Pancreatic cancer subtypes

No Pathway Network information available for Pancreatic cancer subtypes

Pathways in the Pancreatic cancer subtypes SuperPath

#	Name	Source	Genes
1	Pancreatic cancer subtypes	WikiPathways	AGR2 AGR3 ANXA10 ANXA8L1 AREG BTNL8 CDH17 CEACAM6 CLRN3 CST6 CTSE CTSV CYP3A7 DHRS9 FAM3D FAM83A FGFBP1 GPR87 KRT15 KRT17 KRT20 KRT6A KRT6C KRT7 LEMD1 LGALS4 LY6D LYZ MYO1A PLA2G10 PRR15L REG4 S100A2 SCEL SERPINB3 SERPINB4 SLC2A1 SPINK4 SPRR1B SPRR3 ST6GALNAC1 TFF1 TFF2 TFF3 TNS4 TSPAN8 UCA1 VGLL1 VSIG2 (see all 49) (see less)

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

#	Symbol	Description	Category	# Related Pathways
1	UCA1	Urothelial Cancer Associated 1	RNA Gene	1
2	PLA2G10	Phospholipase A2 Group X	Protein Coding	1
3	ST6GALNAC1	ST6 N-Acetylgalactosaminide Alpha-2,6-Sialyltransferase 1	Protein Coding	1
4	LYZ	Lysozyme	Protein Coding	1
5	LGALS4	Galectin 4	Protein Coding	1
6	FAM83A	Family With Sequence Similarity 83 Member A	Protein Coding	1
7	REG4	Regenerating Family Member 4	Protein Coding	1
8	TSPAN8	Tetraspanin 8	Protein Coding	1
9	TFF3	Trefoil Factor 3	Protein Coding	1
10	TFF2	Trefoil Factor 2	Protein Coding	1
11	TFF1	Trefoil Factor 1	Protein Coding	1
12	SLC2A1	Solute Carrier Family 2 Member 1	Protein Coding	1
13	SERPINB4	Serpin Family B Member 4	Protein Coding	1
14	SERPINB3	Serpin Family B Member 3	Protein Coding	1
15	KRT20	Keratin 20	Protein Coding	1
16	CEACAM6	CEA Cell Adhesion Molecule 6	Protein Coding	1
17	MYO1A	Myosin IA	Protein Coding	1
18	KRT17	Keratin 17	Protein Coding	1
19	KRT15	Keratin 15	Protein Coding	1
20	KRT7	Keratin 7	Protein Coding	1
21	KRT6A	Keratin 6A	Protein Coding	1
22	AREG	Amphiregulin	Protein Coding	1
23	KRT6C	Keratin 6C	Protein Coding	1
24	CYP3A7	Cytochrome P450 Family 3 Subfamily A Member 7	Protein Coding	1
25	CTSE	Cathepsin E	Protein Coding	1
26	CST6	Cystatin E/M	Protein Coding	1
27	FAM3D	FAM3 Metabolism Regulating Signaling Molecule D	Protein Coding	1
28	ANXA10	Annexin A10	Protein Coding	1
29	AGR2	Anterior Gradient 2, Protein Disulphide Isomerase Family Member	Protein Coding	1
30	DHRS9	Dehydrogenase/Reductase 9	Protein Coding	1
31	CDH17	Cadherin 17	Protein Coding	1
32	AGR3	Anterior Gradient 3, Protein Disulphide Isomerase Family Member	Protein Coding	1
33	CTSV	Cathepsin V	Protein Coding	1
34	FGFBP1	Fibroblast Growth Factor Binding Protein 1	Protein Coding	1
35	LEMD1	LEM Domain Containing 1	Protein Coding	1
36	SCEL	Sciellin	Protein Coding	1
37	LY6D	Lymphocyte Antigen 6 Family Member D	Protein Coding	1
38	TNS4	Tensin 4	Protein Coding	1
39	CLRN3	Clarin 3	Protein Coding	1
40	BTNL8	Butyrophilin Like 8	Protein Coding	1
41	PRR15L	Proline Rich 15 Like	Protein Coding	1
42	ANXA8L1	Annexin A8 Like 1	Protein Coding	1
43	SPRR3	Small Proline Rich Protein 3	Protein Coding	1
44	SPRR1B	Small Proline Rich Protein 1B	Protein Coding	1
45	S100A2	S100 Calcium Binding Protein A2	Protein Coding	1
46	GPR87	G Protein-Coupled Receptor 87	Protein Coding	1
47	VGLL1	Vestigial Like Family Member 1	Protein Coding	1
48	SPINK4	Serine Peptidase Inhibitor Kazal Type 4	Protein Coding	1
49	VSIG2	V-Set And Immunoglobulin Domain Containing 2	Protein Coding	1

