Synthesis of substrates in N-glycan biosythesis

Pathway network for the Synthesis of substrates in N-glycan biosythesis SuperPath

Sources:

Reactome

Pathways in the Synthesis of substrates in N-glycan biosythesis SuperPath

#	Name	Source	Genes
1	Synthesis of substrates in N-glycan biosythesis	Reactome	ALG5 AMDHD2 CMAS CTSA DHDDS DHRSX DOLK DOLPP1 DPM1 DPM2 DPM3 FCSK FPGT FUOM GFPT1 GFPT2 GFUS GLB1 GMDS GMPPA GMPPB GNE GNPNAT1 HK1 MPI MVD NAGK NANP NANS NEU1 NEU2 NEU3 NEU4 NPL NUDT14 NUS1 PGM3 PMM1 PMM2 RENBP SLC17A5 SLC35A1 SLC35C1 SRD5A3 ST3GAL1 ST3GAL2 ST3GAL3 ST3GAL4 ST3GAL5 ST3GAL6 ST6GAL1 ST6GAL2 ST6GALNAC1 ST6GALNAC2 ST6GALNAC3 ST6GALNAC4 ST6GALNAC5 ST6GALNAC6 ST8SIA1 ST8SIA2 ST8SIA3 ST8SIA4 ST8SIA5 ST8SIA6 UAP1 (see all 65) (see less)
2	Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein	Reactome	ALG1 ALG10 ALG10B ALG11 ALG12 ALG13 ALG14 ALG2 ALG3 ALG5 ALG6 ALG8 ALG9 AMDHD2 CMAS CTSA DHDDS DHRSX DOLK DOLPP1 DPAGT1 DPM1 DPM2 DPM3 FCSK FPGT FUOM GFPT1 GFPT2 GFUS GLB1 GMDS GMPPA GMPPB GNE GNPNAT1 HK1 MPDU1 MPI MVD NAGK NANP NANS NEU1 NEU2 NEU3 NEU4 NPL NUDT14 NUS1 PGM3 PMM1 PMM2 RENBP RFT1 SLC17A5 SLC35A1 SLC35C1 SRD5A3 ST3GAL1 ST3GAL2 ST3GAL3 ST3GAL4 ST3GAL5 ST3GAL6 ST6GAL1 ST6GAL2 ST6GALNAC1 ST6GALNAC2 ST6GALNAC3 ST6GALNAC4 ST6GALNAC5 ST6GALNAC6 ST8SIA1 ST8SIA2 ST8SIA3 ST8SIA4 ST8SIA5 ST8SIA6 UAP1 (see all 80) (see less)
3	Sialic acid metabolism	Reactome	CMAS CTSA GLB1 GNE NANP NANS NEU1 NEU2 NEU3 NEU4 NPL SLC17A5 SLC35A1 ST3GAL1 ST3GAL2 ST3GAL3 ST3GAL4 ST3GAL5 ST3GAL6 ST6GAL1 ST6GAL2 ST6GALNAC1 ST6GALNAC2 ST6GALNAC3 ST6GALNAC4 ST6GALNAC5 ST6GALNAC6 ST8SIA1 ST8SIA2 ST8SIA3 ST8SIA4 ST8SIA5 ST8SIA6 (see all 33) (see less)
4	Synthesis of UDP-N-acetyl-glucosamine	Reactome	AMDHD2 GFPT1 GFPT2 GNPNAT1 NAGK PGM3 RENBP UAP1 (see all 8) (see less)
5	Synthesis of dolichyl-phosphate	Reactome	DHDDS DHRSX DOLK DOLPP1 MVD NUS1 SRD5A3 (see all 7) (see less)
6	GDP-fucose biosynthesis	Reactome	FCSK FPGT FUOM GFUS GMDS SLC35C1 (see all 6) (see less)
7	Synthesis of GDP-mannose	Reactome	GMPPA GMPPB HK1 MPI PMM1 PMM2 (see all 6) (see less)
8	Defective DHDDS causes RP59	Reactome	DHDDS NUS1
9	Synthesis of dolichyl-phosphate-glucose	Reactome	ALG5 NUDT14
10	Defective PMM2 causes PMM2-CDG	Reactome	PMM2
11	Defective DOLK causes DOLK-CDG	Reactome	DOLK
12	Defective MPI causes MPI-CDG	Reactome	MPI
13	Defective SLC35C1 causes congenital disorder of glycosylation 2C (CDG2C)	Reactome	SLC35C1
14	Defective SRD5A3 causes SRD5A3-CDG, KHRZ	Reactome	SRD5A3

