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Mutations identified in the SMAD3 gene.
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创建时间:
2015-12-02
相关数据集
Additional file 5 of Publisher Correction: Frugal alignment-free identification of FLT3-internal tandem duplications with FiLT3r
Additional file 5. supp file 5: results-small-k.xlsx.
DataCite Commons2024-08-13 更新140
Discovery of Candidate Disease Genes in ENU–Induced Mouse Mutants by Large-Scale Sequencing, Including a Splice-Site Mutation in Nucleoredoxin
An accurate and precisely annotated genome assembly is a fundamental requirement for functional genomic analysis. Here, the complete DNA sequence and gene annotation of mouse Chromosome 11 was used to
NIAID Data Ecosystem100
Whole genome analysis of a single family identifies a single SGK3 coding variant and multiple explanations for hairlessness in Scottish Deerhounds
This work describes the identification of a single mutation within the SGK3 gene which is responsible for a rare, compete hairless (alopecia universalis) phenotype in the Scottish Deerhound. Whole gen
NIAID Data Ecosystem60
Identification of a mutation related to fatal Foal Immunodeficiency Syndrome in the Fell and Dales pony
The lethal Mendelian disease Foal Immunodeficiency Syndrome (FIS), which manifests as B-lymphocyte immunodeficiency and progressive anaemia (Scholes et al. 1998), is a substantial threat to Fell and D
NIAID Data Ecosystem110
Mus musculus domesticus strain:JIGR/DN Genome sequencing
Whole genome sequece of JIGR/DN mouse strain identifies MFSD12 (gr/gr) mutation
NIAID Data Ecosystem70



