Mapping Data

Experiment

• Experiment
  TEXT
• Chromosome
  17
• Reference
  J:50247 Bergstrom RA, et al., Deletion mapping of the head tilt (het) gene in mice: a vestibular mutation causing specific absence of otoliths. Genetics. 1998 Oct;150(2):815-22
• ID
  MGI:1327564

Genes

Gene	Assay Type	Description
D17Mit245
D17Mit19
Nox3	visible phenotype
D17Tu1
D17Aus9
D17Leh48	Southern analysis	Tu48
D17Leh119I	Southern analysis	Tu119
D17Leh66E	Southern analysis
D17Leh66EII	Southern analysis
D17Leh119II	Southern analysis	Tu119
T	visible phenotype
D17Mit48
Qki
Tme
D17Leh66D

Notes

• Experiment
  The authors used complementation analysis with a collection of embryonic stem and germ cell induced deletions to localize Nox3 to an interval near the centromere of mouse Chromosome 17. The order of markers in this region of mouse Chromosome 17 is: D17Mit245 - D17Mit19 - D17Tu1 - D17Aus9 - D17Leh48 - D17Leh119I - D17Leh66E - D17Leh66EII - D17Leh119II - T - D17Mit48 - qk - Tme - D17Leh66D. Based on the order of markers, complementation analysis indicated that Nox3 resides between D17Mit245 and D17Tu1.