RUNX1 regulates transcription of genes involved in WNT signaling

No Pathway Network information available for RUNX1 regulates transcription of genes involved in WNT signaling

Pathways in the RUNX1 regulates transcription of genes involved in WNT signaling SuperPath

#	Name	Source	Genes
1	RUNX1 regulates transcription of genes involved in WNT signaling	Reactome	AXIN1 CBFB ESR1 FOXP3 RSPO3 RUNX1 (see all 6) (see less)

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

#	Symbol	Description	Category	# Related Pathways
1	ESR1	Estrogen Receptor 1	Protein Coding	1
2	FOXP3	Forkhead Box P3~Name Same As:- HGNC:13781	Protein Coding	1
3	AXIN1	Axin 1	Protein Coding	1
4	RSPO3	R-Spondin 3	Protein Coding	1
5	RUNX1	RUNX Family Transcription Factor 1	Protein Coding	1
6	CBFB	Core-Binding Factor Subunit Beta	Protein Coding	1

Disorders associated with RUNX1 regulates transcription of genes involved in WNT signaling SuperPath

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Immunodysregulation, polyendocrinopathy, and enteropathy, x-linked	Enrichment	FOXP3	3.35
2	Caudal duplication anomaly	Enrichment	AXIN1	3.35
3	Craniometadiaphyseal osteosclerosis with hip dysplasia	Enrichment	AXIN1	3.35
4	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly	Enrichment	FOXP3	3.05
5	Storage pool platelet disease	Enrichment	RUNX1	3.05
6	Cleidocranial dysplasia 2	Enrichment	CBFB	3.05
7	Tafro syndrome	Enrichment	RUNX1	3.05
8	Platelet disorder, familial, with associated myeloid malignancy	Enrichment	RUNX1	2.88
9	Estrogen resistance	Enrichment	ESR1	2.88
10	Migraine without aura	Enrichment	ESR1	2.88
11	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with runx1	Enrichment	RUNX1	2.88
12	Arthrogryposis multiplex congenita 3, myogenic type	Enrichment	ESR1	2.75
13	Blood platelet disease	Enrichment	RUNX1	2.75
14	Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)	Enrichment	CBFB	2.75
15	Aggressive systemic mastocytosis	Enrichment	RUNX1	2.66
16	Acute myeloid leukemia with t(8;21)(q22;q22) translocation	Enrichment	RUNX1	2.66
17	Type 1 diabetes mellitus	Enrichment	FOXP3	2.58
18	Pancytopenia	Enrichment	RUNX1	2.58
19	Leukemia, chronic myeloid	Enrichment	RUNX1	2.51
20	Atypical chronic myeloid leukemia, bcr-abl1 negative	Enrichment	RUNX1	2.40
21	Adult hepatocellular carcinoma	Enrichment	AXIN1	2.40
22	Hydrops fetalis	Enrichment	FOXP3	2.40
23	Migraine with or without aura 1	Enrichment	ESR1	2.31
24	Centronuclear myopathy	Enrichment	FOXP3	2.03
25	Hepatocellular carcinoma	Enrichment	AXIN1	2.01
26	Myocardial infarction	Enrichment	ESR1	2.01
27	Leukemia, acute myeloid	Enrichment	RUNX1	1.76
28	Hereditary breast carcinoma	Enrichment	ESR1	1.71
29	Thrombocytopenia	Enrichment	RUNX1	1.68
30	Breast cancer	Enrichment	ESR1	1.49
31	Inherited cancer-predisposing syndrome	Enrichment	RUNX1	1.24

¹ WikiPathways

² PubChem

³ R&D Systems

⁴ Reactome

⁵ GeneGo (Thomson Reuters)

⁶ QIAGEN

⁷ PharmGKB

⁸ Cell Signaling Technology

⁹ Sino Biological

¹⁰ Tocris

¹¹ MalaCards

RUNX1 regulates transcription of genes involved in WNT signaling

Pathway Network for RUNX1 regulates transcription of genes involved in WNT signaling

Member Pathways for RUNX1 regulates transcription of genes involved in WNT signaling

Pathways in the RUNX1 regulates transcription of genes involved in WNT signaling SuperPath

Associated Genes for RUNX1 regulates transcription of genes involved in WNT signaling

Associated Disorders for RUNX1 regulates transcription of genes involved in WNT signaling

Disorders associated with RUNX1 regulates transcription of genes involved in WNT signaling SuperPath

STRING Interaction Network for RUNX1 regulates transcription of genes involved in WNT signaling

Sources for RUNX1 regulates transcription of genes involved in WNT signaling