MED17

MED17

mediator complex subunit 17

HCNC Approved Symbol: MED17 (HGNC:2375)
Genomic Coordinates: 11:93,784,282 - 93,814,963 (11q21)
Synonyms: CRSP77, TRAP80, DRIP80, SRB4, CRSP6
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 MED17 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

Global developmental delay: 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