Mapping Data

Experiment

• Experiment
  CROSS
• Chromosome
  13
• Reference
  J:37707 Scharf JM, et al., The mouse region syntenic for human spinal muscular atrophy lies within the Lgn1 critical interval and contains multiple copies of Naip exon 5. Genomics. 1996 Dec 15;38(3):405-17
• ID
  MGI:48359

Genes

Gene	Assay Type	Description
D13Mit27	PCR amplified length variant
Dhfr	reported elsewhere
D13Mit104	PCR amplified length variant
D13Mit37	PCR amplified length variant
Smn1	SSCP	JMS6, JMS7
Etfa	reported elsewhere

Notes

• Experiment
  Detailed mapping data for markers segregating in this cross is associated with the JAX (BSS) mapping panel, accessible by clicking on the JAX link highlighted below.Offspring types indicate alleles inherited from F1 parent.
  F1 direction known.
  

CROSS

• Type
  Backcross, female
• Female Parent
  <b> <b> <b> <b> <b> <b>/<s> <s> <s> <s> <s> <s>
• Strain
  (C57BL/6JEi x SPRET/Ei)F1
• Male Parent
  <s> <s> <s> <s> <s> <s>/<s> <s> <s> <s> <s> <s>
• Strain
  SPRET/EiJ
• Mapping Panel
  JAX (BSS)
• Allele 1
  b from C57BL/6JEiJ
• Allele 2
  s from SPRET/EiJ

CROSS Data

MC #mice	D13Mit27	Dhfr	D13Mit104	D13Mit37	Smn1	Etfa
1	b	b	s	s	s	s

Statistics

Marker 1	Marker 2	# Recombinants	Total	% Recombinants	Std Error
D13Mit27	Dhfr	0	1	0.000	0.000
Dhfr	D13Mit104	1	1	100.000	0.000
D13Mit104	D13Mit37	0	1	0.000	0.000
D13Mit37	Smn1	0	1	0.000	0.000
Smn1	Etfa	0	1	0.000	0.000