Varaico: Literature-Extracted Genetic Variants

Gene:DYNC2H1
Variant:p.Q1537R
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DYNC2H1

NM_001377.3:p.Q1537R

Associated Papers

Genetic variations in the DYNC2H1 gene causing SRTD3 (short-rib thoracic dysplasia 3 with or without polydactyly).

Chen W et al.

Frontiers in Genetics, 2023

Targeted gene panel sequencing prenatally detects two novel mutations of DYNC2H1 in a fetus with increased biparietal diameter and polyhydramnios.

Deng L et al.

Birth Defects Research, 2018

Prenatal diagnosis of short-rib polydactyly syndrome type III or short-rib thoracic dysplasia 3 with or without polydactyly (SRTD3) associated with compound heterozygous mutations in DYNC2H1 in a fetus.

Chen CP et al.

Taiwanese Journal of Obstetrics & Gynecology, 2018

Identification of novel DYNC2H1 mutations associated with short rib-polydactyly syndrome type III using next-generation panel sequencing.

Chen LS et al.

Genetics and Molecular Research : Gmr, 2016

Targeted next-generation sequencing identifies novel compound heterozygous mutations of DYNC2H1 in a fetus with short rib-polydactyly syndrome, type III.

Mei L et al.

Clinica Chimica Acta; International Journal of Clinical Chemistry, 2015

Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement.

Schmidts M et al.

Journal of Medical Genetics, 2013

Asphyxiating thoracic dysplasia: clinical and molecular review of 39 families.

Baujat G et al.

Journal of Medical Genetics, 2013

Prenatal diagnosis and molecular genetic analysis of short rib-polydactyly syndrome type III (Verma-Naumoff) in a second-trimester fetus with a homozygous splice site mutation in intron 4 in the NEK1 gene.

Chen CP et al.

Taiwanese Journal of Obstetrics & Gynecology, 2012

Short rib-polydactyly syndrome type II (Majewski): prenatal diagnosis, perinatal imaging findings and molecular analysis of the NEK1 gene.

Chen CP et al.

Taiwanese Journal of Obstetrics & Gynecology, 2012

DYNC2H1 mutations cause asphyxiating thoracic dystrophy and short rib-polydactyly syndrome, type III.

Dagoneau N et al.

American Journal of Human Genetics, 2009

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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."