Mapping Data Summary for D13Cwr22

About Help FAQ

Mapping Data Summary

Symbol
Name
ID
Chromosome

D13Cwr22
DNA segment, Chr. 13, Case Western Reserve 22
MGI:1341305
13

Experiment Type	Details	Chromosome	Reference
TEXT-Physical Mapping		13	J:54407 Hong HK, et al., Pleiotropic skeletal and ocular phenotypes of the mouse mutation congenital hydrocephalus (ch/Mf1) arise from a winged helix/forkhead transcriptionfactor gene. Hum Mol Genet. 1999 Apr;8(4):625-37

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 11/05/2024 MGI 6.24