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Details
Link-It Detail - Jax Mouse Phenotype - absent cerebellum fissure
Debug Stats
  • ### Total Build Time: 33 ms 7.130 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 378 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 282 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 183 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=8 ms Completed: 8 ms rowSize= 593 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=6 ms Completed: 6 ms rowSize= 1.585 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 2.827 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.163 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
absent cerebellum fissure MP:0009268
Definition (1)
absence of the deep furrows which divide the lobules of the cerebellum, including the postcentral, primary and secondary furrows
Synonyms (1)
"absent cerebellar fissure" EXACT
Parents (1)
img abnormal cerebellum fissure morphology MP:0009267
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363110img abnormal cerebellum fissure morphology MP:0009267
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanRIC8A60626RIC8 guanine nucleotide exchange factor A
img Jax MP, Pubmed Id: 23100420, MOUSE PHENOTYPE ID: MGI:2141866
img Jax MP, Pubmed Id: 20980600, MOUSE PHENOTYPE ID: MGI:2176172
img Jax MP
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0009268absent cerebellum fissure0self