RUNX1 regulates transcription of genes involved in differentiation of myeloid cells

No Pathway Network information available for RUNX1 regulates transcription of genes involved in differentiation of myeloid cells

Pathways in the RUNX1 regulates transcription of genes involved in differentiation of myeloid cells SuperPath

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

Disorders associated with RUNX1 regulates transcription of genes involved in differentiation of myeloid cells SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Menke-hennekam syndrome 1EnrichmentCREBBP3.29
2Rubinstein-taybi syndrome due to 16p13.3 microdeletionEnrichmentCREBBP3.29
3Menke-hennekam syndromeEnrichmentCREBBP3.29
4Metaphyseal dysplasia with maxillary hypoplasia with or without brachydactylyEnrichmentRUNX23.23
5Storage pool platelet diseaseEnrichmentRUNX13.23
6Cleidocranial dysplasia 2EnrichmentCBFB3.23
7Tafro syndromeEnrichmentRUNX13.23
8Cleidocranial dysplasia 1EnrichmentRUNX23.05
9Platelet disorder, familial, with associated myeloid malignancyEnrichmentRUNX13.05
10Cleidocranial dysplasiaEnrichmentRUNX23.05
11Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with runx1EnrichmentRUNX13.05
12Thumb deformityEnrichmentCREBBP2.99
13Acute myeloid leukemia with kat6a-crebbp fusionEnrichmentCREBBP2.99
14Blood platelet diseaseEnrichmentRUNX12.93
15Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)EnrichmentCBFB2.93
16Aggressive systemic mastocytosisEnrichmentRUNX12.83
17Acute myeloid leukemia with t(8;21)(q22;q22) translocationEnrichmentRUNX12.83
18Tethered spinal cord syndromeEnrichmentCREBBP2.81
19Intraocular pressure quantitative trait locusEnrichmentCREBBP2.81
20PancytopeniaEnrichmentRUNX12.75
21Leukemia, chronic myeloidEnrichmentRUNX12.69
22Atypical chronic myeloid leukemia, bcr-abl1 negativeEnrichmentRUNX12.58
23Rubinstein-taybi syndrome 1EnrichmentCREBBP2.51
24Chromosome 16p13.3 deletion syndrome, proximalEnrichmentCREBBP2.51
25HypertrichosisEnrichmentCREBBP2.51
26Heart diseaseEnrichmentCREBBP2.14
27Corpus callosum, agenesis ofEnrichmentCREBBP2.11
28Isolated corpus callosum agenesisEnrichmentCREBBP2.11
29Rare genetic intellectual disabilityEnrichmentCREBBP2.11
30Intellectual disability-hypoplastic corpus callosum-preauricular tag syndromeEnrichmentCREBBP2.11
31Diffuse large b-cell lymphomaEnrichmentCREBBP2.01
32Leukemia, acute myeloidEnrichmentRUNX11.93
33ScoliosisEnrichmentCREBBP1.91
34Nephrotic syndromeEnrichmentRUNX21.90
35ThrombocytopeniaEnrichmentRUNX11.85
36Myeloma, multipleEnrichmentCREBBP1.54
37AutismEnrichmentCREBBP1.44
38Inherited cancer-predisposing syndromeEnrichmentRUNX11.42
39Congenital nervous system abnormalityEnrichmentCREBBP1.27
40Nervous system diseaseEnrichmentCREBBP1.27

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