FOXP4 - Gene browser

FOXP4

forkhead box P4

HCNC Approved Symbol: FOXP4 (HGNC:20842)
Genomic Coordinates: 6:41,546,381 - 41,602,384 (6p21.1)
Synonyms: FLJ40908
Disease Associations: Currently, this gene is not associated with any human disease in OMIM.

1Patient

In total, 1 patient was diagnosed with a variant in the FOXP4 gene.

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

01
Patient count

Chronic kidney disease: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Developmental delay: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Dysmorphism: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Growth retardation: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Hearing loss: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)