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Details
Link-It Detail - Jax Mouse Phenotype - abnormal cerebellum posterior lobe morphology
Debug Stats
  • ### Total Build Time: 30 ms 9.048 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 418 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 293 bytes
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  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 604 bytes
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  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=19 ms Completed: 19 ms rowSize= 4.080 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.183 KB
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Jax Mouse Phenotype (1)
abnormal cerebellum posterior lobe morphology MP:0009962
Definition (1)
any structural anomaly of the region of the cerebellum that is posterior to the primary fissure and anterior to the posteriolateral fissure
Synonyms (1)
"abnormal cerebellum caudal lobe morphology" EXACT
Parents (1)
img abnormal cerebellar cortex morphology MP:0004097
Children (1)
img abnormal cerebellum posterior vermis morphology MP:0000869
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036319img abnormal cerebellar cortex morphology MP:0004097
Genes (8)

Species:
human : 8
SpeciesGeneGeneIdGene NameEvidence
HumanNPC14864Niemann-Pick disease, type C1
INFERRED
HumanMSX24488msh homeobox 2
INFERRED
HumanSMAD24087SMAD family member 2
INFERRED
HumanLMX1A4009LIM homeobox transcription factor 1, alpha
INFERRED
HumanGABRB32562gamma-aminobutyric acid (GABA) A receptor, beta 3
INFERRED
HumanEN22020engrailed homeobox 2
INFERRED
HumanEN12019engrailed homeobox 1
INFERRED
HumanARCN1372archain 1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0009962abnormal cerebellum posterior lobe morphology0self