Search: onr:"swepub:oai:DiVA.org:oru-87753" >
Biallelic TMEM251 v...
-
Ain, Noor U.School of Biological Sciences, University of the Punjab, Lahore, Pakistan; Department of Molecular Medicine and Surgery and Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden
(author)
Biallelic TMEM251 variants in patients with severe skeletal dysplasia and extreme short stature
- Article/chapterEnglish2020
Publisher, publication year, extent ...
-
2020-11-30
-
John Wiley & Sons,2020
-
printrdacarrier
Numbers
-
LIBRIS-ID:oai:DiVA.org:oru-87753
-
https://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-87753URI
-
https://doi.org/10.1002/humu.24139DOI
-
http://kipublications.ki.se/Default.aspx?queryparsed=id:145258144URI
Supplementary language notes
-
Language:English
-
Summary in:English
Part of subdatabase
Classification
-
Subject category:ref swepub-contenttype
-
Subject category:art swepub-publicationtype
Notes
-
Funding Agencies:National Institute for Medical Research Development 940714Higher Eductation Comission Pakistan Koshish Foundation, USA Sigrid Juselius Foundation
-
Skeletal dysplasias are a heterogeneous group of disorders ranging from mild to lethal skeletal defects. We investigated two unrelated families with individuals presenting with a severe skeletal disorder. In family NMD02, affected individuals had a dysostosis multiplex-like skeletal dysplasia and severe short stature (<-8.5 SD). They manifested increasingly coarse facial features, protruding abdomens, and progressive skeletal changes, reminiscent of mucopolysaccharidosis. The patients gradually lost mobility and the two oldest affected individuals died in their twenties. The affected child in family ID01 had coarse facial features and severe skeletal dysplasia with clinical features similar to mucopolysaccharidosis. She had short stature, craniosynostosis, kyphoscoliosis, and hip-joint subluxation. She died at the age of 5 years. Whole-exome sequencing identified two homozygous variants c.133C>T; p.(Arg45Trp) and c.215dupA; p.(Tyr72Ter), respectively, in the two families, affecting an evolutionary conserved gene TMEM251 (NM_001098621.1). Immunofluorescence and confocal studies using human osteosarcoma cells indicated that TMEM251 is localized to the Golgi complex. However, p.Arg45Trp mutant TMEM251 protein was targeted less efficiently and the localization was punctate. Tmem251 knockdown by small interfering RNA induced dedifferentiation of rat primary chondrocytes. Our work implicates TMEM251 in the pathogenesis of a novel disorder and suggests its potential function in chondrocyte differentiation.
Subject headings and genre
Added entries (persons, corporate bodies, meetings, titles ...)
-
Muhammad, NiazSchool of Biological Sciences, University of the Punjab, Lahore, Pakistan
(author)
-
Dianatpour, MehdiDepartment of Medical Genetics, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran; Stem Cell Technology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran
(author)
-
Baroncelli, MartaKarolinska Institutet
(author)
-
Iqbal, MuddassarSchool of Biological Sciences, University of the Punjab, Lahore, Pakistan
(author)
-
Fard, Mohammad A. F.Persian BayanGene Research and Training Center, Shiraz, Iran
(author)
-
Bukhari, IhtishamSchool of Biological Sciences, University of the Punjab, Lahore, Pakistan
(author)
-
Ahmed, SufianSchool of Biological Sciences, University of the Punjab, Lahore, Pakistan
(author)
-
Hajipour, MassoumehPersian BayanGene Research and Training Center, Shiraz, Iran
(author)
-
Tabatabaie, ZahraPersian BayanGene Research and Training Center, Shiraz, Iran
(author)
-
Foroutan, HamidrezaLaparoscopy research center, Shiraz University of Medical Sciences, Shiraz, Iran
(author)
-
Nilsson, Ola,1970-Karolinska Institutet,Örebro universitet,Institutionen för medicinska vetenskaper,Division of pediatric endocrinology and Center for Molecular Medicine, Department of Women's and Children's Health, Karolinska Institutet and University Hospital, Stockholm, Sweden; Örebro University Hospital, Örebro, Örebro, Sweden(Swepub:oru)oann
(author)
-
Faghihi, Mohammad A.Persian BayanGene Research and Training Center, Shiraz, Iran
(author)
-
Makitie, OutiKarolinska Institutet
(author)
-
Naz, SadafSchool of Biological Sciences, University of the Punjab, Lahore, Pakistan
(author)
-
School of Biological Sciences, University of the Punjab, Lahore, Pakistan; Department of Molecular Medicine and Surgery and Center for Molecular Medicine, Karolinska Institutet, Stockholm, SwedenSchool of Biological Sciences, University of the Punjab, Lahore, Pakistan
(creator_code:org_t)
Related titles
-
In:Human Mutation: John Wiley & Sons42:1, s. 89-1011059-77941098-1004
Internet link
Find in a library
To the university's database
- By the author/editor
-
Ain, Noor U.
-
Muhammad, Niaz
-
Dianatpour, Mehd ...
-
Baroncelli, Mart ...
-
Iqbal, Muddassar
-
Fard, Mohammad A ...
-
show more...
-
Bukhari, Ihtisha ...
-
Ahmed, Sufian
-
Hajipour, Massou ...
-
Tabatabaie, Zahr ...
-
Foroutan, Hamidr ...
-
Nilsson, Ola, 19 ...
-
Faghihi, Mohamma ...
-
Makitie, Outi
-
Naz, Sadaf
-
show less...
- About the subject
-
- MEDICAL AND HEALTH SCIENCES
-
MEDICAL AND HEAL ...
-
and Medical Biotechn ...
-
and Medical Biotechn ...
- Articles in the publication
-
Human Mutation
- By the university
-
Örebro University
-
Karolinska Institutet