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Gene BrowserrightANKRD17

ANKRD17

ankyrin repeat domain 17

HCNC Approved Symbol
ANKRD17 (HGNC:23575)
Genomic Coordinates
4:73,073,376 - 73,258,798 (4q13.3)
Synonyms
GTAR, KIAA0697, FLJ22206, NY-BR-16, MASK2
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

6Patients

Total 6 patients were diagnosed with a variant in the ANKRD17 gene.

Frequently observed phenotypes (Top 5 only)

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

06
Patient count
Global developmental delay
 5(83.3%)
Patient Count: 5 (83.3%)

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

 5(83.3%)
Failure to thrive
 2(33.3%)
Patient Count: 2 (33.3%)

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

 2(33.3%)
Microcephaly
 2(33.3%)
Patient Count: 2 (33.3%)

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

 2(33.3%)
Prominent ear
 2(33.3%)
Patient Count: 2 (33.3%)

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

 2(33.3%)
2-3 or 4-5 toe syndactyly
 1(16.7%)
Patient Count: 1 (16.7%)

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

 1(16.7%)
No Results
• Last updated: 2024-06-30
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