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Details
Link-It Detail - Jax Mouse Phenotype - abnormal cerebellum fissure morphology
Debug Stats
  • ### Total Build Time: 28 ms 67.855 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 404 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 297 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 196 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 592 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 582 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.583 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=24 ms Completed: 24 ms rowSize= 62.930 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.176 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal cerebellum fissure morphology MP:0009267
Definition (1)
any structural anomaly of the deep furrows which divide the lobules of the cerebellum, including the postcentral, primary and secondary furrows
Synonyms (1)
"abnormal cerebellar fissure morphology" EXACT
Parents (1)
img abnormal cerebellar cortex morphology MP:0004097
Children (1)
img absent cerebellum fissure MP:0009268
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036319img abnormal cerebellar cortex morphology MP:0004097
Genes (7)

Species:
human : 7
SpeciesGeneGeneIdGene NameEvidence
HumanEDARADD128178EDAR-associated death domain
img Jax MP, Pubmed Id: 22094718, MOUSE PHENOTYPE ID: MGI:3785283
img Jax MP, Pubmed Id: 23100420, MOUSE PHENOTYPE ID: MGI:104735
img Jax MP, Pubmed Id: 20980600, MOUSE PHENOTYPE ID: MGI:2176172
img Jax MP, Pubmed Id: 17344385, MOUSE PHENOTYPE ID: MGI:2443963
img Jax MP, Pubmed Id: 23074225, MOUSE PHENOTYPE ID: MGI:108090
img Jax MP, Pubmed Id: 20081196, MOUSE PHENOTYPE ID: MGI:104735
img Jax MP, Pubmed Id: 20081196, MOUSE PHENOTYPE ID: MGI:104735
img Jax MP, Pubmed Id: 21827743, MOUSE PHENOTYPE ID: MGI:1354695
img Jax MP, Pubmed Id: 21827743, MOUSE PHENOTYPE ID: MGI:1354695
img Jax MP, Pubmed Id: 22555591, MOUSE PHENOTYPE ID: MGI:95794
img Jax MP, Pubmed Id: 896803, MOUSE PHENOTYPE ID: MGI:1931001
img Jax MP, Pubmed Id: 20181585, MOUSE PHENOTYPE ID: MGI:1100537
img Jax MP, Pubmed Id: 10431235, MOUSE PHENOTYPE ID: MGI:1926792
HumanCADPS293664Ca++-dependent secretion activator 2
img Jax MP, Pubmed Id: 10431235, MOUSE PHENOTYPE ID: MGI:1926792
img Jax MP, Pubmed Id: 20980600, MOUSE PHENOTYPE ID: MGI:2176172
img Jax MP, Pubmed Id: 896803, MOUSE PHENOTYPE ID: MGI:1931001
img Jax MP, Pubmed Id: 23100420, MOUSE PHENOTYPE ID: MGI:104735
img Jax MP, Pubmed Id: 23074225, MOUSE PHENOTYPE ID: MGI:108090
img Jax MP, Pubmed Id: 21827743, MOUSE PHENOTYPE ID: MGI:1354695
img Jax MP, Pubmed Id: 20081196, MOUSE PHENOTYPE ID: MGI:104735
img Jax MP, Pubmed Id: 20081196, MOUSE PHENOTYPE ID: MGI:104735
img Jax MP, Pubmed Id: 22555591, MOUSE PHENOTYPE ID: MGI:95794
img Jax MP, Pubmed Id: 17344385, MOUSE PHENOTYPE ID: MGI:2443963
img Jax MP, Pubmed Id: 22094718, MOUSE PHENOTYPE ID: MGI:3785283
img Jax MP, Pubmed Id: 21827743, MOUSE PHENOTYPE ID: MGI:1354695
img Jax MP, Pubmed Id: 20181585, MOUSE PHENOTYPE ID: MGI:1100537
HumanRIC8A60626RIC8 guanine nucleotide exchange factor A
INFERRED
HumanFBXW755294F-box and WD repeat domain containing 7, E3 ubiquitin protein ligase
img Jax MP, Pubmed Id: 22555591, MOUSE PHENOTYPE ID: MGI:95794
img Jax MP, Pubmed Id: 17344385, MOUSE PHENOTYPE ID: MGI:2443963
img Jax MP, Pubmed Id: 21827743, MOUSE PHENOTYPE ID: MGI:1354695
