Varaico: Literature-Extracted Genetic Variants

Gene:MID1
Variant:p.A130T
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MID1

NM_000381.4:p.A130T

Associated Papers

Multiple molecular diagnoses identified through genome sequencing in individuals with suspected rare disease.

Malhotra A et al.

Hgg Advances, 2025

40195116 (PubMed )
Supplement: mmc1.xlsx › Multiple_molecular_diagnoses

Opitz GBBB syndrome with total anomalous pulmonary venous connection: A new MID1 gene variant.

Perea-Cabrera M et al.

Molecular Genetics & Genomic Medicine, 2023

Engineered Design of the E-Helix Structure on Ferritin Nanoparticles.

Qu Y et al.

Acs Applied Bio Materials, 2022

Structural and functional observations of the P151L MID1 mutation reveal alpha4 plays a significant role in X-linked Opitz Syndrome.

Wright KM et al.

The Febs Journal, 2017

Molecular dynamics simulation reveals insights into the mechanism of unfolding by the A130T/V mutations within the MID1 zinc-binding Bbox1 domain.

Zhao Y et al.

Plos One, 2015

MID1 catalyzes the ubiquitination of protein phosphatase 2A and mutations within its Bbox1 domain disrupt polyubiquitination of alpha4 but not of PP2Ac.

Du H et al.

Plos One, 2014

XLOS-observed mutations of MID1 Bbox1 domain cause domain unfolding.

Wright KM et al.

Plos One, 2014

Protein phosphatase 2A (PP2A)-specific ubiquitin ligase MID1 is a sequence-dependent regulator of translation efficiency controlling 3-phosphoinositide-dependent protein kinase-1 (PDPK-1).

Aranda-Orgillés B et al.

The Journal of Biological Chemistry, 2011

MID1 mutations in patients with X-linked Opitz G/BBB syndrome.

Fontanella B et al.

Human Mutation, 2008

Structure of the MID1 tandem B-boxes reveals an interaction reminiscent of intermolecular ring heterodimers.

Tao H et al.

Biochemistry, 2008

Active transport of the ubiquitin ligase MID1 along the microtubules is regulated by protein phosphatase 2A.

Aranda-Orgillés B et al.

Plos One, 2008

MID1 mutation screening in a large cohort of Opitz G/BBB syndrome patients: twenty-nine novel mutations identified.

Ferrentino R et al.

Human Mutation, 2007

Molecular dissection of the hydrophobic segments H3 and H4 of the yeast Ca2+ channel component Mid1.

Tada T et al.

The Journal of Biological Chemistry, 2003

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