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Details
Link-It Detail - Jax Mouse Phenotype - abnormal hippocampus CA3 region morphology
Debug Stats
  • ### Total Build Time: 35 ms 19.410 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 412 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 192 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=4 ms Completed: 4 ms rowSize= 1.036 KB
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 586 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=5 ms Completed: 5 ms rowSize= 5.622 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=19 ms Completed: 19 ms rowSize= 10.266 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.180 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal hippocampus CA3 region morphology MP:0008267
Synonyms (1)
"abnormal CA3 field of Ammon's horn" EXACT
Parents (2)
img abnormal hippocampus region morphology MP:0008262
img abnormal Ammon gyrus morphology MP:0000815
Children (1)
img absent hippocampus CA3 region MP:0008268
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363111img abnormal hippocampus region morphology MP:0008262
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036319img abnormal hippocampus region morphology MP:0008262
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363111img abnormal Ammon gyrus morphology MP:0000815
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036319img abnormal Ammon gyrus morphology MP:0000815
Genes (17)

Species:
human : 17
SpeciesGeneGeneIdGene NameEvidence
HumanARX170302aristaless related homeobox
Click here to display 27 evidence detail records.
HumanFEZF255079FEZ family zinc finger 2
Click here to display 27 evidence detail records.
HumanPOMT229954protein-O-mannosyltransferase 2
Click here to display 27 evidence detail records.
HumanSS18L126039synovial sarcoma translocation gene on chromosome 18-like 1
Click here to display 27 evidence detail records.
HumanTP737161tumor protein p73
Click here to display 27 evidence detail records.
HumanSNAP256616synaptosomal-associated protein, 25kDa
Click here to display 27 evidence detail records.
HumanABCB15243ATP-binding cassette, sub-family B (MDR/TAP), member 1
Click here to display 27 evidence detail records.
HumanNPC14864Niemann-Pick disease, type C1
Click here to display 27 evidence detail records.
HumanNCAM14684neural cell adhesion molecule 1
Click here to display 27 evidence detail records.
HumanMAN2B14125mannosidase, alpha, class 2B, member 1
Click here to display 27 evidence detail records.
HumanLMX1A4009LIM homeobox transcription factor 1, alpha
Click here to display 27 evidence detail records.
HumanGRIA22891glutamate receptor, ionotropic, AMPA 2
Click here to display 27 evidence detail records.
HumanGPX42879glutathione peroxidase 4
Click here to display 27 evidence detail records.
HumanGDI12664GDP dissociation inhibitor 1
Click here to display 27 evidence detail records.
HumanDCX1641doublecortin
Click here to display 27 evidence detail records.
HumanCTNNB11499catenin (cadherin-associated protein), beta 1, 88kDa
INFERRED
HumanAGTR2186angiotensin II receptor, type 2
Click here to display 27 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0008267abnormal hippocampus CA3 region morphology0self