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hml
Spontaneous Allele Detail
Nomenclature
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
Mutation
origin
Strain of Origin:  CByJ.Cg-Foxn1nu/J
Mutation
description
Allele Type:    Spontaneous
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 10 anatomical structures
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)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
11/23/2021
MGI 6.17
The Jackson Laboratory