmentAPP1.56
39Neuromuscular diseaseEnrichmentEMD1.54
40Neuropathy, hereditary motor and sensory, okinawa typeEnrichmentEMD1.52
41Williams-beuren syndromeEnrichmentSTX1A1.50
42Ear malformationEnrichmentOTOF1.42
43Auditory neuropathyEnrichmentOTOF1.38
44Non-syndromic genetic deafnessEnrichmentOTOF1.25
45Cerebral palsyEnrichmentALDH3A21.21
46MyopathyEnrichmentEMD1.20
47Nonsyndromic hearing lossEnrichmentOTOF1.18
48Familial isolated dilated cardiomyopathyEnrichmentGET31.08
49Deafness, autosomal recessiveEnrichmentOTOF1.01
50Autosomal recessive nonsyndromic deafnessEnrichmentOTOF1.00
51AutismEnrichmentSTX1A0.96
52Rare genetic deafnessEnrichmentOTOF0.92
53Dilated cardiomyopathyEnrichmentEMD0.91
54Rare autosomal recessive non-syndromic sensorineural deafness type dfnbEnrichmentOTOF0.87

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