AGXT - Gene browser

AGXT

alanine--glyoxylate aminotransferase

HCNC Approved Symbol: AGXT (HGNC:341)
Genomic Coordinates: 2:240,868,824 - 240,880,500 (2q37.3)
Synonyms: AGXT1, PH1, AGT, SPT, AGT1, TLH6, Ser-PyrAT, SPAT
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

9Patients

In total, 9 patients were diagnosed with a variant in the AGXT gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

09
Patient count

Hyperoxaluria: 5 (55.6%)
Patient Count: 5 (55.6%)
% of total patients presenting each phenotype is shown in parentheses.
5 (55.6%)
Nephrocalcinosis: 4 (44.4%)
Patient Count: 4 (44.4%)
% of total patients presenting each phenotype is shown in parentheses.
4 (44.4%)
Polycystic kidney dysplasia: 2 (22.2%)
Patient Count: 2 (22.2%)
% of total patients presenting each phenotype is shown in parentheses.
2 (22.2%)
Diabetes: 1 (11.1%)
Patient Count: 1 (11.1%)
% of total patients presenting each phenotype is shown in parentheses.
1 (11.1%)
Kidney stones: 1 (11.1%)
Patient Count: 1 (11.1%)
% of total patients presenting each phenotype is shown in parentheses.
1 (11.1%)