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Details
Link-It Detail - Jax Mouse Phenotype - abnormal pilomotor reflex
Debug Stats
  • ### Total Build Time: 22 ms 12.537 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 378 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 287 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 173 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=5 ms Completed: 5 ms rowSize= 570 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.902 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=15 ms Completed: 15 ms rowSize= 6.944 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.163 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal pilomotor reflex MP:0001492
Definition (1)
anomaly in the involuntary bristling of hairs that occurs when an organism is cold or experiences strong emotions such as fear or awe
Synonyms (1)
"horripilation" RELATED
Parents (1)
img abnormal reflex MP:0001961
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053866img abnormal reflex MP:0001961
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053867img abnormal reflex MP:0001961
Genes (11)

Species:
human : 11
SpeciesGeneGeneIdGene NameEvidence
HumanOPA380207optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
Click here to display 24 evidence detail records.
HumanDNM1L10059dynamin 1-like
Click here to display 24 evidence detail records.
HumanSELP6403selectin P (granule membrane protein 140kDa, antigen CD62)
Click here to display 24 evidence detail records.
HumanSELE6401selectin E
Click here to display 24 evidence detail records.
HumanSCN8A6334sodium channel, voltage gated, type VIII, alpha subunit
Click here to display 24 evidence detail records.
HumanRB15925retinoblastoma 1
Click here to display 24 evidence detail records.
HumanPTPN25771protein tyrosine phosphatase, non-receptor type 2
Click here to display 24 evidence detail records.
HumanMECP24204methyl CpG binding protein 2 (Rett syndrome)
Click here to display 24 evidence detail records.
HumanLIF3976leukemia inhibitory factor
Click here to display 24 evidence detail records.
HumanHTR2C33585-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled
Click here to display 24 evidence detail records.
HumanHFE3077hemochromatosis
Click here to display 24 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001492abnormal pilomotor reflex0self