Homo sapiens mRNA for MID2 protein

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Expanding the genetic and phenotypic spectrum of TRAPPC9 and MID2-related neurodevelopmental disabilities: report of two novel mutations, 3D-modelling, and molecular docking studies. [J Hum Genet. 2024]
Expanding the genetic and phenotypic spectrum of TRAPPC9 and MID2-related neurodevelopmental disabilities: report of two novel mutations, 3D-modelling, and molecular docking studies.
Kharrat M, Triki C, Ben Isaa A, Bouchaala W, Alila O, Chouchen J, Ghouliya Y, Kamoun F, Tlili A, Fakhfakh F. J Hum Genet. 2024 Jul; 69(7):291-299. Epub 2024 Mar 11.
A Degradation Motif in STAU1 Defines a Novel Family of Proteins Involved in Inflammation. [Int J Mol Sci. 2022]
A Degradation Motif in STAU1 Defines a Novel Family of Proteins Involved in Inflammation.
Gonzalez Quesada Y, DesGroseillers L. Int J Mol Sci. 2022 Sep 30; 23(19). Epub 2022 Sep 30.
Cullin 3 Exon 9 Deletion in Familial Hyperkalemic Hypertension Impairs Cullin3-Ring-E3 Ligase (CRL3) Dynamic Regulation and Cycling. [Int J Mol Sci. 2022]
Cullin 3 Exon 9 Deletion in Familial Hyperkalemic Hypertension Impairs Cullin3-Ring-E3 Ligase (CRL3) Dynamic Regulation and Cycling.
Kouranti I, Abdel Khalek W, Mazurkiewicz S, Loisel-Ferreira I, Gautreau AM, Pintard L, Jeunemaitre X, Clauser E. Int J Mol Sci. 2022 May 5; 23(9). Epub 2022 May 5.

RefSeq alternative splicing
See 4 reference mRNA sequence splice variants for the MID2 gene.

reagents [ExactAntigen/Labome]
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Order full-length cDNA clone [GeneCopoeia Inc.]
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Nucleotide