Homo sapiens membrane protein, palmitoylated 2 (MAGUK p55 subfamily me - Nucleotide

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A de novo missense mutation in MPP2 confers an increased risk of Vogt-Koyanagi-Harada disease as shown by trio-based whole-exome sequencing. [Cell Mol Immunol. 2023]
A de novo missense mutation in MPP2 confers an increased risk of Vogt-Koyanagi-Harada disease as shown by trio-based whole-exome sequencing.
Liu X, Meng J, Liao X, Liu Y, Zhou Q, Xu Z, Yin S, Cao Q, Su G, He S, et al. Cell Mol Immunol. 2023 Nov; 20(11):1379-1392. Epub 2023 Oct 12.
The midnolin-proteasome pathway catches proteins for ubiquitination-independent degradation. [Science. 2023]
The midnolin-proteasome pathway catches proteins for ubiquitination-independent degradation.
Gu X, Nardone C, Kamitaki N, Mao A, Elledge SJ, Greenberg ME. Science. 2023 Aug 25; 381(6660):eadh5021. Epub 2023 Aug 25.
METTL3 protects METTL14 from STUB1-mediated degradation to maintain m(6) A homeostasis. [EMBO Rep. 2023]
METTL3 protects METTL14 from STUB1-mediated degradation to maintain m(6) A homeostasis.
Zeng ZC, Pan Q, Sun YM, Huang HJ, Chen XT, Chen TQ, He B, Ye H, Zhu SX, Pu KJ, et al. EMBO Rep. 2023 Mar 6; 24(3):e55762. Epub 2023 Jan 4.

RefSeq alternative splicing
See 22 reference mRNA sequence splice variants for the MPP2 gene.

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PREDICTED: Rattus norvegicus tripartite motif-containing 3 (Trim3), transcript v...
PREDICTED: Rattus norvegicus tripartite motif-containing 3 (Trim3), transcript variant X5, mRNA
gi|2678871665|ref|XM_039092586.2|

Nucleotide
PX domain-containing protein kinase variant, partial [Homo sapiens]
PX domain-containing protein kinase variant, partial [Homo sapiens]
gi|62088956|dbj|BAD92925.1|

Protein

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Nucleotide