increased stereotypic behavior Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description more frequent incidence of repetitive, invariant, perseverative motor patterns that do not appear to be purposeful (Mammalian Phenotype Ontology, MP_0001409)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001409
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Genes

19 gene mutations causing the increased stereotypic behavior phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADGRL3 adhesion G protein-coupled receptor L3
CACNA1C calcium channel, voltage-dependent, L type, alpha 1C subunit
CNTNAP2 contactin associated protein-like 2
DRD3 dopamine receptor D3
EIF4EBP2 eukaryotic translation initiation factor 4E binding protein 2
FEZ1 fasciculation and elongation protein zeta 1 (zygin I)
FMR1 fragile X mental retardation 1
GRXCR1 glutaredoxin, cysteine rich 1
HCN2 hyperpolarization activated cyclic nucleotide gated potassium channel 2
HTRA2 HtrA serine peptidase 2
IMPA1 inositol(myo)-1(or 4)-monophosphatase 1
MECP2 methyl CpG binding protein 2
SHANK2 SH3 and multiple ankyrin repeat domains 2
SHANK3 SH3 and multiple ankyrin repeat domains 3
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3
SYNGAP1 synaptic Ras GTPase activating protein 1
TNC tenascin C
TSHR thyroid stimulating hormone receptor
ZDHHC17 zinc finger, DHHC-type containing 17