Gene overlap in member pathways for Synthesis of substrates in N-glycan biosythesis SuperPath

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

#	Symbol	Description	Category	# Related Pathways
1	NUS1	NUS1 Dehydrodolichyl Diphosphate Synthase Subunit	Protein Coding	4
2	DOLK	Dolichol Kinase	Protein Coding	4
3	MPI	Mannose Phosphate Isomerase	Protein Coding	4
4	PMM2	Phosphomannomutase 2	Protein Coding	4
5	SLC35C1	Solute Carrier Family 35 Member C1	Protein Coding	4
6	SRD5A3	Steroid 5 Alpha-Reductase 3	Protein Coding	4
7	DHDDS	Dehydrodolichyl Diphosphate Synthase Subunit	Protein Coding	4
8	GNE	Glucosamine (UDP-N-Acetyl)-2-Epimerase/N-Acetylmannosamine Kinase	Protein Coding	3
9	ST3GAL6	ST3 Beta-Galactoside Alpha-2,3-Sialyltransferase 6	Protein Coding	3
10	SLC35A1	Solute Carrier Family 35 Member A1	Protein Coding	3
11	ST6GALNAC2	ST6 N-Acetylgalactosaminide Alpha-2,6-Sialyltransferase 2	Protein Coding	3
12	NEU3	Neuraminidase 3	Protein Coding	3
13	NEU4	Neuraminidase 4	Protein Coding	3
14	NANP	N-Acetylneuraminic Acid Phosphatase	Protein Coding	3
15	FCSK	Fucose Kinase	Protein Coding	3
16	DHRSX	Dehydrogenase/Reductase X-Linked	Protein Coding	3
17	NUDT14	Nudix Hydrolase 14	Protein Coding	3
18	ST6GALNAC3	ST6 N-Acetylgalactosaminide Alpha-2,6-Sialyltransferase 3	Protein Coding	3
19	SLC17A5	Solute Carrier Family 17 Member 5	Protein Coding	3
20	GFPT1	Glutamine--Fructose-6-Phosphate Transaminase 1	Protein Coding	3
21	ST6GALNAC4	ST6 N-Acetylgalactosaminide Alpha-2,6-Sialyltransferase 4	Protein Coding	3
22	GLB1	Galactosidase Beta 1	Protein Coding	3
23	GMDS	GDP-Mannose 4,6-Dehydratase	Protein Coding	3
24	FUOM	Fucose Mutarotase	Protein Coding	3
25	ALG5	ALG5 Dolichyl-Phosphate Beta-Glucosyltransferase	Protein Coding	3
26	ST8SIA5	ST8 Alpha-N-Acetyl-Neuraminide Alpha-2,8-Sialyltransferase 5	Protein Coding	3
27	GMPPB	GDP-Mannose Pyrophosphorylase B	Protein Coding	3
28	GMPPA	GDP-Mannose Pyrophosphorylase A	Protein Coding	3
29	ST6GALNAC6	ST6 N-Acetylgalactosaminide Alpha-2,6-Sialyltransferase 6	Protein Coding	3
30	HK1	Hexokinase 1	Protein Coding	3
31	ST8SIA6	ST8 Alpha-N-Acetyl-Neuraminide Alpha-2,8-Sialyltransferase 6	Protein Coding	3
32	MVD	Mevalonate Diphosphate Decarboxylase	Protein Coding	3
33	NEU1	Neuraminidase 1	Protein Coding	3
34	NEU2	Neuraminidase 2	Protein Coding	3
35	AMDHD2	Amidohydrolase Domain Containing 2	Protein Coding	3
36	ST8SIA3	ST8 Alpha-N-Acetyl-Neuraminide Alpha-2,8-Sialyltransferase 3	Protein Coding	3
37	PGM3	Phosphoglucomutase 3	Protein Coding	3
38	PMM1	Phosphomannomutase 1	Protein Coding	3
39	NANS	N-Acetylneuraminate Synthase	Protein Coding	3
40	CTSA	Cathepsin A	Protein Coding	3
41	NAGK	N-Acetylglucosamine Kinase	Protein Coding	3
42	ST6GALNAC1	ST6 N-Acetylgalactosaminide Alpha-2,6-Sialyltransferase 1	Protein Coding	3
