PERK regulates gene expression

No Pathway Network information available for PERK regulates gene expression

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

Disorders associated with PERK regulates gene expression SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Pontocerebellar hypoplasia, type 1eEnrichmentEXOSC3, EXOSC8, EXOSC96.85
2Pontocerebellar hypoplasiaEnrichmentEXOSC3, EXOSC93.24
3Dyskeratosis congenita, autosomal recessive 6EnrichmentPARN2.70
4Pontocerebellar hypoplasia, type 1fEnrichmentEXOSC12.70
5Cerebellar ataxia, brain abnormalities, and cardiac conduction defectsEnrichmentEXOSC52.70
6Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 4EnrichmentPARN2.70
7Achromatopsia 7EnrichmentATF62.70
8Pontocerebellar hypoplasia, type 1cEnrichmentEXOSC82.70
9Pontocerebellar hypoplasia, type 1dEnrichmentEXOSC92.70
10Short stature, hearing loss, retinitis pigmentosa, and distinctive faciesEnrichmentEXOSC22.70
11Mehmo syndromeEnrichmentEIF2S32.63
12Congenital pontocerebellar hypoplasia type 1EnrichmentEXOSC32.40
13Epiphyseal dysplasia, multiple, with early-onset diabetes mellitusEnrichmentEIF2AK32.33
14Pontocerebellar hypoplasia, type 1bEnrichmentEXOSC32.22
15Cerebellar diseaseEnrichmentEXOSC32.22
16Asparagine synthetase deficiencyEnrichmentASNS2.22
17Myxoid liposarcomaEnrichmentDDIT32.22
18Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndromeEnrichmentASNS2.22
19Spinocerebellar ataxia, autosomal recessive 29EnrichmentASNS2.22
20Menkes diseaseEnrichmentEIF2AK32.15
21Pulmonary fibrosisEnrichmentPARN1.92
22Hoyeraal-hreidarsson syndromeEnrichmentPARN1.92
23AchromatopsiaEnrichmentATF61.70
24Interstitial lung disease 2EnrichmentPARN1.48
25Human immunodeficiency virus type 1EnrichmentCCL21.45
26Congenital myopathyEnrichmentEXOSC31.43
27Dyskeratosis congenitaEnrichmentPARN1.43
28LissencephalyEnrichmentEXOSC31.39
29Fetal akinesia deformation sequence 1EnrichmentEXOSC31.15
30Spastic ataxiaEnrichmentEXOSC81.00
31Hereditary breast ovarian cancer syndromeEnrichmentHERPUD10.98
32Myeloma, multipleEnrichmentDIS30.98
33Cone-rod dystrophy 2EnrichmentATF60.90
34Congenital nervous system abnormalityEnrichmentEXOSC30.72
35Nervous system diseaseEnrichmentEXOSC30.72
36MicrocephalyEnrichmentEXOSC30.66
37Hereditary retinal dystrophyEnrichmentATF60.35
38Fundus dystrophyEnrichmentATF60.35

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