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Details
Link-It Detail - Jax Mouse Phenotype - abnormal cerebral aqueduct morphology
Debug Stats
  • ### Total Build Time: 82 ms 15.309 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 402 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 258 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 186 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=12 ms Completed: 12 ms rowSize= 583 bytes
  • CONCEPT_CHILDREN gt=10 ms Completed: 10 ms rowSize= 576 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=11 ms Completed: 11 ms rowSize= 2.914 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=38 ms Completed: 38 ms rowSize= 9.117 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.175 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal cerebral aqueduct morphology MP:0005537
Definition (1)
any structural anomaly of the channel in the mesencephalon that connects the third and fourth ventricles
Synonyms (1)
"abnormal aqueduct of Sylvius" EXACT
Parents (1)
img abnormal midbrain morphology MP:0000897
Children (1)
img aqueductal stenosis MP:0002958
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036317img abnormal midbrain morphology MP:0000897
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036316img abnormal midbrain morphology MP:0000897
Genes (15)

Species:
human : 15
SpeciesGeneGeneIdGene NameEvidence
HumanKDM2B84678lysine (K)-specific demethylase 2B
Click here to display 21 evidence detail records.
HumanNPAS364067neuronal PAS domain protein 3
Click here to display 21 evidence detail records.
HumanMKS154903Meckel syndrome, type 1
Click here to display 21 evidence detail records.
HumanDPCD25911deleted in primary ciliary dyskinesia homolog (mouse)
Click here to display 21 evidence detail records.
HumanNR1H310062nuclear receptor subfamily 1, group H, member 3
Click here to display 21 evidence detail records.
HumanDLG59231discs, large homolog 5 (Drosophila)
Click here to display 21 evidence detail records.
HumanNAPA8775N-ethylmaleimide-sensitive factor attachment protein, alpha
Click here to display 21 evidence detail records.
HumanRFX45992regulatory factor X, 4 (influences HLA class II expression)
INFERRED
HumanOTX15013orthodenticle homeobox 1
Click here to display 21 evidence detail records.
HumanNEK14750NIMA-related kinase 1
Click here to display 21 evidence detail records.
HumanL1CAM3897L1 cell adhesion molecule
Click here to display 21 evidence detail records.
HumanHTT3064huntingtin
Click here to display 21 evidence detail records.
HumanGLI32737GLI family zinc finger 3
Click here to display 21 evidence detail records.
HumanERBB32065v-erb-b2 avian erythroblastic leukemia viral oncogene homolog 3
Click here to display 21 evidence detail records.
HumanCDC42998cell division cycle 42
Click here to display 21 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0005537abnormal cerebral aqueduct morphology0self