43	CMAS	Cytidine Monophosphate N-Acetylneuraminic Acid Synthetase	Protein Coding	3
44	DOLPP1	Dolichyldiphosphatase 1	Protein Coding	3
45	RENBP	Renin Binding Protein	Protein Coding	3
46	ST6GAL1	ST6 Beta-Galactoside Alpha-2,6-Sialyltransferase 1	Protein Coding	3
47	ST3GAL1	ST3 Beta-Galactoside Alpha-2,3-Sialyltransferase 1	Protein Coding	3
48	ST3GAL2	ST3 Beta-Galactoside Alpha-2,3-Sialyltransferase 2	Protein Coding	3
49	ST3GAL4	ST3 Beta-Galactoside Alpha-2,3-Sialyltransferase 4	Protein Coding	3
50	GNPNAT1	Glucosamine-Phosphate N-Acetyltransferase 1	Protein Coding	3
51	ST3GAL3	ST3 Beta-Galactoside Alpha-2,3-Sialyltransferase 3	Protein Coding	3
52	ST8SIA1	ST8 Alpha-N-Acetyl-Neuraminide Alpha-2,8-Sialyltransferase 1	Protein Coding	3
53	UAP1	UDP-N-Acetylglucosamine Pyrophosphorylase 1	Protein Coding	3
54	GFUS	GDP-L-Fucose Synthase	Protein Coding	3
55	ST8SIA4	ST8 Alpha-N-Acetyl-Neuraminide Alpha-2,8-Sialyltransferase 4	Protein Coding	3
56	NPL	N-Acetylneuraminate Pyruvate Lyase	Protein Coding	3
57	ST8SIA2	ST8 Alpha-N-Acetyl-Neuraminide Alpha-2,8-Sialyltransferase 2	Protein Coding	3
58	ST6GALNAC5	ST6 N-Acetylgalactosaminide Alpha-2,6-Sialyltransferase 5	Protein Coding	3
59	ST6GAL2	ST6 Beta-Galactoside Alpha-2,6-Sialyltransferase 2	Protein Coding	3
60	FPGT	Fucose-1-Phosphate Guanylyltransferase	Protein Coding	3
61	ST3GAL5	ST3 Beta-Galactoside Alpha-2,3-Sialyltransferase 5	Protein Coding	3
62	GFPT2	Glutamine--Fructose-6-Phosphate Transaminase 2	Protein Coding	3
63	DPM3	Dolichyl-Phosphate Mannosyltransferase Subunit 3, Regulatory	Protein Coding	2
64	DPM1	Dolichyl-Phosphate Mannosyltransferase Subunit 1, Catalytic	Protein Coding	2
65	DPM2	Dolichyl-Phosphate Mannosyltransferase Subunit 2, Regulatory	Protein Coding	2
66	ALG3	ALG3 Alpha-1,3- Mannosyltransferase	Protein Coding	1
67	ALG10B	ALG10 Alpha-1,2-Glucosyltransferase B	Protein Coding	1
68	DPAGT1	Dolichyl-Phosphate N-Acetylglucosaminephosphotransferase 1	Protein Coding	1
69	ALG14	ALG14 UDP-N-Acetylglucosaminyltransferase Subunit	Protein Coding	1
70	ALG6	ALG6 Alpha-1,3-Glucosyltransferase	Protein Coding	1
71	ALG11	ALG11 Alpha-1,2-Mannosyltransferase	Protein Coding	1
72	ALG1	ALG1 Chitobiosyldiphosphodolichol Beta-Mannosyltransferase	Protein Coding	1
73	ALG8	ALG8 Alpha-1,3-Glucosyltransferase	Protein Coding	1
74	ALG12	ALG12 Alpha-1,6-Mannosyltransferase	Protein Coding	1
75	ALG9	ALG9 Alpha-1,2-Mannosyltransferase	Protein Coding	1
76	ALG13	ALG13 UDP-N-Acetylglucosaminyltransferase Subunit	Protein Coding	1
77	ALG10	ALG10 Alpha-1,2-Glucosyltransferase	Protein Coding	1
78	ALG2	ALG2 Alpha-1,3/1,6-Mannosyltransferase	Protein Coding	1
79	RFT1	RFT1 Glycolipid Translocator Homolog	Protein Coding	1
80	MPDU1	Mannose-P-Dolichol Utilization Defect 1	Protein Coding	1

