Homo sapiens phosphatidylinositol glycan anchor biosynthesis class N ( - Nucleotide

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Targeting USP10 induces degradation of oncogenic ANLN in esophageal squamous cell carcinoma. [Cell Death Differ. 2023]
Targeting USP10 induces degradation of oncogenic ANLN in esophageal squamous cell carcinoma.
Cao YF, Xie L, Tong BB, Chu MY, Shi WQ, Li X, He JZ, Wang SH, Wu ZY, Deng DX, et al. Cell Death Differ. 2023 Feb; 30(2):527-543. Epub 2022 Dec 16.
PIGN-Related Disease in Two Lithuanian Families: A Report of Two Novel Pathogenic Variants, Molecular and Clinical Characterisation. [Medicina (Kaunas). 2022]
PIGN-Related Disease in Two Lithuanian Families: A Report of Two Novel Pathogenic Variants, Molecular and Clinical Characterisation.
Siavrienė E, Maldžienė Ž, Mikštienė V, Petraitytė G, Rančelis T, Dapkūnas J, Burnytė B, Benušienė E, Sasnauskienė A, Grikinienė J, et al. Medicina (Kaunas). 2022 Oct 26; 58(11). Epub 2022 Oct 26.
Biallelic variants in PIGN cause Fryns syndrome, multiple congenital anomalies-hypotonia-seizures syndrome, and neurologic phenotypes: A genotype-phenotype correlation study. [Genet Med. 2023]
Biallelic variants in PIGN cause Fryns syndrome, multiple congenital anomalies-hypotonia-seizures syndrome, and neurologic phenotypes: A genotype-phenotype correlation study.
Loong L, Tardivo A, Knaus A, Hashim M, Pagnamenta AT, Alt K, Böhrer-Rabel H, Caro-Llopis A, Cole T, Distelmaier F, et al. Genet Med. 2023 Jan; 25(1):37-48. Epub 2022 Nov 2.

RefSeq alternative splicing
See 88 reference mRNA sequence splice variants for the PIGN gene.
RefSeq protein product
See the reference protein sequence for GPI ethanolamine phosphate transferase 1 (NP_789744.1).

Protein
Protein sequence from Nucleotide coding region
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Nucleotide