RecName: Full=Protocadherin alpha-9; Short=PCDH-alpha-9; Flags: Precur - Protein

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Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease. [HGG Adv. 2021]
Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease.
Teekakirikul P, Zhu W, Gabriel GC, Young CB, Williams K, Martin LJ, Hill JC, Richards T, Billaud M, Phillippi JA, et al. Version 2. HGG Adv. 2021 Jul 8; 2(3). Epub 2021 Jul 29.
The Genetic Landscape of Hypoplastic Left Heart Syndrome. [Pediatr Cardiol. 2018]
The Genetic Landscape of Hypoplastic Left Heart Syndrome.
Yagi H, Liu X, Gabriel GC, Wu Y, Peterson K, Murray SA, Aronow BJ, Martin LJ, Benson DW, Lo CW. Pediatr Cardiol. 2018 Aug; 39(6):1069-1081. Epub 2018 Mar 22.
Identification of two novel PCDHA9 mutations associated with Hirschsprung's disease. [Gene. 2018]
Identification of two novel PCDHA9 mutations associated with Hirschsprung's disease.
Shen Q, Zhang H, Su Y, Wen Z, Zhu Z, Chen G, Peng L, Du C, Xie H, Li H, et al. Gene. 2018 Jun 5; 658:96-104. Epub 2018 Feb 22.

RefSeq protein
See the reference protein sequence for protocadherin alpha-9 precursor (NP_619602.1).

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ExactAntigen/Labome

RecName: Full=Protocadherin alpha-9; Short=PCDH-alpha-9; Flags: Precursor
RecName: Full=Protocadherin alpha-9; Short=PCDH-alpha-9; Flags: Precursor
gi|81916222|sp|Q91Y11.1|PCDA9_MOUSE

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