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Details
Link-It Detail - Jax Mouse Phenotype - absent hippocampal commissure
Debug Stats
  • ### Total Build Time: 35 ms 14.384 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 386 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 413 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 169 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=2 ms Completed: 2 ms rowSize= 597 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=9 ms Completed: 9 ms rowSize= 2.941 KB
  • CONCEPT_RELATIONSHIPS gt=2 ms Completed: 2 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=17 ms Completed: 17 ms rowSize= 8.595 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.167 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
absent hippocampal commissure MP:0008223
Definition (1)
absence of the triangular subcallosal plate of commissural fibers resulting from the converging of the right and left fornix bundles which exchange numerous fibers and which curve back in the contralateral fornix to end in the hippocampus of the opposite side
Synonyms (1)
"absent vhc" NARROW
Parents (1)
img abnormal hippocampal commissure morphology MP:0008221
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036319img abnormal hippocampal commissure morphology MP:0008221
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036318img abnormal hippocampal commissure morphology MP:0008221
Genes (14)

Species:
human : 14
SpeciesGeneGeneIdGene NameEvidence
HumanDRAXIN374946dorsal inhibitory axon guidance protein
Click here to display 19 evidence detail records.
HumanARX170302aristaless related homeobox
Click here to display 19 evidence detail records.
HumanLHX564211LIM homeobox 5
Click here to display 19 evidence detail records.
HumanPRDM856978PR domain containing 8
Click here to display 19 evidence detail records.
HumanBHLHE2227319basic helix-loop-helix family, member e22
Click here to display 19 evidence detail records.
HumanVTI1B10490vesicle transport through interaction with t-SNAREs 1B
Click here to display 19 evidence detail records.
HumanNTN19423netrin 1
Click here to display 19 evidence detail records.
HumanDCLK19201doublecortin-like kinase 1
Click here to display 19 evidence detail records.
HumanMAP1B4131microtubule-associated protein 1B
Click here to display 19 evidence detail records.
HumanARHGAP352909Rho GTPase activating protein 35
Click here to display 19 evidence detail records.
HumanGLI32737GLI family zinc finger 3
Click here to display 19 evidence detail records.
HumanDCX1641doublecortin
Click here to display 19 evidence detail records.
HumanDCC1630deleted in colorectal carcinoma
Click here to display 19 evidence detail records.
HumanCTNNB11499catenin (cadherin-associated protein), beta 1, 88kDa
Click here to display 19 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0008223absent hippocampal commissure0self