About   Help   FAQ
Symbol
Name
ID
Slc25a12
solute carrier family 25 (mitochondrial carrier, Aralar), member 12
MGI:1926080
Phenotype annotations related to behavior/neurological
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
Availability Mouse Genotype
Slc25a12Gt(OST123999)Lex/Slc25a12Gt(OST123999)Lex
Slc25a12Gt(OST123999)Lex/Slc25a12+

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
04/30/2024
MGI 6.23
The Jackson Laboratory