Mapping Data Summary

• Symbol: Whrn
• Name: whirlin
• ID: MGI:2682003
• Chromosome: 4

26 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Backcross	4	J:18269 Fleming J, et al., Linkage analysis of the whirler deafness gene on mouse chromosome 4. Genomics. 1994 May 1;21(1):42-8
CROSS	Cross Type: Backcross	4	J:18269 Fleming J, et al., Linkage analysis of the whirler deafness gene on mouse chromosome 4. Genomics. 1994 May 1;21(1):42-8
CROSS	Cross Type: Backcross	4	J:269 Lane PW, Whirler mice, a recessive behavior mutation in linkage group VIII. J Hered. 1963 Nov-Dec;54:263-6
CROSS	Cross Type: Backcross	4	J:269 Lane PW, Whirler mice, a recessive behavior mutation in linkage group VIII. J Hered. 1963 Nov-Dec;54:263-6
CROSS	Cross Type: Backcross	4	J:269 Lane PW, Whirler mice, a recessive behavior mutation in linkage group VIII. J Hered. 1963 Nov-Dec;54:263-6
CROSS	Cross Type: Backcross	4	J:269 Lane PW, Whirler mice, a recessive behavior mutation in linkage group VIII. J Hered. 1963 Nov-Dec;54:263-6
CROSS	Cross Type: Backcross	4	J:269 Lane PW, Whirler mice, a recessive behavior mutation in linkage group VIII. J Hered. 1963 Nov-Dec;54:263-6
CROSS	Cross Type: Backcross	4	J:269 Lane PW, Whirler mice, a recessive behavior mutation in linkage group VIII. J Hered. 1963 Nov-Dec;54:263-6
CROSS	Cross Type: Backcross	4	J:269 Lane PW, Whirler mice, a recessive behavior mutation in linkage group VIII. J Hered. 1963 Nov-Dec;54:263-6
CROSS	Cross Type: Backcross	4	J:269 Lane PW, Whirler mice, a recessive behavior mutation in linkage group VIII. J Hered. 1963 Nov-Dec;54:263-6
CROSS	Cross Type: Single backcross	4	J:18899 Rinchik EM, Molecular genetics of the brown (b)-locus region of mouse chromosome 4. II. Complementation analyses of lethal brown deletions. Genetics. 1994 Jul;137(3):855-65
CROSS	Cross Type: Backcross	4	J:54496 Rogers MJ, et al., Genetic mapping of the whirler mutation. Mamm Genome. 1999 May;10(5):513-9
CROSS	Cross Type: Backcross	4	J:54496 Rogers MJ, et al., Genetic mapping of the whirler mutation. Mamm Genome. 1999 May;10(5):513-9
CROSS	Cross Type: Backcross	4	J:54496 Rogers MJ, et al., Genetic mapping of the whirler mutation. Mamm Genome. 1999 May;10(5):513-9
CROSS	Cross Type: Backcross	4	J:54496 Rogers MJ, et al., Genetic mapping of the whirler mutation. Mamm Genome. 1999 May;10(5):513-9
TEXT		4	J:18899 Rinchik EM, Molecular genetics of the brown (b)-locus region of mouse chromosome 4. II. Complementation analyses of lethal brown deletions. Genetics. 1994 Jul;137(3):855-65
TEXT		4	J:18898 Rinchik EM, et al., Molecular genetics of the brown (b)-locus region of mouse chromosome 4. I. Origin and molecular mapping of radiation- and chemical-induced lethal brown deletions. Genetics. 1994 Jul;137(3):845-54
TEXT-Genetic Cross		4	J:39923 British Society of Audiology short papers meeting on experimental studies of hearing and deafness. Cambridge, United Kingdom, 22-23 September 1996. Kiernan BW, et al., Analysis of the deaf mouse mutant, whirler. Br J Audiol. 1997 APR;31(2):73-132 (84-5 Abstr.)
TEXT-Genetic Cross		4	J:13477 Lane PW, New allele of diabetes. Mouse News Lett. 1968;38:24
TEXT-Genetic Cross		4	J:44122 Paige AJW, et al., Genetic and physical mapping in the vicinity of the wi locus on mouse Chromosome 4. Genet Res. 1997;70:85 (Abstr.)
TEXT-Genetic Cross		4	J:18899 Rinchik EM, Molecular genetics of the brown (b)-locus region of mouse chromosome 4. II. Complementation analyses of lethal brown deletions. Genetics. 1994 Jul;137(3):855-65
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:75900 Cryns K, et al., Vestibular dysfunction in the epistatic circler mouse is caused by phenotypic interaction of one recessive gene and three modifier genes. Genome Res. 2002 Apr;12(4):613-7
TEXT-Radiation Hybrid		4	J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;