Signaling mediated by p38-gamma and p38-delta

No Pathway Network information available for Signaling mediated by p38-gamma and p38-delta

#	Name	Source	Genes
1	Signaling mediated by p38-gamma and p38-delta	PubChem	CCND1 EEF2K MAP2K3 MAP2K6 MAP3K20 MAPK12 MAPK13 MAPT PKN1 SNTA1 STMN1 (see all 11) (see less)

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

#	Symbol	Description	Category	# Related Pathways
1	MAP3K20	Mitogen-Activated Protein Kinase Kinase Kinase 20	Protein Coding	1
2	MAPK13	Mitogen-Activated Protein Kinase 13	Protein Coding	1
3	MAP2K3	Mitogen-Activated Protein Kinase Kinase 3	Protein Coding	1
4	SNTA1	Syntrophin Alpha 1	Protein Coding	1
5	EEF2K	Eukaryotic Elongation Factor 2 Kinase	Protein Coding	1
6	PKN1	Protein Kinase N1	Protein Coding	1
7	MAPK12	Mitogen-Activated Protein Kinase 12	Protein Coding	1
8	CCND1	Cyclin D1	Protein Coding	1
9	STMN1	Stathmin 1	Protein Coding	1
10	MAPT	Microtubule Associated Protein Tau	Protein Coding	1
11	MAP2K6	Mitogen-Activated Protein Kinase Kinase 6	Protein Coding	1

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Myopathy, centronuclear, 6, with fiber-type disproportion	Enrichment	MAP3K20	3.09
2	Parkinson-dementia syndrome	Enrichment	MAPT	3.09
3	Supranuclear palsy, progressive, 1	Enrichment	MAPT	3.09
4	Progressive supranuclear palsy	Enrichment	MAPT	3.09
5	Long qt syndrome 12	Enrichment	SNTA1	3.09
6	Classic progressive supranuclear palsy syndrome	Enrichment	MAPT	3.09
7	Atypical progressive supranuclear palsy syndrome	Enrichment	MAPT	3.09
8	Pick disease of brain	Enrichment	MAPT	2.79
9	Split-foot malformation with mesoaxial polydactyly	Enrichment	MAP3K20	2.79
10	Mantle cell lymphoma	Enrichment	CCND1	2.49
11	Atrial fibrillation	Enrichment	SNTA1	2.49
12	Von hippel-lindau syndrome	Enrichment	CCND1	2.39
13	Dementia	Enrichment	MAPT	2.39
14	Split-hand/foot malformation 1	Enrichment	MAP3K20	2.31
15	Semantic dementia	Enrichment	MAPT	2.25
16	Progressive non-fluent aphasia	Enrichment	MAPT	2.14
17	Behavioral variant of frontotemporal dementia	Enrichment	MAPT	2.14
18	Leukemia, chronic lymphocytic	Enrichment	CCND1	2.09
19	Frontotemporal dementia 1	Enrichment	MAPT	2.05
20	Alzheimer's disease	Enrichment	MAPT	1.98
21	Congenital myopathy 4a, autosomal dominant	Enrichment	MAP3K20	1.92
22	Alzheimer disease, familial, 1	Enrichment	MAPT	1.86
23	Centronuclear myopathy	Enrichment	MAP3K20	1.77
24	Parkinson disease, late-onset	Enrichment	MAPT	1.71
25	Long qt syndrome 1	Enrichment	SNTA1	1.62
26	Long qt syndrome	Enrichment	SNTA1	1.60
27	Myeloma, multiple	Enrichment	CCND1	1.35
28	Frontotemporal dementia and/or amyotrophic lateral sclerosis 7	Enrichment	MAPT	1.34
29	Colorectal cancer	Enrichment	CCND1	1.17

¹ WikiPathways

² PubChem

³ R&D Systems

⁴ Reactome

⁵ GeneGo (Thomson Reuters)

⁶ QIAGEN

⁷ PharmGKB

⁹ Sino Biological

¹⁰ Tocris

¹¹ MalaCards

Pathway Network for Signaling mediated by p38-gamma and p38-delta