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Details
Link-It Detail - Jax Mouse Phenotype - abnormal cerebellum vermis morphology
Debug Stats
  • ### Total Build Time: 236 ms 23.091 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 402 bytes
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  • CONCEPT_GENES gt=117 ms Completed: 117 ms rowSize= 15.910 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.175 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal cerebellum vermis morphology MP:0000864
Definition (1)
any structural anomaly of the narrow medial zone between the two hemispheres of the cerebellum that is delimited by two longitudinal furrows; it may be continuous with the cerebellar hemispheres in some areas of the cerebellum, e.g., dorsally, or separated by deeper fissues in others (e.g., ventrally); it receives inputs from the spinocerebellar tracts which carry to the vermis information on the position and balance of the torso, and it sends projections to the fastigial nucleus of the cerebellum, which then sends output to the vestibular nuclei
Synonyms (1)
"cerebellum vermis dysplasia" EXACT
Parents (1)
img abnormal cerebellar cortex morphology MP:0004097
Children (5)
img abnormal cerebellum posterior vermis morphology MP:0000869
img abnormal cerebellum vermis lobule morphology MP:0009957
img absent cerebellum vermis MP:0000865
img cerebellum vermis hypoplasia MP:0000866
img abnormal cerebellum anterior vermis morphology MP:0000867
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036319img abnormal cerebellar cortex morphology MP:0004097
Genes (37)

Species:
human : 37
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanZIC484107Zic family member 4
Click here to display 38 evidence detail records.
HumanCEP29080184centrosomal protein 290kDa
Click here to display 38 evidence detail records.
HumanEBF264641early B-cell factor 2
INFERRED
HumanSCYL157410SCY1-like 1 (S. cerevisiae)
Click here to display 38 evidence detail records.
HumanPDSS257107prenyl (decaprenyl) diphosphate synthase, subunit 2
INFERRED
HumanFBXW755294F-box and WD repeat domain containing 7, E3 ubiquitin protein ligase
INFERRED
HumanMKS154903Meckel syndrome, type 1
INFERRED
HumanAHI154806Abelson helper integration site 1
Click here to display 38 evidence detail records.
HumanFOXB127023forkhead box B1
INFERRED
HumanZNF42323090zinc finger protein 423
Click here to display 38 evidence detail records.
HumanCERS110715ceramide synthase 1
INFERRED
HumanCACNA2D29254calcium channel, voltage-dependent, alpha 2/delta subunit 2
INFERRED
HumanFGF178822fibroblast growth factor 17
Click here to display 38 evidence detail records.
HumanNAPA8775N-ethylmaleimide-sensitive factor attachment protein, alpha
Click here to display 38 evidence detail records.
HumanNUMB8650numb homolog (Drosophila)
Click here to display 38 evidence detail records.
HumanUNC5C8633unc-5 homolog C (C. elegans)
INFERRED
HumanZIC17545Zic family member 1
Click here to display 38 evidence detail records.
HumanXRCC47518X-ray repair complementing defective repair in Chinese hamster cells 4
Click here to display 38 evidence detail records.
HumanATXN76314ataxin 7
Click here to display 38 evidence detail records.
HumanRBL15933retinoblastoma-like 1 (p107)
Click here to display 38 evidence detail records.
HumanPTEN5728phosphatase and tensin homolog
Click here to display 38 evidence detail records.
HumanPAX65080paired box 6
Click here to display 38 evidence detail records.
HumanPAX55079paired box 5
Click here to display 38 evidence detail records.
HumanNPC14864Niemann-Pick disease, type C1
INFERRED
HumanMSX24488msh homeobox 2
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000864abnormal cerebellum vermis morphology0self