Dissolution of Fibrin Clot

No Pathway Network information available for Dissolution of Fibrin Clot

#	Name	Source	Genes
1	Dissolution of Fibrin Clot	Reactome	ANXA2 HRG PLAT PLAU PLAUR PLG S100A10 SERPINB2 SERPINB6 SERPINB8 SERPINE1 SERPINE2 SERPINF2 (see all 13) (see less)

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

#	Symbol	Description	Category	# Related Pathways
1	ANXA2	Annexin A2	Protein Coding	1
2	HRG	Histidine Rich Glycoprotein	Protein Coding	1
3	SERPINE1	Serpin Family E Member 1	Protein Coding	1
4	SERPINB2	Serpin Family B Member 2	Protein Coding	1
5	SERPINB6	Serpin Family B Member 6	Protein Coding	1
6	SERPINE2	Serpin Family E Member 2	Protein Coding	1
7	SERPINB8	Serpin Family B Member 8	Protein Coding	1
8	PLAT	Plasminogen Activator, Tissue Type	Protein Coding	1
9	PLAU	Plasminogen Activator, Urokinase	Protein Coding	1
10	PLAUR	Plasminogen Activator, Urokinase Receptor	Protein Coding	1
11	PLG	Plasminogen	Protein Coding	1
12	SERPINF2	Serpin Family F Member 2	Protein Coding	1
13	S100A10	S100 Calcium Binding Protein A10	Protein Coding	1

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Alpha-2-plasmin inhibitor deficiency	Enrichment	SERPINF2	3.02
2	Angioedema, hereditary, 4	Enrichment	PLG	3.02
3	Plasminogen activator inhibitor-1 deficiency	Enrichment	SERPINE1	3.02
4	Deafness, autosomal recessive 91	Enrichment	SERPINB6	3.02
5	Peeling skin syndrome 5	Enrichment	SERPINB8	3.02
6	Congenital plasminogen activator inhibitor type 1 deficiency	Enrichment	SERPINE1	3.02
7	Lethal hydranencephaly-diaphragmatic hernia syndrome	Enrichment	PLAT	3.02
8	Plasminogen deficiency, type i	Enrichment	PLG	2.72
9	Quebec platelet disorder	Enrichment	PLAU	2.72
10	Thrombophilia due to histidine-rich glycoprotein deficiency	Enrichment	HRG	2.72
11	Hereditary angioedema	Enrichment	PLG	2.72
12	Thrombophilia due to hrg deficiency	Enrichment	HRG	2.72
13	Angioedema, hereditary, 1	Enrichment	PLG	2.54
14	Peeling skin syndrome 4	Enrichment	SERPINB8	2.54
15	Peeling skin syndrome 3	Enrichment	SERPINB8	2.42
16	Pseudomyogenic hemangioendothelioma	Enrichment	SERPINE1	2.42
17	Alzheimer disease 2	Enrichment	PLAU	2.32
18	Alzheimer disease, familial, 1	Enrichment	PLAU	1.79
19	Cystic fibrosis	Enrichment	PLG	1.52
20	Rare autosomal recessive non-syndromic sensorineural deafness type dfnb	Enrichment	SERPINB6	1.09

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 Dissolution of Fibrin Clot