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WLS

Wnt ligand secretion mediator

HCNC Approved Symbol
WLS (HGNC:30238)
Genomic Coordinates
1:68,098,459 - 68,232,546 (1p31.3)
Synonyms
FLJ23091, MRP, EVI, mig-14, C1orf139, GPR177
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 WLS gene.

Frequently observed phenotypes

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

Abnormal facial shape
 1 (100.0%)
Growth delay
 1 (100.0%)
Intellectual disability
 1 (100.0%)
Open mouth
 1 (100.0%)
Protruding ear
 1 (100.0%)
WLS - Gene browser | 3billion