Mapping Data

Experiment

• Experiment
  TEXT-Genetic Cross
• Chromosome
  5
• Reference
  J:61187 Gwynn B, et al., Defects in the cappuccino (cno) gene on mouse chromosome 5 and human 4p cause Hermansky-Pudlak syndrome by an AP-3-independent mechanism. Blood. 2000 Dec 15;96(13):4227-35
• ID
  MGI:1929247

Genes

Gene	Assay Type
D5Mit148
D5Mit126
D5Mit352
D5Mit4
Mxd4
Hmx1
Adra2c
Add1
Lrpap1
D5Mit76
D5Mit149
D5Mit75
D5Mit288
D5Ertd521e
Bloc1s4	visible phenotype
D5Mit230
Drd5
Crmp1
D5Mit351
D5Mit127
D5Mit390
D5Mit353

Notes

• Experiment
  The authors analyzed 525 homozygous F2 cno/cno mice derived from a C3H/HeJ-cno/cno x CAST/Ei intercross. The cno mutation was mapped to Chromosome 5 and the order/distance of markers was: D5Mit148 - 0.8 +/- 0.3 cM - D5Mit126, D5Mit352, D5Mit4, Mad4, Hmx1, Adra2c, Add1, Lrpap1 - 0.2 +/- 0.1 cM - D5Mit46 - 0.5 +/- 0.2 cM - D5Mit149 - 0.3 +/- 0.2 cM - D5Mit75 - 0.2 +/- 0.1 cM - D5Mit288 - 0.5 +/- 0.1 cM - D5ERTD521E - 0.3 +/- 0.2 CM - CNO - 0.6 +/- 0.2 CM - D5Mit320 - 0.2 +/- 0.1 cM - Drd5, Crmp1, D5Mit351,D5Mit127, D5Mit390 - 1.1 +/- 0.3 cM - D5Mit353.