Disorders associated with Synthesis of substrates in N-glycan biosythesis SuperPath

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Retinitis pigmentosa	Direct
2	Developmental and epileptic encephalopathy 36	Direct
3	Immunodeficiency 47	Direct
4	Congenital disorder of glycosylation, type in	Enrichment	ALG1, ALG13, ALG3, DPAGT1, NUS1, PMM2, RFT1, SRD5A3	11.06
5	Congenital myasthenic syndromes with glycosylation defect	Enrichment	ALG14, ALG2, DPAGT1, GFPT1, GMPPB	10.41
6	Muscular dystrophy	Enrichment	GMPPB, PMM2	4.35
7	Free sialic acid storage disorder	Enrichment	GNE, SLC17A5	4.24
8	Polycystic kidney disease 7	Enrichment	ALG5	3.83
9	Undetermined early-onset epileptic encephalopathy	Enrichment	DHDDS, NUS1	3.46
10	Congenital disorder of glycosylation, type iic	Enrichment	SLC35C1	3.35
11	Congenital disorder of glycosylation with defective fucosylation 2	Enrichment	FCSK	3.35
12	Anemia, congenital, nonspherocytic hemolytic, 5	Enrichment	HK1	3.35
13	Congenital disorder of glycosylation, type ib	Enrichment	MPI	3.35
14	Congenital disorder of glycosylation, type ia	Enrichment	PMM2	3.35
15	Retinitis pigmentosa 79	Enrichment	HK1	3.35
16	Neuropathy, hereditary motor and sensory, russe type	Enrichment	HK1	3.35
17	Neurodevelopmental disorder with visual defects and brain anomalies	Enrichment	HK1	3.35
18	Congenital disorder of glycosylation, type im	Enrichment	DOLK	3.29
19	Congenital disorder of glycosylation, type iaa	Enrichment	NUS1	3.29
20	Retinitis pigmentosa 59	Enrichment	DHDDS	3.29
21	Kahrizi syndrome	Enrichment	SRD5A3	3.29
22	Porokeratosis 7, multiple types	Enrichment	MVD	3.29
23	Intellectual developmental disorder, autosomal dominant 55, with seizures	Enrichment	NUS1	3.29
24	Developmental delay and seizures with or without movement abnormalities	Enrichment	DHDDS	3.29
25	Rhizomelic dysplasia, ain-naz type	Enrichment	GNPNAT1	3.23
26	Congenital disorder of glycosylation with defective fucosylation 1	Enrichment	FCSK	3.05
27	Chromosomal instability with tissue-specific radiosensitivity	Enrichment	GMPPA	3.05
28	Muscular dystrophy-dystroglycanopathy , type a, 14	Enrichment	GMPPB	3.05
29	Muscular dystrophy-dystroglycanopathy , type b, 14	Enrichment	GMPPB	3.05
30	Alacrima, achalasia, and impaired intellectual development syndrome	Enrichment	GMPPA	3.05
31	Muscular dystrophy-dystroglycanopathy , type c, 14	Enrichment	GMPPB	3.05
32	Syndromic x-linked intellectual disability 17	Enrichment	GMPPA	3.05
33	Congenital muscular dystrophy-dystroglycanopathy type a14	Enrichment	GMPPB	3.05
34	Congenital disorder of glycosylation, type 1dd	Enrichment	DHRSX	2.99
35	Congenital disorder of glycosylation, type iq	Enrichment	SRD5A3	2.99
36	Myasthenic syndrome, congenital, 12	Enrichment	GFPT1	2.93
37	Immunodeficiency 23	Enrichment	PGM3	2.93
38	Childhood-onset epilepsy syndrome	Enrichment	AMDHD2	2.93
39	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies	Enrichment	PMM1	2.88
40	Linear porokeratosis	Enrichment	MVD	2.81
41	Achalasia-addisonianism-alacrima syndrome	Enrichment	GMPPA	2.75
42	Hyper ige syndrome	Enrichment	PGM3	2.75
43	Hydrops fetalis, nonimmune	Enrichment	CTSA, NEU1	2.75
44	Porokeratosis	Enrichment	MVD	2.69
45	Congenital muscular dystrophy with intellectual disability	Enrichment	GMPPB	2.66
46	Autosomal dominant polycystic kidney disease	Enrichment	ALG5	2.66
