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Details
Link-It Detail - Jax Mouse Phenotype - decreased Purkinje cell number
Debug Stats
  • ### Total Build Time: 578 ms 24.948 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 388 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 282 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 186 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=17 ms Completed: 17 ms rowSize= 1.020 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=43 ms Completed: 43 ms rowSize= 4.253 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=502 ms Completed: 502 ms rowSize= 17.520 KB
  • CONCEPT_XREFS gt=7 ms Completed: 7 ms rowSize= 1.168 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
decreased Purkinje cell number MP:0000880
Definition (1)
fewer than normal neuronal cells that are located in the interface of the molecular and granular layers of the cerebellar cortex
Synonyms (1)
"reduced Purkinje cell number" EXACT
Parents (2)
img decreased neuron number MP:0008948
img abnormal Purkinje cell number MP:0000878
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036317img decreased neuron number MP:0008948
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036317img abnormal Purkinje cell number MP:0000878
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363113img abnormal Purkinje cell number MP:0000878
Genes (54)

Species:
human : 54
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SpeciesGeneGeneIdGene NameEvidence
HumanCOMMD3-BMI1100532731
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HumanSUMF1285362sulfatase modifying factor 1
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HumanCADPS293664Ca++-dependent secretion activator 2
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HumanEBF264641early B-cell factor 2
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HumanLHX564211LIM homeobox 5
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HumanALS257679amyotrophic lateral sclerosis 2 (juvenile)
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HumanSCYL157410SCY1-like 1 (S. cerevisiae)
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HumanUSE155850unconventional SNARE in the ER 1 homolog (S. cerevisiae)
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HumanPI4K2A55361phosphatidylinositol 4-kinase type 2 alpha
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HumanFBXW755294F-box and WD repeat domain containing 7, E3 ubiquitin protein ligase
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HumanTRIM223321tripartite motif containing 2
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HumanAGTPBP123287ATP/GTP binding protein 1
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HumanZNF42323090zinc finger protein 423
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HumanARSG22901arylsulfatase G
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HumanPNPLA610908patatin-like phospholipase domain containing 6
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HumanCERS110715ceramide synthase 1
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HumanNPC210577Niemann-Pick disease, type C2
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HumanDNM1L10059dynamin 1-like
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HumanEI249538etoposide induced 2.4
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HumanKL9365klotho
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HumanCACNA2D29254calcium channel, voltage-dependent, alpha 2/delta subunit 2
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HumanHERC18925HECT and RLD domain containing E3 ubiquitin protein ligase family member 1
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HumanCACNA1G8913calcium channel, voltage-dependent, T type, alpha 1G subunit
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HumanSQSTM18878sequestosome 1
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HumanB4GALT28704UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 2
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XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000880decreased Purkinje cell number0self