Mapping Data Summary

• Symbol: Cacna1a
• Name: calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
• ID: MGI:109482
• Chromosome: 8

17 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Intercross	8	J:38910 Doyle J, et al., Mutations in the Cacnl1a4 calcium channel gene are associated with seizures, cerebellar degeneration, and ataxia in tottering and leaner mutant mice. Mamm Genome. 1997 Feb;8(2):113-20
CROSS	Cross Type: Backcross	8	J:38910 Doyle J, et al., Mutations in the Cacnl1a4 calcium channel gene are associated with seizures, cerebellar degeneration, and ataxia in tottering and leaner mutant mice. Mamm Genome. 1997 Feb;8(2):113-20
CROSS	Cross Type: Backcross	8	J:262 GREEN MC, et al., Tottering--a neuromusclar mutation in the mouse. And its linkage with oligosyndacylism. J Hered. 1962 Sep-Oct;53:233-7
CROSS	Cross Type: Backcross	8	J:262 GREEN MC, et al., Tottering--a neuromusclar mutation in the mouse. And its linkage with oligosyndacylism. J Hered. 1962 Sep-Oct;53:233-7
CROSS	Cross Type: Backcross Mapping Panel: EUCIB	8	J:48971 Grewal PK, et al., High-resolution mapping of mouse chromosome 8 identifies an evolutionary chromosomal breakpoint. Mamm Genome. 1998 Aug;9(8):603-7
CROSS	Cross Type: Intercross	8	J:14882 Oda SI, A new allele of the tottering locus, rolling mouse Nagoya, on Chromosome no. 8 in the mouse. Jpn J Genet. 1981;56(3):295-99
CROSS	Cross Type: Backcross	8	J:5143 Tsuji S, et al., Linkage of serum esterase and tottering in the mouse. J Hered. 1969 Jul-Aug;60(4):221-2
CROSS	Cross Type: Single backcross	8	J:5121 Yoon CH, Disturbances in developmental pathways leading to a neurological disorder of genetic origin, leaner, in mice. Dev Biol. 1969 Aug;20(2):158-81
TEXT		8	J:33012 Campbell DB, et al., Chromosomal localization of the neurological mouse mutations tottering (tg), Purkinje cell degeneration (pcd), and nervous (nr). Brain Res Mol Brain Res. 1996 Apr;37(1-2):79-84
TEXT		8	J:36596 Fletcher CF, et al., Absence epilepsy in tottering mutant mice is associated with calcium channel defects. Cell. 1996 Nov 15;87(4):607-17
TEXT-Genetic Cross		8	J:36596 Fletcher CF, et al., Absence epilepsy in tottering mutant mice is associated with calcium channel defects. Cell. 1996 Nov 15;87(4):607-17
TEXT-Genetic Cross		8	J:36596 Fletcher CF, et al., Absence epilepsy in tottering mutant mice is associated with calcium channel defects. Cell. 1996 Nov 15;87(4):607-17
TEXT-Genetic Cross		8	J:82238 JAX Neuroscience Mutagenesis Facility, Heritable mouse mutants from JAX NMF ENU Mutagenesis Program. MGI Direct Data Submission. 2003;
TEXT-Physical Mapping		8	J:36596 Fletcher CF, et al., Absence epilepsy in tottering mutant mice is associated with calcium channel defects. Cell. 1996 Nov 15;87(4):607-17
TEXT-Physical Mapping		8	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		8	J:99793 Mazon Pelaez I, et al., Identification of quantitative trait loci controlling cortical motor evoked potentials in experimental autoimmune encephalomyelitis: correlation with incidence, onset and severity of disease. Hum Mol Genet. 2005 Jul 15;14(14):1977-89
TEXT-QTL		8	J:88299 Nariyama M, et al., Identification of chromosomes associated with dental caries susceptibility using quantitative trait locus analysis in mice. Caries Res. 2004 Mar-Apr;38(2):79-84