SLCO2A1 - Gene browser

SLCO2A1

solute carrier organic anion transporter family member 2A1

HCNC Approved Symbol: SLCO2A1 (HGNC:10955)
Genomic Coordinates: 3:133,932,701 - 134,029,925 (3q22.1-q22.2)
Synonyms: PGT, OATP2A1, SLC21A2, MATR1
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

24Patients

In total, 24 patients were diagnosed with a variant in the SLCO2A1 gene.

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

024
Patient count

Digital clubbing: 5 (20.8%)
Patient Count: 5 (20.8%)
% of total patients presenting each phenotype is shown in parentheses.
5 (20.8%)
Hyperhydrosis: 4 (16.7%)
Patient Count: 4 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
4 (16.7%)
Acromegaly: 4 (16.7%)
Patient Count: 4 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
4 (16.7%)
Pachydermia: 4 (16.7%)
Patient Count: 4 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
4 (16.7%)
Anemia: 3 (12.5%)
Patient Count: 3 (12.5%)
% of total patients presenting each phenotype is shown in parentheses.
3 (12.5%)