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Details
Link-It Detail - Jax Mouse Phenotype - abnormal cerebellum posterior vermis morphology
Debug Stats
  • ### Total Build Time: 66 ms 12.830 KB
  • CONCEPT_NAME gt=15 ms Completed: 15 ms rowSize= 422 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 322 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 195 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
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  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 1.049 KB
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 2.012 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.941 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=25 ms Completed: 25 ms rowSize= 4.582 KB
  • CONCEPT_XREFS gt=6 ms Completed: 6 ms rowSize= 1.185 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal cerebellum posterior vermis morphology MP:0000869
Definition (1)
any structural anomaly of the posterior portion of the narrow middle zone between the two hemispheres of the cerebellum that is located posterior to the primary fissure
Synonyms (1)
"cerebellum posterior vermis dysplasia" EXACT
Parents (2)
img abnormal cerebellum vermis morphology MP:0000864
img abnormal cerebellum posterior lobe morphology MP:0009962
Children (4)
img abnormal cerebellum vermis lobule VII morphology MP:0009995
img abnormal cerebellum vermis lobule VI morphology MP:0009994
img abnormal cerebellum vermis lobule VIII morphology MP:0009996
img abnormal cerebellum vermis lobule IX morphology MP:0009992
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363110img abnormal cerebellum vermis morphology MP:0000864
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363110img abnormal cerebellum posterior lobe morphology MP:0009962
Genes (8)

Species:
human : 8
SpeciesGeneGeneIdGene NameEvidence
HumanNPC14864Niemann-Pick disease, type C1
Click here to display 16 evidence detail records.
HumanMSX24488msh homeobox 2
INFERRED
HumanSMAD24087SMAD family member 2
INFERRED
HumanLMX1A4009LIM homeobox transcription factor 1, alpha
Click here to display 16 evidence detail records.
HumanGABRB32562gamma-aminobutyric acid (GABA) A receptor, beta 3
INFERRED
HumanEN22020engrailed homeobox 2
Click here to display 16 evidence detail records.
HumanEN12019engrailed homeobox 1
Click here to display 16 evidence detail records.
HumanARCN1372archain 1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000869abnormal cerebellum posterior vermis morphology0self