img Jax MP, Pubmed Id: 20081196, MOUSE PHENOTYPE ID: MGI:104735
img Jax MP, Pubmed Id: 23074225, MOUSE PHENOTYPE ID: MGI:108090
img Jax MP, Pubmed Id: 896803, MOUSE PHENOTYPE ID: MGI:1931001
img Jax MP, Pubmed Id: 23100420, MOUSE PHENOTYPE ID: MGI:104735
img Jax MP, Pubmed Id: 20081196, MOUSE PHENOTYPE ID: MGI:104735
img Jax MP, Pubmed Id: 10431235, MOUSE PHENOTYPE ID: MGI:1926792
img Jax MP, Pubmed Id: 21827743, MOUSE PHENOTYPE ID: MGI:1354695
img Jax MP, Pubmed Id: 20181585, MOUSE PHENOTYPE ID: MGI:1100537
img Jax MP, Pubmed Id: 22094718, MOUSE PHENOTYPE ID: MGI:3785283
img Jax MP, Pubmed Id: 20980600, MOUSE PHENOTYPE ID: MGI:2176172
HumanEI249538etoposide induced 2.4
img Jax MP, Pubmed Id: 20181585, MOUSE PHENOTYPE ID: MGI:1100537
img Jax MP, Pubmed Id: 20081196, MOUSE PHENOTYPE ID: MGI:104735
img Jax MP, Pubmed Id: 22555591, MOUSE PHENOTYPE ID: MGI:95794
img Jax MP, Pubmed Id: 22094718, MOUSE PHENOTYPE ID: MGI:3785283
img Jax MP, Pubmed Id: 20980600, MOUSE PHENOTYPE ID: MGI:2176172
img Jax MP, Pubmed Id: 17344385, MOUSE PHENOTYPE ID: MGI:2443963
img Jax MP, Pubmed Id: 20081196, MOUSE PHENOTYPE ID: MGI:104735
img Jax MP, Pubmed Id: 21827743, MOUSE PHENOTYPE ID: MGI:1354695
img Jax MP, Pubmed Id: 23100420, MOUSE PHENOTYPE ID: MGI:104735
img Jax MP, Pubmed Id: 21827743, MOUSE PHENOTYPE ID: MGI:1354695
img Jax MP, Pubmed Id: 896803, MOUSE PHENOTYPE ID: MGI:1931001
img Jax MP, Pubmed Id: 23074225, MOUSE PHENOTYPE ID: MGI:108090
img Jax MP, Pubmed Id: 10431235, MOUSE PHENOTYPE ID: MGI:1926792
HumanMID14281midline 1 (Opitz/BBB syndrome)
img Jax MP, Pubmed Id: 21827743, MOUSE PHENOTYPE ID: MGI:1354695
img Jax MP, Pubmed Id: 10431235, MOUSE PHENOTYPE ID: MGI:1926792
img Jax MP, Pubmed Id: 17344385, MOUSE PHENOTYPE ID: MGI:2443963
img Jax MP, Pubmed Id: 20081196, MOUSE PHENOTYPE ID: MGI:104735
img Jax MP, Pubmed Id: 21827743, MOUSE PHENOTYPE ID: MGI:1354695
img Jax MP, Pubmed Id: 20980600, MOUSE PHENOTYPE ID: MGI:2176172
img Jax MP, Pubmed Id: 22555591, MOUSE PHENOTYPE ID: MGI:95794
img Jax MP, Pubmed Id: 20181585, MOUSE PHENOTYPE ID: MGI:1100537
img Jax MP, Pubmed Id: 23074225, MOUSE PHENOTYPE ID: MGI:108090
img Jax MP, Pubmed Id: 22094718, MOUSE PHENOTYPE ID: MGI:3785283
img Jax MP, Pubmed Id: 23100420, MOUSE PHENOTYPE ID: MGI:104735
img Jax MP, Pubmed Id: 896803, MOUSE PHENOTYPE ID: MGI:1931001
img Jax MP, Pubmed Id: 20081196, MOUSE PHENOTYPE ID: MGI:104735
HumanLRP24036low density lipoprotein receptor-related protein 2
img Jax MP, Pubmed Id: 21827743, MOUSE PHENOTYPE ID: MGI:1354695
img Jax MP, Pubmed Id: 23074225, MOUSE PHENOTYPE ID: MGI:108090
img Jax MP, Pubmed Id: 20181585, MOUSE PHENOTYPE ID: MGI:1100537
img Jax MP, Pubmed Id: 20980600, MOUSE PHENOTYPE ID: MGI:2176172
img Jax MP, Pubmed Id: 22094718, MOUSE PHENOTYPE ID: MGI:3785283
img Jax MP, Pubmed Id: 22555591, MOUSE PHENOTYPE ID: MGI:95794
img Jax MP, Pubmed Id: 10431235, MOUSE PHENOTYPE ID: MGI:1926792
img Jax MP, Pubmed Id: 20081196, MOUSE PHENOTYPE ID: MGI:104735
img Jax MP, Pubmed Id: 23100420, MOUSE PHENOTYPE ID: MGI:104735
img Jax MP, Pubmed Id: 21827743, MOUSE PHENOTYPE ID: MGI:1354695
img Jax MP, Pubmed Id: 896803, MOUSE PHENOTYPE ID: MGI:1931001
img Jax MP, Pubmed Id: 17344385, MOUSE PHENOTYPE ID: MGI:2443963
img Jax MP, Pubmed Id: 20081196, MOUSE PHENOTYPE ID: MGI:104735
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0009267abnormal cerebellum fissure morphology0self