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Details
Link-It Detail - Jax Mouse Phenotype - abnormal ameloblast morphology
Debug Stats
  • ### Total Build Time: 43 ms 15.567 KB
  • CONCEPT_NAME gt=2 ms Completed: 1 ms rowSize= 388 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 263 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 193 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=5 ms Completed: 5 ms rowSize= 581 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 580 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 2.907 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=27 ms Completed: 27 ms rowSize= 9.390 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.168 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal ameloblast morphology MP:0002650
Definition (1)
any structural anomaly of the epithelial cells of the inner layer of the enamel organ of the developing tooth
Synonyms (1)
"abnormal ameloblast cell morphology" EXACT
Parents (1)
img abnormal tooth development MP:0000116
Children (1)
img ameloblast degeneration MP:0000129
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img craniofacial phenotype MP:000538210img abnormal tooth development MP:0000116
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053826img abnormal tooth development MP:0000116
Genes (16)

Species:
human : 16
SpeciesGeneGeneIdGene NameEvidence
HumanSP680320Sp6 transcription factor
Click here to display 25 evidence detail records.
HumanBCL11B64919B-cell CLL/lymphoma 11B (zinc finger protein)
Click here to display 25 evidence detail records.
HumanFAM20A54757family with sequence similarity 20, member A
Click here to display 25 evidence detail records.
HumanPOSTN10631periostin, osteoblast specific factor
Click here to display 25 evidence detail records.
HumanAGPAT2105551-acylglycerol-3-phosphate O-acyltransferase 2
INFERRED
HumanMMP209313matrix metallopeptidase 20
Click here to display 25 evidence detail records.
HumanSP36670Sp3 transcription factor
Click here to display 25 evidence detail records.
HumanSMO6608smoothened, frizzled family receptor
Click here to display 25 evidence detail records.
HumanPVRL15818poliovirus receptor-related 1 (herpesvirus entry mediator C)
Click here to display 25 evidence detail records.
HumanPRRX15396paired related homeobox 1
Click here to display 25 evidence detail records.
HumanPAX95083paired box 9
Click here to display 25 evidence detail records.
HumanNFE2L24780nuclear factor, erythroid 2-like 2
INFERRED
HumanMSX24488msh homeobox 2
INFERRED
HumanLAMA33909laminin, alpha 3
Click here to display 25 evidence detail records.
HumanAMELX265amelogenin, X-linked
Click here to display 25 evidence detail records.
HumanAMBN258ameloblastin (enamel matrix protein)
Click here to display 25 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002650abnormal ameloblast morphology0self