Mapping Data

Experiment

• Experiment
  CROSS
• Chromosome
  3
• Reference
  J:53340 Sprunger LK, et al., Dystonia associated with mutation of the neuronal sodium channel Scn8a and identification of the modifier locus Scnm1 on mouse chromosome 3. Hum Mol Genet. 1999 Mar;8(3):471-9
• ID
  MGI:1341409

Genes

Gene	Assay Type
D3Mit6
D3Mit227
D3Mit137
D3Mit40
Scnm1	visible phenotype
D3Mit141
D3Mit101
D3Mit11
D3Mit189
D3Mit42
D3Mit351

CROSS

• Type
  Intercross
• Female Parent
  <b> <b> <b> <b> <b> <b> <b> <b> <b> <b> <b/<b> <b> <b> <b> <b> <b> <b> <b> <b> <b> <b
• Strain
  C57BL/6J-Scn8a
• Male Parent
  <c> <c> <c> <c> <c> <c> <c> <c> <c> <c> <c>/<c> <c> <c> <c> <c> <c> <c> <c> <c> <c> <c>
• Strain
  C3HeB/FeJ
• Allele 1
  b from C57BL/6J
• Allele 2
  c from C3HeB/FeJ

2x2 Data Reported

Marker 1	Marker 2	# Recombinants	# Parentals
D3Mit6	D3Mit137	12	80
D3Mit227	D3Mit137	12	80
D3Mit137	D3Mit40	6	156
D3Mit40	Scnm1	8	244
D3Mit40	D3Mit141	8	244
Scnm1	D3Mit101	3	235
D3Mit141	D3Mit101	3	235
D3Mit101	D3Mit11	4	220
D3Mit11	D3Mit189	2	126
D3Mit189	D3Mit42	15	119
D3Mit42	D3Mit351	10	124