Mapping Data Summary

• Symbol: Scn8a
• Name: sodium channel, voltage-gated, type VIII, alpha
• ID: MGI:103169
• Chromosome: 15

20 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Intercross	15	J:13982 Beechey CV, et al., [Linkage data, Ca and med]. Mouse News Lett. 1984;71:28
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	15	J:47259 Goodwin N, et al., An embryonic stem cell bank for producing deletion complexes in mice. MGI Direct Data Submission. 1998;
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	15	J:35462 Jones JM, et al., Close linkage of three neuronal genes on distal mouse chromosome 15. Mamm Genome. 1996 Sep;7(9):696-7
CROSS	Cross Type: Backcross	15	J:35462 Jones JM, et al., Close linkage of three neuronal genes on distal mouse chromosome 15. Mamm Genome. 1996 Sep;7(9):696-7
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	15	J:55425 Yang W, et al., Expression and genetic analysis of prtb, a gene that encodes a highly conserved proline-rich protein expressed in the brain. Dev Dyn. 1999 Jun;215(2):108-16
FISH	Band: F1	15	J:39067 Priatel JJ, et al., Isolation, characterization and inactivation of the mouse Mgat3 gene: the bisecting N-acetylglucosamine in asparagine-linked oligosaccharides appears dispensable for viability and reproduction. Glycobiology. 1997 Feb;7(1):45-56
TEXT		15	J:90095 Buchner DA, et al., Three ENU-induced neurological mutations in the pore loop of sodium channel Scn8a (Na(v)1.6) and a genetically linked retinal mutation, rd13. Mamm Genome. 2004 May;15(5):344-51
TEXT		15	J:27739 Burgess DL, et al., Mutation of a new sodium channel gene, Scn8a, in the mouse mutant 'motor endplate disease'. Nat Genet. 1995 Aug;10(4):461-5
TEXT		15	J:71615 De Repentigny Y, et al., Pathological and genetic analysis of the degenerating muscle (dmu) mouse: a new allele of Scn8a. Hum Mol Genet. 2001 Aug 15;10(17):1819-27
TEXT		15	J:71615 De Repentigny Y, et al., Pathological and genetic analysis of the degenerating muscle (dmu) mouse: a new allele of Scn8a. Hum Mol Genet. 2001 Aug 15;10(17):1819-27
TEXT		15	J:42052 Fleming MD, et al., Microcytic anaemia mice have a mutation in Nramp2, a candidate iron transporter gene. Nat Genet. 1997 Aug;16(4):383-6
TEXT-Genetic Cross		15	J:41656 Brinkmeier ML, et al., Localization of somatostatin receptor genes on mouse chromosomes 2, 11, 12, 15, and 17: correlation with growth QTLs. Genomics. 1997 Jul 1;43(1):9-14
TEXT-Genetic Cross		15	J:13700 Guenet JL, Eh and med linkage. Mouse News Lett. 1976;55:21
TEXT-Genetic Cross		15	J:78134 JAX Neuroscience Mutagenesis Facility, Heritable mouse mutants from JAX NMF ENU Mutagenesis Program. MGI Direct Data Submission. 2002;
TEXT-Genetic Cross		15	J:82238 JAX Neuroscience Mutagenesis Facility, Heritable mouse mutants from JAX NMF ENU Mutagenesis Program. MGI Direct Data Submission. 2003;
TEXT-Genetic Cross		15	J:147199 Papale LA, et al., Heterozygous mutations of the voltage-gated sodium channel SCN8A are associated with spike-wave discharges and absence epilepsy in mice. Hum Mol Genet. 2009 May 1;18(9):1633-41
TEXT-Physical Mapping		15	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		15	J:66464 Hain HS, et al., Cocaine-induced seizure thresholds: quantitative trait loci detection and mapping in two populations derived from the C57BL/6 and DBA/2 mouse strains. J Pharmacol Exp Ther. 2000 Apr;293(1):180-7
TEXT-QTL		15	J:68421 Jones BC, et al., Quantitative-trait loci analysis of cocaine-related behaviours and neurochemistry. Pharmacogenetics. 1999 Oct;9(5):607-17
TEXT-Radiation Hybrid		15	J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;