SLC35B2 - Gene browser | 3billion

SLC35B2

SLC35B2

solute carrier family 35 member B2

HCNC Approved Symbol: SLC35B2 (HGNC:16872)
Genomic Coordinates: 6:44,254,101 - 44,257,890 (6p21.1)
Synonyms: UGTrel4
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the SLC35B2 gene.

Frequently observed phenotypes(Top 5 only)

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

02
Patient count

Nystagmus: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)
Global development delay: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)
Generalized hypotonia: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)

Last updated: 2024-06-30

SLC35B2 - Gene browser | 3billion