Iminoglycinuria (IG)

Alias:

Iminoglycinuria, Digenic

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Iminoglycinuria, also known as ig, is related to hyperglycinuria and aminoaciduria. An important gene associated with Iminoglycinuria is SLC36A2 (Solute Carrier Family 36 Member 2), and among its related pathways/superpathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Nuclear receptors meta-pathway. Affiliated tissues include kidney and eye, and related phenotypes are prolinuria and hydroxyprolinuria

Related ID：

MALACARDS：IMN001

OMIM：242600

MESH：C536285