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ARHGAP29

Rho GTPase activating protein 29

HCNC Approved Symbol
ARHGAP29 (HGNC:30207)
Genomic Coordinates
1:94,168,905 - 94,314,592 (1p22.1)
Synonyms
PARG1
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.
However, the following publication(s) suggest a possible gene disease association.
View More Disease Info
ContentsPublications
Impact of rare variants in ARHGAP29 to the etiology of oral clefts: role of loss-of-function vs missense variants.
PMID:27350171

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the ARHGAP29 gene.

Frequently observed phenotypes

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

Cleft lip/palate
 1 (100.0%)