47	Inclusion body myositis	Enrichment	GNE	2.61
48	Neuraminidase deficiency	Enrichment	NEU1	2.61
49	Sialuria	Enrichment	GNE	2.61
50	Intellectual developmental disorder, autosomal recessive 12	Enrichment	ST3GAL3	2.61
51	Congenital disorder of glycosylation, type iif	Enrichment	SLC35A1	2.61
52	Thrombocytopenia 12 with or without myopathy	Enrichment	GNE	2.61
53	Glb1-related disorders	Enrichment	GLB1	2.61
54	Cathepsin a-related arteriopathy-strokes-leukoencephalopathy	Enrichment	CTSA	2.61
55	St3gal3-cdg	Enrichment	ST3GAL3	2.61
56	Non-immune hydrops fetalis	Enrichment	CTSA, NEU1	2.59
57	Congenital muscular dystrophy with cerebellar involvement	Enrichment	GMPPB	2.58
58	Muscular dystrophy-dystroglycanopathy	Enrichment	GMPPB	2.51
59	Congenital muscular dystrophy due to dystroglycanopathy	Enrichment	GMPPB	2.51
60	Polymicrogyria, bilateral perisylvian, x-linked	Enrichment	NUS1	2.44
61	Polycystic liver disease	Enrichment	ALG8, ALG9	2.36
62	Autosomal dominant polycystic liver disease	Enrichment	ALG8, ALG9	2.36
63	Muscle eye brain disease	Enrichment	GMPPB	2.35
64	Bilateral perisylvian polymicrogyria	Enrichment	NUS1	2.33
65	Muscular dystrophy-dystroglycanopathy , type c, 15	Enrichment	DPM3	2.32
66	Congenital disorder of glycosylation, type iu	Enrichment	DPM2	2.32
67	Muscular dystrophy-dystroglycanopathy , type b, 15	Enrichment	DPM3	2.32
68	Diabetes mellitus	Enrichment	PMM2	2.31
69	Salt and pepper developmental regression syndrome	Enrichment	ST3GAL5	2.31
70	Bleeding disorder, platelet-type, 19	Enrichment	GNE	2.31
71	Galactosialidosis	Enrichment	CTSA	2.31
72	Developmental and epileptic encephalopathy 15	Enrichment	ST3GAL3	2.31
73	Salt and pepper syndrome	Enrichment	ST3GAL5	2.31
74	Glycoproteinosis	Enrichment	NEU1	2.31
75	Combined deficiency of sialidase and beta galactosidase	Enrichment	CTSA	2.31
76	Optic nerve disease	Enrichment	SRD5A3	2.29
77	Myasthenic syndrome, congenital, 4c, associated with acetylcholine receptor deficiency	Enrichment	GFPT1	2.23
78	Myasthenic syndrome, congenital, 14	Enrichment	ALG2	2.23
79	Congenital disorder of glycosylation, type ih	Enrichment	ALG8	2.23
80	Intellectual developmental disorder with epilepsy, behavioral abnormalities, and coarse facies	Enrichment	ALG14	2.23
81	Gillessen-kaesbach-nishimura syndrome	Enrichment	ALG9	2.23
82	Congenital disorder of glycosylation, type ic	Enrichment	ALG6	2.23
83	Polycystic liver disease 3 with or without kidney cysts	Enrichment	ALG8	2.23
84	Creatine phosphokinase, elevated serum	Enrichment	GMPPB	2.15
85	Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay	Enrichment	PMM2	2.15
86	Isolated elevated serum creatine phosphokinase levels	Enrichment	GMPPB	2.15
87	Gm1-gangliosidosis, type i	Enrichment	GLB1	2.14
88	Mucopolysaccharidosis, type ivb	Enrichment	GLB1	2.14
89	Gm1-gangliosidosis, type ii	Enrichment	GLB1	2.14
90	Nonaka myopathy	Enrichment	GNE	2.14
91	Spondyloepimetaphyseal dysplasia, genevieve type	Enrichment	NANS	2.14
92	Gm1-gangliosidosis, type iii	Enrichment	GLB1	2.14
93	Gm1 gangliosidosis	Enrichment	GLB1	2.14
94	Congenital myasthenic syndrome	Enrichment	GFPT1	2.08
95	Focal segmental glomerulosclerosis	Enrichment	PMM2	2.05
96	Infantile sialic acid storage disease	Enrichment	SLC17A5	2.01
97	Salla disease	Enrichment	SLC17A5	2.01
