SLC35A2

SLC35A2

solute carrier family 35 member A2

HCNC Approved Symbol: SLC35A2 (HGNC:11022)
Genomic Coordinates: 23:48,903,183 - 48,911,958 (Xp11.23)
Synonyms: UGAT, UGT, UGT1, UGT2, UGTL, UDP-Gal-Tr, UGALT
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the SLC35A2 gene.

Frequently observed phenotypes(Top 5 only)

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

01
Patient count

Intellectual disability: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)

Last updated: 2024-06-30