Prune Belly Syndrome

A rare congenital syndrome occurring almost exclusively in males. It is characterized by partial or complete lack of the abdominal wall muscles, enlarged bladder, dilated ureters, hydronephrosis, and undescended testes. (NCI Thesaurus)

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PRTN3 wt Allele

Human PRTN3 wild-type allele is located in the vicinity of 19p13.3 and is approximately 7 kb in length. This allele, which encodes…

PRTN3 Gene

This gene plays a role in the growth of hematopoietic cells.

PRSS8 wt Allele

Human PRSS8 wild-type allele is located in the vicinity of 16p11.2 and is approximately 4 kb in length. This allele, which encodes…

PRSS8 Gene

This gene is involved in proteolysis in seminal fluid.

PRRX1 wt Allele

Human PRRX1 wild-type allele is located in the vicinity of 1q24 and is approximately 76 kb in length. This allele, which encodes…

PRRX1 Gene

This gene plays a role in both transcriptional regulation and muscle cell development.