WNT10B - Gene browser | 3billion

WNT10B

WNT10B

Wnt family member 10B

HCNC Approved Symbol: WNT10B (HGNC:12775)
Genomic Coordinates: 12:48,965,340 - 48,971,735 (12q13.12)
Synonyms: WNT-12, SHFM6
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the WNT10B 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

Postaxial polysyndactyly of foot: 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

WNT10B - Gene browser | 3billion