CEP85L - Gene browser | 3billion

CEP85L

CEP85L

centrosomal protein 85 like

HCNC Approved Symbol: CEP85L (HGNC:21638)
Genomic Coordinates: 6:118,460,772 - 118,710,089 (6q22.31)
Synonyms: NY-BR-15, bA57K17.2, C6orf204
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the CEP85L gene.

Frequently observed phenotypes(Top 5 only)

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

01
Patient count

Infantile spasm: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Learning difficulties: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Lissencephaly: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)

Last updated: 2024-06-30

CEP85L - Gene browser | 3billion