Symbol Name ID |
Slc6a4
solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 MGI:96285 |
Darker colors indicate more annotations |
Human Phenotypes | Anosmia |
EEG abnormality |
Abnormal nonverbal communicative behavior |
Delayed speech and language development |
Lack of spontaneous play |
Impaired ability to form peer relationships |
Autism |
Addictive alcohol use |
Hyperactivity |
Attention deficit hyperactivity disorder |
Inflexible adherence to routines |
Motor stereotypy |
Restrictive behavior |
Intellectual disability |
Excessive daytime somnolence |
Obstructive sleep apnea |
Snoring |
Seizure |
Focal impaired awareness seizure |
Disease(s) Associated with SLC6A4 | |||||||||||||||||||
alcohol dependence | |||||||||||||||||||
attention deficit hyperactivity disorder | |||||||||||||||||||
autistic disorder | |||||||||||||||||||
obstructive sleep apnea |
Mouse Phenotypes | abnormal enteric nervous system morphology |
abnormal enteric neuron morphology |
abnormal brain morphology |
increased brain weight |
abnormal barrel cortex morphology |
abnormal neurite morphology |
abnormal serotonergic neuron morphology |
abnormal nervous system electrophysiology |
abnormal action potential |
abnormal neuron physiology |
abnormal neurotransmitter uptake |
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Availability | Mouse Genotype | |||||||||||
Slc6a4tm1.1Rbl/Slc6a4tm1.1Rbl | ||||||||||||
Slc6a4tm1Grch/Slc6a4tm1Grch | ||||||||||||
Slc6a4tm1Kpl/Slc6a4tm1Kpl | ||||||||||||
Slc6a4tm2.1Rbl/Slc6a4tm2.1Rbl | ||||||||||||
Slc6a4tm1Kpl/Slc6a4+ |
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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