Symbol Name ID |
Shank2
SH3 and multiple ankyrin repeat domains 2 MGI:2671987 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | EEG abnormality |
Abnormal nonverbal communicative behavior |
Delayed speech and language development |
Lack of spontaneous play |
Impaired ability to form peer relationships |
Autism |
Inflexible adherence to routines |
Motor stereotypy |
Restrictive behavior |
Intellectual disability |
Seizure |
Disease(s) Associated with SHANK2 | |||||||||||
autistic disorder |
Mouse Phenotypes | nervous system phenotype |
abnormal cerebellar molecular layer |
abnormal dendritic spine morphology |
abnormal excitatory synapse morphology |
abnormal nervous system physiology |
abnormal excitatory postsynaptic potential |
enhanced long-term potentiation |
reduced long-term potentiation |
abnormal miniature excitatory postsynaptic currents |
reduced long-term depression |
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Availability | Mouse Genotype | ||||||||||
Shank2tm1.1Tmb/Shank2tm1.1Tmb | |||||||||||
Shank2tm1Mgle/Shank2tm1Mgle | * | ||||||||||
Shank2tm1.1Tmb/Shank2+ | |||||||||||
Shank2tm1.1Bcgen/Shank2tm1.1Bcgen Tg(Pcp2-cre)2Mpin/0 (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 04/16/2024 MGI 6.23 |
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