COX15 - Gene browser | 3billion

COX15

COX15

cytochrome c oxidase assembly homolog COX15

HCNC Approved Symbol: COX15 (HGNC:2263)
Genomic Coordinates: 10:99,694,293 - 99,732,127 (10q24.2)
Synonyms: CEMCOX2
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the COX15 gene.

Frequently observed phenotypes(Top 5 only)

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

02
Patient count

Failure to thrive: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)
Microcephaly: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)
Neurodevelopmental delay: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)

Last updated: 2024-06-30

COX15 - Gene browser | 3billion