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LRRC32

leucine rich repeat containing 32

HCNC Approved Symbol
LRRC32 (HGNC:4161)
Genomic Coordinates
11:76,657,524 - 76,670,747 (11q13.5)
Synonyms
D11S833E, GARP
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 LRRC32 gene.

Frequently observed phenotypes

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

Cleft palate
 1 (100.0%)
Coarse facies
 1 (100.0%)
Corneal clouding
 1 (100.0%)
Eczema
 1 (100.0%)
Seizures
 1 (100.0%)
LRRC32 - Gene browser | 3billion