Protein sy'n cael ei godio yn y corff dynol gan y genyn PKD1 yw PKD1 a elwir hefyd yn Polycystin-1 a Polycystin 1, transient receptor potential channel interacting (Saesneg). Segment o DNA yw'r genyn, sy'n amgodio ffwythiant arbennig. Mae'r genyn yma wedi ei leoli ar yr edefyn ôl o gromosom dynol 16, band 16p13.3.[1]
Yn aml mae gan enynnau lawer o gyfystyron. Mae hyn oherwydd eu bod yn aml yn cael eu darganfod gan nifer o bobl mewn cyd-destunau gwahanol heb wybod mai'r un genynnau oeddyn nhw. Hefyd mae gan wahanol gymunedau gwyddonol safonau gwahanol ar gyfer enwi genynnau. Dyma restr o gyfystyron ar gyfer y genyn PKD1.
"Use of targeted sequence capture and high-throughput sequencing identifies a novel PKD1 mutation involved in adult polycystic kidney disease. ". Gene. 2017. PMID28870863.
"[Analysis of PKD1 gene mutation in a family affected with autosomal dominant polycystic kidney disease]. ". Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID28604956.
"Aortic dissection is associated with reduced polycystin-1 expression, an abnormality that leads to increased ERK phosphorylation in vascular smooth muscle cells. ". Eur J Histochem. 2016. PMID28076932.
"[Identification of a novel splicing mutation of PKD1 gene in a pedigree affected with autosomal dominant polycystic kidney disease]. ". Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID27984604.
"Novel association of familial testicular germ cell tumor and autosomal dominant polycystic kidney disease with PKD1 mutation.". Pediatr Blood Cancer. 2017. PMID27577987.
