About   Help   FAQ
Symbol
Name
ID
Mpzl2
myelin protein zero-like 2
MGI:1289160
Phenotype annotations related to hearing/vestibular/ear
Darker colors indicate more annotations
Human Phenotypes
Progressive sensorineural hearing impairment
Disease(s) Associated with MPZL2
autosomal recessive nonsyndromic deafness 111

Mouse Phenotypes
abnormal ear morphology
Availability Mouse Genotype
Mpzl2tm1b(EUCOMM)Hmgu/Mpzl2tm1b(EUCOMM)Hmgu

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/16/2024
MGI 6.23
The Jackson Laboratory