98	Myopathy, autophagic vacuolar, infantile-onset	Enrichment	GNE	2.01
99	Congenital disorder of glycosylation, type ij	Enrichment	DPAGT1	1.93
100	Congenital disorder of glycosylation, type if	Enrichment	MPDU1	1.93
101	Myasthenic syndrome, congenital, 13	Enrichment	DPAGT1	1.93
102	Myasthenic syndrome, congenital, 15	Enrichment	ALG14	1.93
103	Congenital disorder of glycosylation, type ig	Enrichment	ALG12	1.93
104	Myopathy, epilepsy, and progressive cerebral atrophy	Enrichment	ALG14	1.93
105	Dpagt1-congenital disorder of glycosylation	Enrichment	DPAGT1	1.93
106	Cone dystrophy	Enrichment	SRD5A3	1.91
107	Spondyloepiphyseal dysplasia with congenital joint dislocations	Enrichment	GLB1	1.84
108	Progressive familial intrahepatic cholestasis	Enrichment	GLB1	1.77
109	Cerebral palsy	Enrichment	PMM2	1.77
110	Wilson disease	Enrichment	ALG11	1.75
111	Congenital disorder of glycosylation, type ip	Enrichment	ALG11	1.75
112	Severe combined immunodeficiency	Enrichment	PGM3	1.71
113	Congenital disorder of glycosylation, type ik	Enrichment	ALG1	1.63
114	Long qt syndrome 2	Enrichment	ALG10B	1.63
115	Primary ovarian insufficiency	Enrichment	PMM2	1.59
116	Familial isolated dilated cardiomyopathy	Enrichment	DOLK	1.57
117	Congenital disorder of glycosylation, type id	Enrichment	ALG3	1.54
118	Congenital disorder of glycosylation, type il	Enrichment	ALG9	1.54
119	Alg9-congenital disorder of glycosylation	Enrichment	ALG9	1.54
120	Lynch syndrome	Enrichment	GNE	1.44
121	Autism	Enrichment	SRD5A3	1.44
122	Polycystic kidney disease 1 with or without polycystic liver disease	Enrichment	ALG9	1.39
123	Polycystic kidney disease 1	Enrichment	ALG9	1.39
124	Myopathy, tubular aggregate, 1	Enrichment	DPAGT1	1.34
125	Autism spectrum disorder	Enrichment	HK1	1.33
126	Nephrotic syndrome, type 1	Enrichment	ALG1	1.29
127	Congenital nervous system abnormality	Enrichment	SRD5A3	1.27
128	Nervous system disease	Enrichment	SRD5A3	1.27
129	Developmental and epileptic encephalopathy	Enrichment	ST3GAL3	1.08
130	Rare genetic intellectual disability	Enrichment	ALG13	1.07
131	Congenital myopathy	Enrichment	ALG14	0.97
132	Thrombocytopenia	Enrichment	GNE	0.96
133	Spastic ataxia	Enrichment	GLB1	0.92
134	Hereditary retinal dystrophy	Enrichment	HK1	0.91
135	Fundus dystrophy	Enrichment	HK1	0.91
136	Myopathy	Enrichment	DPM3	0.76
137	Non-syndromic x-linked intellectual disability	Enrichment	ALG13	0.72
138	Microcephaly	Enrichment	ALG13	0.29

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

Synthesis of substrates in N-glycan biosythesis

Pathway Network for Synthesis of substrates in N-glycan biosythesis

Pathway network for the Synthesis of substrates in N-glycan biosythesis SuperPath

Member Pathways for Synthesis of substrates in N-glycan biosythesis

Pathways in the Synthesis of substrates in N-glycan biosythesis SuperPath

Gene overlap in member pathways for Synthesis of substrates in N-glycan biosythesis SuperPath

Associated Genes for Synthesis of substrates in N-glycan biosythesis

Associated Disorders for Synthesis of substrates in N-glycan biosythesis

Disorders associated with Synthesis of substrates in N-glycan biosythesis SuperPath

STRING Interaction Network for Synthesis of substrates in N-glycan biosythesis

Sources for Synthesis of substrates in N-glycan biosythesis