rs180177173

This is a variant in the AGXT gene that changes a glycine to an arginine.

ClinVar annotation

Pathogenic★★★
4 submitters7 publications

Primary hyperoxaluria, type I (HP1)

View on ClinVar →

About AGXT

This gene is expressed only in the liver and the encoded protein is localized mostly in the peroxisomes, where it is involved in glyoxylate detoxification. Mutations in this gene, some of which alter subcellular targetting, have been associated with type I primary hyperoxaluria. [provided by RefSeq, Jul 2008]

View all AGXT variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

Community Wiki

No community notes yet for this variant. Sign in to start one.

Comments

Sign in to join the discussion.

Loading comments…