Symbol Name ID |
Frmd5
FERM domain containing 5 MGI:2442557 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Feeding difficulties |
Urinary incontinence |
Disease(s) Associated with FRMD5 | ||
neurodevelopmental disorder with eye movement abnormalities and ataxia |
Mouse Phenotypes | behavior/neurological phenotype |
abnormal spatial reference memory |
abnormal emotion/affect behavior |
abnormal response to novel object |
increased grooming behavior |
decreased grip strength |
increased vertical activity |
hyperactivity |
impaired social recognition |
decreased social investigation |
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Availability | Mouse Genotype | ||||||||||
Frmd5em#Yuw/Frmd5em#Yuw | * | ||||||||||
Frmd5tm1a(EUCOMM)Hmgu/Frmd5tm1a(EUCOMM)Hmgu | |||||||||||
Frmd5tm1b(EUCOMM)Hmgu/Frmd5tm1b(EUCOMM)Hmgu |
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 08/02/2024 MGI 6.24 |
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