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AP2S1

adaptor related protein complex 2 subunit sigma 1

HCNC Approved Symbol
AP2S1 (HGNC:565)
Genomic Coordinates
19:46,838,167 - 46,850,846 (19q13.32)
Synonyms
FBHOk, FBH3, CLAPS2, HHC3
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 AP2S1 gene.

Frequently observed phenotypes

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

Hypercalcemia
 2 (100.0%)
Crowded teeth
 1 (50.0%)
Hypercalciuria
 1 (50.0%)
Learning difficulties
 1 (50.0%)
Long face
 1 (50.0%)
AP2S1 - Gene browser | 3billion