MSX2 - Gene browser | 3billion

MSX2

MSX2

msh homeobox 2

HCNC Approved Symbol: MSX2 (HGNC:7392)
Genomic Coordinates: 5:174,724,582 - 174,730,896 (5q35.2)
Synonyms: CRS2, FPP, HOX8, MSH, PFM, PFM1
Disease Associations: This gene is associated with the following 3 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the MSX2 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

Abnormal parietal bone morphology: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Calvarial skull defect: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Large fontanelles: 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

MSX2 - Gene browser | 3billion