TRRAP - Gene browser

TRRAP

transformation/transcription domain associated protein

HCNC Approved Symbol: TRRAP (HGNC:12347)
Genomic Coordinates: 7:98,878,532 - 99,013,241 (7q22.1)
Synonyms: TR-AP, PAF400, Tra1
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

20Patients

In total, 20 patients were diagnosed with a variant in the TRRAP gene.

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

020
Patient count

Global developmental delay: 7 (35.0%)
Patient Count: 7 (35.0%)
% of total patients presenting each phenotype is shown in parentheses.
7 (35.0%)
Facial dysmorphism: 5 (25.0%)
Patient Count: 5 (25.0%)
% of total patients presenting each phenotype is shown in parentheses.
5 (25.0%)
Failure to thrive: 4 (20.0%)
Patient Count: 4 (20.0%)
% of total patients presenting each phenotype is shown in parentheses.
4 (20.0%)
Microcephaly: 3 (15.0%)
Patient Count: 3 (15.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (15.0%)
Hypertelorism: 3 (15.0%)
Patient Count: 3 (15.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (15.0%)