Mapping Data

Experiment

• Experiment
  TEXT
• Chromosome
  7
• Reference
  J:26849 Rinchik EM, et al., Pleiotropy in microdeletion syndromes: neurologic and spermatogenic abnormalities in mice homozygous for the p6H deletion are likely due to dysfunction of a single gene. Proc Natl Acad Sci U S A. 1995 Jul 3;92(14):6394-8
• ID
  MGI:45363

Genes

Gene	Assay Type	Description
Herc2	visible phenotype
Oca2	other	complementation

Notes

• Experiment
  EtNU induced mutations were analyzed by complementation with various p deletions. An induced mutation that result in defects in fitness, nervous/neurological functions and spermiogenesis was suggested as being caused by gene Herc2. The pleiotrophy causedby this mutation is similar to that exhibited by the p^6H/p^6H homozygous deletions. The authors indicate that Herc2 maps with D7H15F37S1 to a region of Chromosome 7 proximal to p.