Mapping Data Summary

• Symbol: Kif12
• Name: kinesin family member 12
• ID: MGI:1098232
• Chromosome: 4

5 mapping experiments

Experiment Type	Details	Chromosome	Reference
TEXT-Congenic		4	J:243034 Mrug M, et al., Genetic and Informatic Analyses Implicate Kif12 as a Candidate Gene within the Mpkd2 Locus That Modulates Renal Cystic Disease Severity in the Cys1cpk Mouse. PLoS One. 2015;10(8):e0135678
TEXT-Physical Mapping		4	J:86904 Mburu P, et al., Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31. Nat Genet. 2003 Aug;34(4):421-8
TEXT-Physical Mapping		4	J:78475 Mouse Genome Informatics Scientific Curators, Chromosome assignment of mouse genes using the Mouse Genome Sequencing Consortium (MGSC) assembly and the ENSEMBL Database. 2002;
TEXT-Physical Mapping		4	J:80000 The FANTOM Consortium and The RIKEN Genome Exploration Research Group Phase I & II Team, Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs. Nature. 2002;420:563-573
TEXT-QTL		4	J:99468 Mrug M, et al., Kinesin family member 12 is a candidate polycystic kidney disease modifier in the cpk mouse. J Am Soc Nephrol. 2005 Apr;16(4):905-16