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MPC2 · Vinony

EntityQ18037763· pop 5· linked from 71 articles

MPC2

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protein-coding gene in the species Homo sapiens

Connections

human chromosome 1

Ensembl genome database project

glycogen storage disease I

encephalopathy due to GLUT1 deficiency

digital object identifier

keto-D-fructose

glycolytic process

Categories

Autosomal recessive disorders Genes on human chromosome 1 Inborn errors of carbohydrate metabolism Solute carrier family Transport proteins

Sources

wikipedia.externallinksexternallink

Similar entities

Discovered by embedding cosine similarity (sentence-transformers MiniLM, 384-dim).

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What links here71 pages

oxaloacetic acid

Phosphoglycerate mutase

Glyceraldehyde-3-phosphate dehydrogenase

phosphoglycerate kinase

Dihydrolipoamide dehydrogenase

glucose transporter, type 2

Pyruvate carboxylase

3-phosphoglyceraldehyde

Fructose 1,6-bisphosphatase

L-lactate dehydrogenase

pyruvate decarboxylation

glucose transporter, type 3

human chromosome 1

L-aspartic acid

L-Malate dehydrogenase

Phosphofructokinase, muscle