Homo sapiens polycystin 1 like 1, transient receptor potential channel - Nucleotide

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PKD1L1 Is Involved in Congenital Chylothorax. [Cells. 2024]
PKD1L1 Is Involved in Congenital Chylothorax.
Whitchurch JB, Schneider S, Hilger AC, Köllges R, Stegmann JD, Waffenschmidt L, Dyer L, Thiele H, Dhabhai B, Dakal TC, et al. Cells. 2024 Jan 12; 13(2). Epub 2024 Jan 12.
A novel nonsense PKD1L1 variant cause heterotaxy syndrome with congenital asplenia in a Han Chinese patient. [J Hum Genet. 2022]
A novel nonsense PKD1L1 variant cause heterotaxy syndrome with congenital asplenia in a Han Chinese patient.
Gu H, Yuan ZZ, Xie XH, Yang YF, Tan ZP. J Hum Genet. 2022 Oct; 67(10):573-577. Epub 2022 Jun 13.
Hydrops fetalis in PKD1L1-related heterotaxy: Report of two foetuses and expanding the phenotypic and molecular spectrum. [Ann Hum Genet. 2021]
Hydrops fetalis in PKD1L1-related heterotaxy: Report of two foetuses and expanding the phenotypic and molecular spectrum.
Correa ARE, Endrakanti M, Naini K, Kabra M, Gupta N. Ann Hum Genet. 2021 May; 85(3-4):138-145. Epub 2021 Mar 2.

RefSeq alternative splicing
See 3 reference mRNA sequence splice variants for the PKD1L1 gene.
RefSeq protein product
See the reference protein sequence for polycystin-1-like protein 1 (NP_612152.1).

Protein
Protein sequence from Nucleotide coding region
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GenScript latest version of gene cDNA ORF Clone [GenScript latest version of g...]
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Nucleotide