Searching across hundreds of databases

Our searching services are busy right now. Your search will reload in five seconds.

X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

The First Scube3 Mutant Mouse Line with Pleiotropic Phenotypic Alterations.

Helmut Fuchs | Sibylle Sabrautzki | Gerhard K H Przemeck | Stefanie Leuchtenberger | Bettina Lorenz-Depiereux | Lore Becker | Birgit Rathkolb | Marion Horsch | Lillian Garrett | Manuela A Östereicher | Wolfgang Hans | Koichiro Abe | Nobuho Sagawa | Jan Rozman | Ingrid L Vargas-Panesso | Michael Sandholzer | Thomas S Lisse | Thure Adler | Juan Antonio Aguilar-Pimentel | Julia Calzada-Wack | Nicole Ehrhard | Ralf Elvert | Christine Gau | Sabine M Hölter | Katja Micklich | Kristin Moreth | Cornelia Prehn | Oliver Puk | Ildiko Racz | Claudia Stoeger | Alexandra Vernaleken | Dian Michel | Susanne Diener | Thomas Wieland | Jerzy Adamski | Raffi Bekeredjian | Dirk H Busch | John Favor | Jochen Graw | Martin Klingenspor | Christoph Lengger | Holger Maier | Frauke Neff | Markus Ollert | Tobias Stoeger | Ali Önder Yildirim | Tim M Strom | Andreas Zimmer | Eckhard Wolf | Wolfgang Wurst | Thomas Klopstock | Johannes Beckers | Valerie Gailus-Durner | Martin Hrabé de Angelis
G3 (Bethesda, Md.) | 2016

The vertebrate Scube (Signal peptide, CUB, and EGF-like domain-containing protein) family consists of three independent members, Scube1-3, which encode secreted cell surface-associated membrane glycoproteins. Limited information about the general function of this gene family is available, and their roles during adulthood. Here, we present the first Scube3 mutant mouse line (Scube3N294K/N294K), which clearly shows phenotypic alterations by carrying a missense mutation in exon 8, and thus contributes to our understanding of SCUBE3 functions. We performed a detailed phenotypic characterization in the German Mouse Clinic (GMC). Scube3N294K/N294K mutants showed morphological abnormalities of the skeleton, alterations of parameters relevant for bone metabolism, changes in renal function, and hearing impairments. These findings correlate with characteristics of the rare metabolic bone disorder Paget disease of bone (PDB), associated with the chromosomal region of human SCUBE3 In addition, alterations in energy metabolism, behavior, and neurological functions were detected in Scube3N294K/N294K mice. The Scube3N294K/N294K mutant mouse line may serve as a new model for further studying the effect of impaired SCUBE3 gene function.

Pubmed ID: 27815347 RIS Download

Associated grants

None

Publication data is provided by the National Library of Medicine ® and PubMed ®. Data is retrieved from PubMed ® on a weekly schedule. For terms and conditions see the National Library of Medicine Terms and Conditions.

This is a list of tools and resources that we have found mentioned in this publication.


PROVEAN (tool)

RRID:SCR_002182

A software tool which predicts whether an amino acid substitution or indel has an impact on the biological function of a protein.

View all literature mentions

Jackson Laboratory (tool)

RRID:SCR_004633

An independent, nonprofit organization focused on mammalian genetics research to advance human health. Their mission is to discover the genetic basis for preventing, treating, and curing human disease, and to enable research for the global biomedical community. Jackson Laboratory breeds and manages colonies of mice as resources for other research institutions and laboratories, along with providing software and techniques. Jackson Lab also conducts genetic research and provides educational material for various educational levels.

View all literature mentions

QIAGEN (tool)

RRID:SCR_008539

A commercial organization which provides assay technologies to isolate DNA, RNA, and proteins from any biological sample. Assay technologies are then used to make specific target biomolecules, such as the DNA of a specific virus, visible for subsequent analysis.

View all literature mentions

PolyPhen: Polymorphism Phenotyping (tool)

RRID:SCR_013200

Software tool which predicts possible impact of amino acid substitution on structure and function of human protein using straightforward physical and comparative considerations. PolyPhen-2 is new development of PolyPhen tool for annotating coding nonsynonymous SNPs.

View all literature mentions

PolyPhen: Polymorphism Phenotyping (tool)

RRID:SCR_013189

Software tool which predicts possible impact of amino acid substitution on structure and function of human protein using straightforward physical and comparative considerations. PolyPhen-2 is new development of PolyPhen tool for annotating coding nonsynonymous SNPs.

View all literature mentions

C57BL/6J (tool)

RRID:IMSR_JAX:000664

Mus musculus with name C57BL/6J from IMSR.

View all literature mentions

C3HeB/FeJ (tool)

RRID:IMSR_JAX:000658

Mus musculus with name C3HeB/FeJ from IMSR.

View all literature mentions