Protein repair

No Pathway Network information available for Protein repair

#	Name	Source	Genes
1	Protein repair	Reactome	MSRA MSRB1 MSRB2 MSRB3 PCMT1 TXN (see all 6) (see less)
2	Sulindac metabolic pathway	WikiPathways	CYP1A2 CYP1B1 MSRA MSRB2 MSRB3

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

#	Symbol	Description	Category	# Related Pathways
1	MSRB2	Methionine Sulfoxide Reductase B2	Protein Coding	2
2	MSRB3	Methionine Sulfoxide Reductase B3	Protein Coding	2
3	MSRA	Methionine Sulfoxide Reductase A	Protein Coding	2
4	PCMT1	Protein-L-Isoaspartate (D-Aspartate) O-Methyltransferase	Protein Coding	1
5	MSRB1	Methionine Sulfoxide Reductase B1	Protein Coding	1
6	TXN	Thioredoxin	Protein Coding	1
7	CYP1B1	Cytochrome P450 Family 1 Subfamily B Member 1	Protein Coding	1
8	CYP1A2	Cytochrome P450 Family 1 Subfamily A Member 2	Protein Coding	1

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Deafness, autosomal recessive 74	Enrichment	MSRB3	3.43
2	Glaucoma 1, open angle, a	Enrichment	CYP1B1	3.13
3	Anterior segment dysgenesis 6	Enrichment	CYP1B1	3.13
4	Primary congenital glaucoma	Enrichment	CYP1B1	3.13
5	Glaucoma 3, primary infantile, b	Enrichment	CYP1B1	2.83
6	Juvenile glaucoma	Enrichment	CYP1B1	2.73
7	Glaucoma, primary open angle	Enrichment	CYP1B1	2.66
8	Anterior segment dysgenesis 5	Enrichment	CYP1B1	2.66
9	Glaucoma 3, primary congenital, a	Enrichment	CYP1B1	2.59
10	Peters-plus syndrome	Enrichment	CYP1B1	2.43
11	Anterior segment dysgenesis	Enrichment	CYP1B1	2.26
12	Schizophrenia	Enrichment	MSRA	1.67
13	Deafness, autosomal recessive	Enrichment	MSRB3	1.64
14	Autosomal recessive nonsyndromic deafness	Enrichment	MSRB3	1.63
15	Rare autosomal recessive non-syndromic sensorineural deafness type dfnb	Enrichment	MSRB3	1.49

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 Protein repair