Telomere Extension by Telomerase

No Pathway Network information available for Telomere Extension by Telomerase

Pathways in the Telomere Extension by Telomerase SuperPath

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

Disorders associated with Telomere Extension by Telomerase SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Melanoma, cutaneous malignant 1EnrichmentPOT1, TERF2IP, TERT5.81
2Dyskeratosis congenitaEnrichmentPOT1, TERT, TINF25.65
3Hepatocellular carcinomaEnrichmentNBN, RAD50, TERT5.45
4Inclusion body myopathy with paget disease of bone and frontotemporal dementiaEnrichmentHNRNPA1, HNRNPA2B15.25
5Nijmegen breakage syndrome-like disorderEnrichmentMRE11, RAD504.95
6Dyskeratosis congenita, autosomal dominant 1EnrichmentTERT, TINF24.56
7Hoyeraal-hreidarsson syndromeEnrichmentTERT, TINF24.56
8Inherited cancer-predisposing syndromeEnrichmentMRE11, NBN, POT1, RAD504.53
9Dyskeratosis congenita, autosomal dominant 2EnrichmentTERT, TINF24.41
10Hereditary breast ovarian cancer syndromeEnrichmentMRE11, NBN, RAD504.23
11Aplastic anemiaEnrichmentNBN, TERT4.08
12Breast cancerEnrichmentMRE11, NBN, RAD503.83
13Ovarian cancerEnrichmentMRE11, NBN, RAD503.45
14Tumor predisposition syndrome 3EnrichmentPOT12.85
15Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3EnrichmentHNRNPA12.85
16Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8EnrichmentPOT12.85
17Ataxia-telangiectasia-like disorder 1EnrichmentMRE112.85
18Myopathy, distal, 3EnrichmentHNRNPA12.85
19High-grade astrocytoma with piloid featuresEnrichmentPOT12.85
20Cerebroretinal microangiopathy with calcifications and cysts 3EnrichmentPOT12.85
21Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2EnrichmentHNRNPA2B12.85
22Amyotrophic lateral sclerosis 20EnrichmentHNRNPA12.85
23Finnish upper limb-onset distal myopathyEnrichmentHNRNPA12.85
24Autosomal recessive dyskeratosis congenita 4EnrichmentTERT2.85
25Intellectual developmental disorder, autosomal dominant 74EnrichmentHNRNPC2.85
26Oculopharyngeal muscular dystrophy 2EnrichmentHNRNPA2B12.85
27Relapsing-remitting multiple sclerosisEnrichmentHNRNPA12.85
28Hereditary breast carcinomaEnrichmentNBN, RAD502.77
29Revesz syndromeEnrichmentTINF22.55
30Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 1EnrichmentTERT2.55
31Dyskeratosis congenita, autosomal dominant 3EnrichmentTINF22.55
32OligodendrogliomaEnrichmentPOT12.55
33Melanoma, cutaneous malignant 9EnrichmentTERT2.55
34Idiopathic interstitial pneumoniaEnrichmentTERT2.55
35Anaplastic oligodendrogliomaEnrichmentPOT12.55
36Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentHNRNPA1, HNRNPA2B12.53
37Nijmegen breakage syndromeEnrichmentNBN2.38
38Distal myopathyEnrichmentHNRNPA12.38
39Interstitial lung diseaseEnrichmentTERT2.38
40Macrocytic anemiaEnrichmentTERT2.38
41Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemiaEnrichmentMRE112.25
42Myopathy, autophagic vacuolar, infantile-onsetEnrichmentHNRNPA2B12.25
43Lung sarcomatoid carcinomaEnrichmentTERT2.25
44Idiopathic aplastic anemiaEnrichmentTERT2.16
45Pulmonary fibrosisEnrichmentTERT2.08
46Adrenocortical carcinomaEnrichmentTERT2.08
47Kidney clear cell sarcomaEnrichmentTERT2.08
48Colonic benign neoplasmEnrichmentMRE111.90
49Leukemia, chronic lymphocyticEnrichmentPOT11.86
50Leukemia, acute lymphoblasticEnrichmentNBN1.82
51MeningiomaEnrichmentTERT1.78
52Breast-ovarian cancer, familial 1EnrichmentNBN1.74
53Premature menopauseEnrichmentNBN1.74
54Interstitial lung disease 2EnrichmentTERT1.63
55Diffuse large b-cell lymphomaEnrichmentNBN1.58
56LissencephalyEnrichmentNBN1.54
57HepatoblastomaEnrichmentTERT1.54
58Pancreatic cancerEnrichmentNBN1.46
59Bladder cancerEnrichmentTERT1.40
60Prostate cancerEnrichmentNBN1.40
61Differentiated thyroid carcinomaEnrichmentTERT1.40
62Leukemia, acute myeloidEnrichmentTERT1.26
63Gastric cancerEnrichmentNBN1.23
64Primary ovarian insufficiencyEnrichmentNBN1.10
65MicrocephalyEnrichmentNBN0.80
66Complex neurodevelopmental disorderEnrichmentHNRNPC0.80

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