Model Description: These mice carry loxP sites flanking target exons of Cdyl gene. When crossed with a Cre recombinase-expressing strain, this strain is useful in eliminating tissue-specific conditional expression of Cdyl gene.
Official Symbol: Cdyl
NCBI ID: 12593
MGI ID: 1339956
Ensembl ID: ENSMUSG00000059288
Pubmed: Cdyl
Human Ortholog: CDYL
Nomenclature
C57BL/6JSmoc-Cdylem1(flox)Smoc
Exon
Exon s
Disease
Epilepsy
Disease
Nervous System Disease
KI/KO Gene
Cdyl
Notes
Note: The expected phenotype(s) may be observed in the above-mentioned mice that bred with Emx1-Cre mice.
Synonyms
AI325931
Reference
Alison M. Muir, Yinshi Ren, Delana Hopkins Butz, Nicholas A. Davis, Robert D. Blank, David E. Birk, Se-Jin Lee, David Rowe, Jian Q. Feng, Daniel S. Greenspan, Induced ablation of Bmp1 and Tll1 produces osteogenesis imperfecta in mice. Hum Mol Genet . 2014 Jun 15;23(12):3085-101. Qin R, Cao S, Lyu T, Qi C, Zhang W, Wang Y, CDYL Deficiency Disrupts Neuronal Migration and Increases Susceptibility to Epilepsy. Cell Rep. 2017 Jan 10;18(2):380-390