Mapping Data

Experiment

• Experiment
  CROSS
• Chromosome
  8
• Reference
  J:47553 Bartsch JW, et al., The protein kinase N (PKN) gene PRKCL1/Prkcl1 maps to human chromosome 19p12-p13.1 and mouse chromosome 8 with close linkage to the myodystrophy (myd) mutation. Genomics. 1998 Apr 1;49(1):129-32
• ID
  MGI:1270207

Genes

Gene	Assay Type	Description
D8Mit6	PCR amplified length variant
Pkn1	Southern analysis	Prkcl1 genomic
Junb	reported elsewhere
D8Mit51	PCR amplified length variant
Cdh1	reported elsewhere

Notes

• Reference
  Authors use Prkcl1 for locus symbol Stk3.
• Experiment
  Offspring types indicate alleles inherited from F1 parent.
  

CROSS

• Type
  Backcross, female
• Female Parent
  <b> <b> <b> <b> <b>/<s> <s> <s> <s> <s>
• Strain
  (C57BL/6J-Vps54 x SEG/1 +/+)F1
• Male Parent
  <b> <b> <b> <b> <b>/<b> <b> <b> <b> <b>
• Strain
  C57BL/6J-Vps54
• Allele 1
  b from C57BL/6J
• Allele 2
  s from Not Specified

CROSS Data

MC #mice	D8Mit6	Pkn1	Junb	D8Mit51	Cdh1
20	s	s	s	s	s
13	b	b	b	b	b
14	b	s	s	s	s
16	s	b	b	b	b
4	b	b	s	s	s
7	s	s	b	b	b
3	b	b	b	b	s
1	s	s	s	s	b
2	b	s	s	b	b
1	s	b	b	s	s

Statistics

Marker 1	Marker 2	# Recombinants	Total	% Recombinants	Std Error
D8Mit6	Pkn1	33	81	40.741	5.459
Pkn1	Junb	11	81	13.580	3.806
Junb	D8Mit51	3	81	3.704	2.098
D8Mit51	Cdh1	4	81	4.938	2.407