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Gene BrowserrightAP1G1

AP1G1

adaptor related protein complex 1 subunit gamma 1

HCNC Approved Symbol
AP1G1 (HGNC:555)
Genomic Coordinates
16:71,729,000 - 71,808,834 (16q22.2)
Synonyms
CLAPG1, ADTG
Disease Associations
This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

2Patients

Total 2 patients were diagnosed with a variant in the AP1G1 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
Developmental delay
 2(100.0%)
Patient Count: 2 (100.0%)

% of total patients presenting each phenotype is shown in parentheses.

 2(100.0%)
Seizures, focal
 1(50.0%)
Patient Count: 1 (50.0%)

% of total patients presenting each phenotype is shown in parentheses.

 1(50.0%)
Autistic traits
 1(50.0%)
Patient Count: 1 (50.0%)

% of total patients presenting each phenotype is shown in parentheses.

 1(50.0%)
Lack of speech development
 1(50.0%)
Patient Count: 1 (50.0%)

% of total patients presenting each phenotype is shown in parentheses.

 1(50.0%)
No Results
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