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Symbol
Name
ID
Ddhd2
DDHD domain containing 2
MGI:1919358
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Bowel incontinence
Urinary incontinence
Disease(s) Associated with DDHD2
hereditary spastic paraplegia 54

Mouse Phenotypes
impaired spatial learning
abnormal long-term spatial reference memory
abnormal motor coordination/balance
impaired balance
impaired coordination
short stride length
decreased vertical activity
Availability Mouse Genotype
Ddhd2tm1Crv/Ddhd2tm1Crv

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
04/09/2024
MGI 6.23
The Jackson Laboratory