Rapoport-Luebering glycolytic shunt

No Pathway Network information available for Rapoport-Luebering glycolytic shunt

#	Name	Source	Genes
1	Rapoport-Luebering glycolytic shunt	PubChem	BPGM MINPP1 PGAM1 PGAM2

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

#	Symbol	Description	Category	# Related Pathways
1	MINPP1	Multiple Inositol-Polyphosphate Phosphatase 1	Protein Coding	1
2	PGAM2	Phosphoglycerate Mutase 2	Protein Coding	1
3	PGAM1	Phosphoglycerate Mutase 1	Protein Coding	1
4	BPGM	Bisphosphoglycerate Mutase	Protein Coding	1

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Erythrocytosis, familial, 8	Enrichment	BPGM	3.53
2	Autosomal recessive secondary polycythemia not associated with vhl gene	Enrichment	BPGM	3.53
3	Pontocerebellar hypoplasia, type 7	Enrichment	MINPP1	3.23
4	Pontocerebellar hypoplasia, type 16	Enrichment	MINPP1	3.05
5	Familial papillary or follicular thyroid carcinoma	Enrichment	MINPP1	3.05
6	Glycogen storage disease x	Enrichment	PGAM2	2.93
7	Thyroid cancer, nonmedullary, 2	Enrichment	MINPP1	2.69
8	Follicular thyroid carcinoma	Enrichment	MINPP1	2.69
9	Pontocerebellar hypoplasia	Enrichment	MINPP1	2.28

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 Rapoport-Luebering glycolytic shunt