Homo sapiens PKHD1 ciliary IPT domain containing fibrocystin/polyducti - Nucleotide

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Rare variants in PKHD1 associated with Caroli syndrome: Two case reports. [Mol Genet Genomic Med. 2022]
Rare variants in PKHD1 associated with Caroli syndrome: Two case reports.
Giacobbe C, Di Dato F, Palma D, Amitrano M, Iorio R, Fortunato G. Mol Genet Genomic Med. 2022 Aug; 10(8):e1998. Epub 2022 Jun 17.
Clinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypes. [Clin Exp Nephrol. 2022]
Clinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypes.
Ishiko S, Morisada N, Kondo A, Nagai S, Aoto Y, Okada E, Rossanti R, Sakakibara N, Nagano C, Horinouchi T, et al. Clin Exp Nephrol. 2022 Feb; 26(2):140-153. Epub 2021 Sep 18.
Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants. [Kidney Int. 2021]
Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants.
Burgmaier K, Brinker L, Erger F, Beck BB, Benz MR, Bergmann C, Boyer O, Collard L, Dafinger C, Fila M, et al. Kidney Int. 2021 Sep; 100(3):650-659. Epub 2021 Apr 30.

RefSeq alternative splicing
See 42 reference mRNA sequence splice variants for the PKHD1 gene.
RefSeq protein product
See the reference protein sequence for fibrocystin isoform 2 (NP_733842.2).

Protein
Protein sequence from Nucleotide coding region
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GenScript latest version of gene cDNA ORF Clone [GenScript latest version of g...]
GenScript latest version of gene cDNA ORF Clone
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BioProject Links for SRA (Select 1427007) (1)
BioProject
Burkholderia
Burkholderia
Burkholderia Genome sequencing and assembly

BioProject
GvpZ [Prodigiosinella confusarubida]
GvpZ [Prodigiosinella confusarubida]
gi|481048615|gb|AGJ98302.1|

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Nucleotide