Varaico: Literature-Extracted Genetic Variants

Gene:TWIST2
Variant:p.E75K
Back to variants list

TWIST2

NM_001271893.4:p.E75K

Associated Papers

Mechanisms of Regulation of the CHRDL1 Gene by the TWIST2 and ADD1/SREBP1c Transcription Factors.

Casasnovas-Nieves JJ et al.

Genes, 2023

Z-flipon variants reveal the many roles of Z-DNA and Z-RNA in health and disease.

Umerenkov D et al.

Life Science Alliance, 2023

37164635 (PubMed )
Supplement: LSA-2023-01962_TableS6.xlsx › Experimental_by_OMIM

Ocular adnexal phenotype and management of a patient with mosaic expression of a mutation in TWIST2.

De Niear MA et al.

Orbit (amsterdam, Netherlands), 2022

Are transient protein-protein interactions more dispensable?

Ghadie MA et al.

Plos Computational Biology, 2022

35404956 (PubMed )
Supplement: pcbi.1010013.s002.xlsx › _D__Lit-SI_disMut_edgotypes

Mutation Edgotype Drives Fitness Effect in Human.

Ghadie M et al.

Frontiers in Bioinformatics, 2021

36303776 (PubMed )
Supplement: Table2.XLSX › _D__Lit-SI_pathMt_edgotype

Laryngo-tracheal stenosis in a woman with ablepharon macrostomia syndrome.

Ciriaco P et al.

Bmc Pulmonary Medicine, 2019

Estimating dispensable content in the human interactome.

Ghadie M et al.

Nature Communications, 2019

31324802 (PubMed )
Supplement: 41467_2019_11180_MOESM6_ESM.xlsx › _B__Y2H-SI_disease_mut

Use of the Masquerade Flap in Ablepharon-Macrostomia Syndrome: A Case Report.

Hollanders K et al.

Cornea, 2018

The focal facial dermal dysplasias: phenotypic spectrum and molecular genetic heterogeneity.

Lee BH et al.

Journal of Medical Genetics, 2017

Localized TWIST1 and TWIST2 basic domain substitutions cause four distinct human diseases that can be modeled in Caenorhabditis elegans.

Kim S et al.

Human Molecular Genetics, 2017

Barber-Say syndrome and Ablepharon-Macrostomia syndrome: An overview.

De Maria B et al.

American Journal of Medical Genetics. Part A, 2016

Recurrent Mutations in the Basic Domain of TWIST2 Cause Ablepharon Macrostomia and Barber-Say Syndromes.

Marchegiani S et al.

American Journal of Human Genetics, 2015

Zellweger syndrome: first reported case in Thailand and literature review.

Jaruratanasirikul S et al.

The Southeast Asian Journal of Tropical Medicine and Public Health, 1995

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."