ANKRD17 - Gene browser

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.

6Patients

In total, 6 patients were diagnosed with a variant in the ANKRD17 gene.

(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%)