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Details
Link-It Detail - Jax Mouse Phenotype - increased stereotypic behavior
Debug Stats
  • ### Total Build Time: 38 ms 17.537 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 388 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 268 bytes
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  • CONCEPT_GENES gt=29 ms Completed: 29 ms rowSize= 12.400 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.168 KB
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Jax Mouse Phenotype (1)
increased stereotypic behavior MP:0001409
Definition (1)
more frequent incidence of repetitive, invariant, perseverative motor patterns that do not appear to be purposeful
Parents (1)
img stereotypic behavior MP:0001408
Children (2)
img increased vertical stereotypic behavior MP:0009849
img increased horizontal stereotypic behavior MP:0009848
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053866img stereotypic behavior MP:0001408
Genes (21)

Species:
human : 21
SpeciesGeneGeneIdGene NameEvidence
HumanHTRA227429HtrA serine peptidase 2
Click here to display 34 evidence detail records.
HumanCNTNAP226047contactin associated protein-like 2
Click here to display 34 evidence detail records.
HumanZDHHC1723390zinc finger, DHHC-type containing 17
INFERRED
HumanLPHN323284latrophilin 3
Click here to display 34 evidence detail records.
HumanSHANK222941SH3 and multiple ankyrin repeat domains 2
Click here to display 34 evidence detail records.
HumanFEZ19638fasciculation and elongation protein zeta 1 (zygin I)
Click here to display 34 evidence detail records.
HumanSYNGAP18831synaptic Ras GTPase activating protein 1
INFERRED
HumanTSHR7253thyroid stimulating hormone receptor
Click here to display 34 evidence detail records.
HumanSLC6A36531solute carrier family 6 (neurotransmitter transporter), member 3
Click here to display 34 evidence detail records.
HumanNR4A24929nuclear receptor subfamily 4, group A, member 2
Click here to display 34 evidence detail records.
HumanNBN4683nibrin
Click here to display 34 evidence detail records.
HumanMECP24204methyl CpG binding protein 2 (Rett syndrome)
Click here to display 34 evidence detail records.
HumanIMPA13612inositol(myo)-1(or 4)-monophosphatase 1
INFERRED
HumanTNC3371tenascin C
Click here to display 34 evidence detail records.
HumanFMR12332fragile X mental retardation 1
Click here to display 34 evidence detail records.
HumanTOR1A1861torsin family 1, member A (torsin A)
Click here to display 34 evidence detail records.
HumanDRD31814dopamine receptor D3
Click here to display 34 evidence detail records.
HumanDBH1621dopamine beta-hydroxylase (dopamine beta-monooxygenase)
Click here to display 34 evidence detail records.
HumanCACNA1C775calcium channel, voltage-dependent, L type, alpha 1C subunit
Click here to display 34 evidence detail records.
HumanHCN2610hyperpolarization activated cyclic nucleotide-gated potassium channel 2
Click here to display 34 evidence detail records.
HumanADM133adrenomedullin
Click here to display 34 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001409increased stereotypic behavior0self