Homo sapiens cDNA FLJ55857 complete cds, moderately similar to Non-imp - Nucleotide

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Articles about the NIPAL4 gene

Expanding the molecular and clinical spectrum of autosomal recessive congenital ichthyosis caused by pathogenic variants in NIPAL4 and PNPLA1 and evaluation of novel therapeutic interventions. [J Eur Acad Dermatol Venereol. ...]
Expanding the molecular and clinical spectrum of autosomal recessive congenital ichthyosis caused by pathogenic variants in NIPAL4 and PNPLA1 and evaluation of novel therapeutic interventions.
Rossel SVJ, Clabbers JMK, Steijlen PM, van den Akker PC, Spuls PI, Middelkamp Hup MA, van Maarle MC, Vreeburg M, Bolling MC, van Geel M, et al. J Eur Acad Dermatol Venereol. 2023 Dec; 37(12):e1405-e1409. Epub 2023 Jul 24.
EZH2 depletion potentiates MYC degradation inhibiting neuroblastoma and small cell carcinoma tumor formation. [Nat Commun. 2022]
EZH2 depletion potentiates MYC degradation inhibiting neuroblastoma and small cell carcinoma tumor formation.
Wang L, Chen C, Song Z, Wang H, Ye M, Wang D, Kang W, Liu H, Qing G. Nat Commun. 2022 Jan 10; 13(1):12. Epub 2022 Jan 10.
Expanding the clinical phenotype associated with NIPAL4 mutation: Study of a Tunisian consanguineous family with erythrokeratodermia variabilis-Like Autosomal Recessive Congenital Ichthyosis. [PLoS One. 2021]
Expanding the clinical phenotype associated with NIPAL4 mutation: Study of a Tunisian consanguineous family with erythrokeratodermia variabilis-Like Autosomal Recessive Congenital Ichthyosis.
Charfeddine C, Laroussi N, Mkaouar R, Jouini R, Khayat O, Redissi A, Mosbah A, Dallali H, Chedly Debbiche A, Zaouak A, et al. PLoS One. 2021; 16(10):e0258777. Epub 2021 Oct 20.

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Reference sequence information

RefSeq alternative splicing
See 4 reference mRNA sequence splice variants for the NIPAL4 gene.

More about the NIPAL4 gene

This gene likely encodes a membrane receptor. Mutations in this gene have been associated with autosomal recessive congenital ichthyosis. [p...
Also Known As: ARCI6, ICHTHYIN, ICHYN,...

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reagents [ExactAntigen/Labome]
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ExactAntigen/Labome

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Homo sapiens cDNA FLJ55857 complete cds, moderately similar to Non-imprinted in Prader-Willi/Angelmansyndrome region protein 2 homolog

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Articles about the NIPAL4 gene

Reference sequence information

More about the NIPAL4 gene

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