hml
Spontaneous Allele Detail

Summary

• Symbol: hml
• Name: Hypoplasia of the membranous labyrinth; hypoplasia of the membranous labyrinth
• MGI ID: MGI:3576616
• Gene: hml Location: unknown Genetic Position: Chr10, Syntenic
• Alliance: hml page

Mutation origin

• Strain of Origin: CByJ.Cg-Foxn1^nu/J

Mutation description

• Allele Type: Spontaneous
• Inheritance: Recessive

Expression

In Structures Affected by this Mutation:

9 anatomical structure(s)

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 2 strains available Cell Lines: 0 lines available
• Carrying any hml Mutation: 2 strains or lines available

References

• Original: J:175136 Zheng QY, et al., Fine Mapping of a Deafness Mutation hml on Mouse Chromosome 10. Acad J Xian Jiaotong Univ. 2004 Jun;25(3):209-212
• All: 1 reference(s)