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Details
Link-It Detail - Jax Mouse Phenotype - abnormal cerebellum morphology
Debug Stats
  • ### Total Build Time: 2,027 ms 24.013 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 388 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 178 bytes
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  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 588 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 3.309 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 1.579 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=2,017 ms Completed: 2.017 Seconds rowSize= 16.332 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.168 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal cerebellum morphology MP:0000849
Definition (1)
any structural anomaly of the part of the metencephalon that lies in the posterior cranial fossa dorsal to the pons and medulla that is concerned with the coordination of movement and learning of motor skills
Synonyms (1)
"cerebellar dysplasia" EXACT
Parents (1)
img abnormal metencephalon morphology MP:0000847
Children (7)
img abnormal cerebellum deep nucleus morphology MP:0009979
img abnormal cerebellar cortex morphology MP:0004097
img absent cerebellum MP:0000850
img enlarged cerebellum MP:0008914
img small cerebellum MP:0000852
img abnormal cerebellum white matter morphology MP:0009978
img abnormal cerebellum development MP:0000854
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036317img abnormal metencephalon morphology MP:0000847
Genes (318)

Species:
human : 318
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SpeciesGeneGeneIdGene NameEvidence
HumanCOMMD3-BMI1100532731
INFERRED
HumanOCLN100506658occludin
Click here to display 214 evidence detail records.
HumanSKOR2652991SKI family transcriptional corepressor 2
INFERRED
HumanCBLN3643866cerebellin 3 precursor
INFERRED
HumanSUMF1285362sulfatase modifying factor 1
INFERRED
HumanPTF1A256297pancreas specific transcription factor, 1a
INFERRED
HumanSP8221833Sp8 transcription factor
INFERRED
HumanTBATA219793thymus, brain and testes associated
INFERRED
HumanPIKFYVE200576phosphoinositide kinase, FYVE finger containing
INFERRED
HumanDAB2IP153090DAB2 interacting protein
INFERRED
HumanEDARADD128178EDAR-associated death domain
Click here to display 214 evidence detail records.
HumanAK7122481adenylate kinase 7
Click here to display 214 evidence detail records.
HumanFOXP293986forkhead box P2
Click here to display 214 evidence detail records.
HumanCADPS293664Ca++-dependent secretion activator 2
Click here to display 214 evidence detail records.
HumanDNER92737delta/notch-like EGF repeat containing
INFERRED
HumanLMNB284823lamin B2
Click here to display 214 evidence detail records.
HumanPOMK84197protein-O-mannose kinase
Click here to display 214 evidence detail records.
HumanZIC484107Zic family member 4
INFERRED
HumanJAM383700junctional adhesion molecule 3
Click here to display 214 evidence detail records.
HumanCCM283605cerebral cavernous malformation 2
Click here to display 214 evidence detail records.
HumanPREX280243phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 2
INFERRED
HumanCEP29080184centrosomal protein 290kDa
Click here to display 214 evidence detail records.
HumanWLS79971wntless homolog (Drosophila)
INFERRED
HumanFA2H79152fatty acid 2-hydroxylase
Click here to display 214 evidence detail records.
HumanFKRP79147fukutin related protein
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000849abnormal cerebellum morphology0self