|
Symbol Name ID |
Fa2h
fatty acid 2-hydroxylase MGI:2443327 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Bowel incontinence |
Urinary incontinence |
| Disease(s) Associated with FA2H | ||
| hereditary spastic paraplegia 35 |
| Mouse Phenotypes | behavior/neurological phenotype |
abnormal learning/memory/conditioning |
abnormal motor learning |
abnormal spatial learning |
increased freezing behavior |
impaired coordination |
decreased grip strength |
abnormal locomotor activation |
decreased vertical activity |
decreased locomotor activity |
hindlimb paralysis |
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| Availability | Mouse Genotype | |||||||||||
| Fa2hem1(IMPC)Mbp/Fa2hem1(IMPC)Mbp | ||||||||||||
| Fa2htm1.1Hama/Fa2htm1.1Hama | ||||||||||||
| Fa2htm1Meck/Fa2htm1Meck | ||||||||||||
| Fa2htm1Hama/Fa2htm1Hama Cnptm1(cre)Kan/Cnp+ (conditional) |
* | |||||||||||
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 04/23/2024 MGI 6.23 |
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