Symbol Name ID |
Slc25a12
solute carrier family 25 (mitochondrial carrier, Aralar), member 12 MGI:1926080 |
Darker colors indicate more annotations |
Human Phenotypes | Drooling |
Lack of spontaneous play |
Impaired ability to form peer relationships |
Autism |
Autism with high cognitive abilities |
Inflexible adherence to routines |
Motor stereotypy |
Restrictive behavior |
Disease(s) Associated with SLC25A12 | ||||||||
Asperger syndrome | ||||||||
autistic disorder | ||||||||
developmental and epileptic encephalopathy 39 |
Mouse Phenotypes | enhanced behavioral response to amphetamine |
increased anxiety-related response |
increased thigmotaxis |
limb grasping |
tremors |
impaired balance |
impaired coordination |
impaired limb coordination |
hunched posture |
abnormal gait |
increased vertical activity |
increased locomotor activity |
hyperresponsive |
convulsive seizures |
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Availability | Mouse Genotype | ||||||||||||||
Slc25a12Gt(OST123999)Lex/Slc25a12Gt(OST123999)Lex | |||||||||||||||
Slc25a12Gt(OST123999)Lex/Slc25a12+ |
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 04/30/2024 MGI 6.23 |
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