DEAF1 - Gene browser

DEAF1

DEAF1 transcription factor

HCNC Approved Symbol: DEAF1 (HGNC:14677)
Genomic Coordinates: 11:644,220 - 707,083 (11p15.5)
Synonyms: NUDR, SPN, ZMYND5
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

14Patients

In total, 14 patients were diagnosed with a variant in the DEAF1 gene.

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

014
Patient count

Global developmental delay: 6 (42.9%)
Patient Count: 6 (42.9%)
% of total patients presenting each phenotype is shown in parentheses.
6 (42.9%)
Epilepsy: 3 (21.4%)
Patient Count: 3 (21.4%)
% of total patients presenting each phenotype is shown in parentheses.
3 (21.4%)
Autism: 3 (21.4%)
Patient Count: 3 (21.4%)
% of total patients presenting each phenotype is shown in parentheses.
3 (21.4%)
Developmental delay: 3 (21.4%)
Patient Count: 3 (21.4%)
% of total patients presenting each phenotype is shown in parentheses.
3 (21.4%)
Delayed speech and language development: 3 (21.4%)
Patient Count: 3 (21.4%)
% of total patients presenting each phenotype is shown in parentheses.
3 (21.4%)