Protein methylation

No Pathway Network information available for Protein methylation

Pathways in the Protein methylation SuperPath

#	Name	Source	Genes
1	Protein methylation	Reactome	CALM1 CALM2 CALM3 CAMKMT EEF1A1 EEF1AKMT1 EEF1AKMT2 EEF2 EEF2KMT ETFB ETFBKMT HSPA8 KIN METTL21A METTL22 PRMT3 RPS2 VCP VCPKMT (see all 19) (see less)

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

#	Symbol	Description	Category	# Related Pathways
1	PRMT3	Protein Arginine Methyltransferase 3	Protein Coding	1
2	METTL21A	Methyltransferase 21A, HSPA Lysine	Protein Coding	1
3	EEF1A1	Eukaryotic Translation Elongation Factor 1 Alpha 1	Protein Coding	1
4	EEF2	Eukaryotic Translation Elongation Factor 2	Protein Coding	1
5	EEF2KMT	Eukaryotic Elongation Factor 2 Lysine Methyltransferase	Protein Coding	1
6	ETFB	Electron Transfer Flavoprotein Subunit Beta	Protein Coding	1
7	EEF1AKMT1	EEF1A Lysine Methyltransferase 1	Protein Coding	1
8	KIN	Kin17 DNA And RNA Binding Protein	Protein Coding	1
9	ETFBKMT	Electron Transfer Flavoprotein Subunit Beta Lysine Methyltransferase	Protein Coding	1
10	HSPA8	Heat Shock Protein Family A (Hsp70) Member 8	Protein Coding	1
11	EEF1AKMT2	EEF1A Lysine Methyltransferase 2	Protein Coding	1
12	RPS2	Ribosomal Protein S2	Protein Coding	1
13	VCP	Valosin Containing Protein	Protein Coding	1
14	METTL22	Methyltransferase 22, Kin17 Lysine	Protein Coding	1
15	VCPKMT	Valosin Containing Protein Lysine Methyltransferase	Protein Coding	1
16	CAMKMT	Calmodulin-Lysine N-Methyltransferase	Protein Coding	1
17	CALM1	Calmodulin 1	Protein Coding	1
18	CALM2	Calmodulin 2	Protein Coding	1
19	CALM3	Calmodulin 3	Protein Coding	1

Disorders associated with Protein methylation SuperPath

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Catecholaminergic polymorphic ventricular tachycardia	Enrichment	CALM1, CALM2, CALM3	6.89
2	Long qt syndrome 1	Enrichment	CALM1, CALM2, CALM3	5.03
3	Long qt syndrome	Enrichment	CALM1, CALM2	3.07
4	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1	Enrichment	VCP	2.85
5	Spinocerebellar ataxia 26	Enrichment	EEF2	2.85
6	Long qt syndrome 16	Enrichment	CALM3	2.85
7	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6	Enrichment	VCP	2.85
8	Multisystem proteinopathy	Enrichment	VCP	2.85
9	Long qt syndrome 15	Enrichment	CALM2	2.85
10	Adult-onset distal myopathy due to vcp mutation	Enrichment	VCP	2.85
11	Amyotrophic lateral sclerosis 6 with or without frontotemporal dementia	Enrichment	VCP	2.55
12	Ventricular tachycardia, catecholaminergic polymorphic, 4	Enrichment	CALM1	2.55
13	Long qt syndrome 14	Enrichment	CALM1	2.55
14	2p21 microdeletion syndrome without cystinuria	Enrichment	CAMKMT	2.55
15	Spastic paraplegia-paget disease of bone syndrome	Enrichment	VCP	2.55
16	Inclusion body myopathy with paget disease of bone and frontotemporal dementia	Enrichment	VCP	2.38
17	Atypical hypotonia-cystinuria syndrome	Enrichment	CAMKMT	2.38
18	Multiple acyl-coa dehydrogenase deficiency	Enrichment	ETFB	2.25
19	Congenital disorder of glycosylation, type ik	Enrichment	EEF2KMT	2.25
20	2p21 microdeletion syndrome	Enrichment	CAMKMT	2.25
21	Dementia, lewy body	Enrichment	VCP	2.16
22	Charcot-marie-tooth disease, axonal, type 2e	Enrichment	VCP	2.16
23	Multiple acyl-coa dehydrogenase deficiency, severe neonatal type	Enrichment	ETFB	2.16
24	Multiple acyl-coa dehydrogenase deficiency, mild type	Enrichment	ETFB	2.16
25	Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy	Enrichment	CALM1	2.08
26	Catecholaminergic polymorphic ventricular tachycardia 1	Enrichment	CALM1	1.95
27	Progressive non-fluent aphasia	Enrichment	VCP	1.90
28	Behavioral variant of frontotemporal dementia	Enrichment	VCP	1.90
29	Frontotemporal dementia and/or amyotrophic lateral sclerosis 1	Enrichment	VCP	1.86
30	Alzheimer's disease	Enrichment	VCP	1.74
31	Alzheimer disease, familial, 1	Enrichment	VCP	1.63
32	Sudden infant death syndrome	Enrichment	CALM2	1.63
33	Congenital disorder of glycosylation, type in	Enrichment	EEF2KMT	1.63
34	Neuropathy, hereditary motor and sensory, okinawa type	Enrichment	VCP	1.58
35	Frontotemporal dementia and/or amyotrophic lateral sclerosis 7	Enrichment	VCP	1.11

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

Protein methylation

Pathway Network for Protein methylation

Member Pathways for Protein methylation

Pathways in the Protein methylation SuperPath

Associated Genes for Protein methylation

Associated Disorders for Protein methylation

Disorders associated with Protein methylation SuperPath

STRING Interaction Network for Protein methylation

Sources for Protein methylation