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Details
Link-It Detail - Jax Mouse Phenotype - abnormal Meckel's cartilage morphology
Debug Stats
  • ### Total Build Time: 61 ms 23.807 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 404 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 377 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 194 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=4 ms Completed: 4 ms rowSize= 1.029 KB
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 582 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.912 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=51 ms Completed: 51 ms rowSize= 17.024 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.176 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal Meckel's cartilage morphology MP:0005587
Definition (1)
any structural anomaly of this cartilage bar in the mandibular arch that forms a temporary supporting structure in the embryonic mandible; gives rise to middle ear bones and sphenomandibular and anterior malleolar ligaments
Synonyms (1)
"abnormal Meckel cartilage morphology" EXACT
Parents (2)
img abnormal cartilage morphology MP:0000163
img abnormal craniofacial development MP:0003935
Children (1)
img absent Meckel's cartilage MP:0004439
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053905img abnormal cartilage morphology MP:0000163
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053825img abnormal craniofacial development MP:0003935
Genes (34)

Species:
human : 34
Page Size
Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanRSPO2340419R-spondin 2
Click here to display 49 evidence detail records.
HumanGSC145258goosecoid homeobox
Click here to display 49 evidence detail records.
HumanFUZ80199fuzzy planar cell polarity protein
Click here to display 49 evidence detail records.
HumanPRDM1663976PR domain containing 16
Click here to display 49 evidence detail records.
HumanFLVCR128982feline leukemia virus subgroup C cellular receptor 1
Click here to display 49 evidence detail records.
HumanHAND29464heart and neural crest derivatives expressed 2
Click here to display 49 evidence detail records.
HumanZEB16935zinc finger E-box binding homeobox 1
Click here to display 49 evidence detail records.
HumanSOX96662SRY (sex determining region Y)-box 9
Click here to display 49 evidence detail records.
HumanSMO6608smoothened, frizzled family receptor
Click here to display 49 evidence detail records.
HumanSNAI26591snail family zinc finger 2
Click here to display 49 evidence detail records.
HumanSIX16495SIX homeobox 1
Click here to display 49 evidence detail records.
HumanPRRX15396paired related homeobox 1
Click here to display 49 evidence detail records.
HumanPKD15310polycystic kidney disease 1 (autosomal dominant)
Click here to display 49 evidence detail records.
HumanPITX25308paired-like homeodomain 2
Click here to display 49 evidence detail records.
HumanPITX15307paired-like homeodomain 1
Click here to display 49 evidence detail records.
HumanOTX25015orthodenticle homeobox 2
Click here to display 49 evidence detail records.
HumanROR24920receptor tyrosine kinase-like orphan receptor 2
Click here to display 49 evidence detail records.
HumanMSX14487msh homeobox 1
Click here to display 49 evidence detail records.
HumanMMP144323matrix metallopeptidase 14 (membrane-inserted)
Click here to display 49 evidence detail records.
HumanSMAD24087SMAD family member 2
Click here to display 49 evidence detail records.
HumanLRP64040low density lipoprotein receptor-related protein 6
Click here to display 49 evidence detail records.
HumanHOXA23199homeobox A2
Click here to display 49 evidence detail records.
HumanFOXC22303forkhead box C2 (MFH-1, mesenchyme forkhead 1)
Click here to display 49 evidence detail records.
HumanFGF92254fibroblast growth factor 9
Click here to display 49 evidence detail records.
HumanEGFR1956epidermal growth factor receptor
Click here to display 49 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0005587abnormal Meckel's cartilage morphology0self