transmembrane protein 218 isoform 2 [Homo sapiens]

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TMEM218 dysfunction causes ciliopathies, including Joubert and Meckel syndromes. [HGG Adv. 2021]
TMEM218 dysfunction causes ciliopathies, including Joubert and Meckel syndromes.
Van De Weghe JC, Giordano JL, Mathijssen IB, Mojarrad M, Lugtenberg D, Miller CV, Dempsey JC, Mohajeri MSA, van Leeuwen E, Pajkrt E, et al. HGG Adv. 2021 Jan 14; 2(1). Epub 2020 Nov 21.
Nephronophthisis and retinal degeneration in tmem218-/- mice: a novel mouse model for Senior-Løken syndrome? [Vet Pathol. 2015]
Nephronophthisis and retinal degeneration in tmem218-/- mice: a novel mouse model for Senior-Løken syndrome?
Vogel P, Gelfman CM, Issa T, Payne BJ, Hansen GM, Read RW, Jones C, Pitcher MR, Ding ZM, DaCosta CM, et al. Vet Pathol. 2015 May; 52(3):580-95. Epub 2014 Aug 26.
The ciliary transition zone protein TMEM218 synergistically interacts with the NPHP module and its reduced dosage leads to a wide range of syndromic ciliopathies. [Hum Mol Genet. 2022]
The ciliary transition zone protein TMEM218 synergistically interacts with the NPHP module and its reduced dosage leads to a wide range of syndromic ciliopathies.
Epting D, Decker E, Ott E, Eisenberger T, Bader I, Bachmann N, Bergmann C. Hum Mol Genet. 2022 Jul 21; 31(14):2295-2306.

RefSeq mRNA
See reference mRNA sequence for the TMEM218 gene (NM_001387233.1).
RefSeq protein isoforms
See 50 reference sequence protein isoforms for the TMEM218 gene.

DNA topoisomerase IV subunit B, partial [Bradyrhizobium sp. USDA 3259]
DNA topoisomerase IV subunit B, partial [Bradyrhizobium sp. USDA 3259]
gi|357530987|gb|AET81547.1|

Protein
Homo sapiens prolyl 4-hydroxylase, transmembrane (P4HTM), transcript variant 1, ...
Homo sapiens prolyl 4-hydroxylase, transmembrane (P4HTM), transcript variant 1, mRNA
gi|1519314327|ref|NM_177939.3|

Nucleotide

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Protein