Disorders associated with Pancreatic cancer subtypes SuperPath

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Pachyonychia congenita 1	Enrichment	KRT17, KRT6A	4.12
2	Pachyonychia congenita 2	Enrichment	KRT17	2.44
3	Deafness, autosomal dominant 48	Enrichment	MYO1A	2.44
4	Stomatin-deficient cryohydrocytosis with neurologic defects	Enrichment	SLC2A1	2.44
5	Pachyonychia congenita 3	Enrichment	KRT6A	2.44
6	Steatocystoma multiplex	Enrichment	KRT17	2.44
7	Respiratory infections, recurrent, and failure to thrive with or without diarrhea	Enrichment	AGR2	2.44
8	Ectodermal dysplasia 15, hypohidrotic/hair type	Enrichment	CST6	2.44
9	Diarrhea 15, congenital	Enrichment	MYO1A	2.44
10	Palmoplantar keratoderma, nonepidermolytic, focal or diffuse	Enrichment	KRT6C	2.44
11	Epilepsy, idiopathic generalized 12	Enrichment	SLC2A1	2.44
12	Immunoglobulin light chain amyloidosis	Enrichment	LYZ	2.44
13	Amyloidosis, hereditary systemic 5	Enrichment	LYZ	2.44
14	Focal palmoplantar keratoderma	Enrichment	KRT6C	2.44
15	Epilepsy with myoclonic absences	Enrichment	SLC2A1	2.44
16	Hereditary cryohydrocytosis with reduced stomatin	Enrichment	SLC2A1	2.44
17	Dystonia 9	Enrichment	SLC2A1	2.14
18	Glut1 deficiency syndrome 1	Enrichment	SLC2A1	2.14
19	Glucose transporter type 1 deficiency syndrome	Enrichment	SLC2A1	2.14
20	Nail disorder, nonsyndromic congenital, 4	Enrichment	KRT17	1.97
21	Glut1 deficiency syndrome 2	Enrichment	SLC2A1	1.97
22	Chromosome 17q23.1-q23.2 deletion syndrome	Enrichment	SLC2A1	1.97
23	Congenital diarrhea	Enrichment	MYO1A	1.97
24	Amyloidosis, hereditary systemic 2	Enrichment	LYZ	1.75
25	Paroxysmal dystonia	Enrichment	SLC2A1	1.60
26	Alternating hemiplegia of childhood	Enrichment	SLC2A1	1.54
27	Myoclonic-atonic epilepsy	Enrichment	SLC2A1	1.49
28	Skin disease	Enrichment	KRT17	1.12
29	Developmental and epileptic encephalopathy 1	Enrichment	SLC2A1	1.06
30	Strabismus	Enrichment	SLC2A1	1.03
31	Cystic fibrosis	Enrichment	CEACAM6	0.96
32	Epilepsy	Enrichment	SLC2A1	0.87
33	Benign epilepsy with centrotemporal spikes	Enrichment	SLC2A1	0.86
34	Centralopathic epilepsy	Enrichment	SLC2A1	0.84
35	West syndrome	Enrichment	SLC2A1	0.83
36	Rare autosomal dominant non-syndromic sensorineural deafness type dfna	Enrichment	MYO1A	0.76
37	Microcephaly	Enrichment	SLC2A1	0.44

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

Pancreatic cancer subtypes

Pathway Network for Pancreatic cancer subtypes

Member Pathways for Pancreatic cancer subtypes

Pathways in the Pancreatic cancer subtypes SuperPath

Associated Genes for Pancreatic cancer subtypes

Associated Disorders for Pancreatic cancer subtypes

Disorders associated with Pancreatic cancer subtypes SuperPath

STRING Interaction Network for Pancreatic cancer subtypes

Sources for Pancreatic cancer subtypes