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Details
Link-It Detail - Jax Mouse Phenotype - abnormal palatal shelf fusion at midline
Debug Stats
  • ### Total Build Time: 48 ms 26.827 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 408 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 346 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=4 ms Completed: 4 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= 1.026 KB
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.072 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 6.958 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=34 ms Completed: 34 ms rowSize= 15.712 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.178 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal palatal shelf fusion at midline MP:0009887
Definition (1)
any anomaly in the process in which the palatal shelves grow toward the midline and adhere along the medial edge epithelia, forming the midline epithelial seam which disappears in later stages
Parents (2)
img cleft secondary palate MP:0009890
img abnormal secondary palate development MP:0009655
Children (2)
img palatal shelves fail to meet at midline MP:0009888
img persistence of medial edge epithelium during palatal shelf fusion MP:0009889
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img digestive/alimentary phenotype MP:00053817img cleft secondary palate MP:0009890
img mammalian phenotype MP:0000001img craniofacial phenotype MP:000538211img cleft secondary palate MP:0009890
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053827img abnormal secondary palate development MP:0009655
img mammalian phenotype MP:0000001img digestive/alimentary phenotype MP:00053817img abnormal secondary palate development MP:0009655
img mammalian phenotype MP:0000001img craniofacial phenotype MP:000538211img abnormal secondary palate development MP:0009655
Genes (61)

Species:
human : 61
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanLHX8431707LIM homeobox 8
INFERRED
HumanRSPO2340419R-spondin 2
Click here to display 31 evidence detail records.
HumanOSR2116039odd-skipped related 2 (Drosophila)
INFERRED
HumanWDR1957728WD repeat domain 19
Click here to display 31 evidence detail records.
HumanINPP5E56623inositol polyphosphate-5-phosphatase, 72 kDa
INFERRED
HumanPDGFC56034platelet derived growth factor C
Click here to display 31 evidence detail records.
HumanBNC254796basonuclin 2
INFERRED
HumanSCHIP129970schwannomin interacting protein 1
Click here to display 31 evidence detail records.
HumanSATB223314SATB homeobox 2
INFERRED
HumanPDS5A23244PDS5, regulator of cohesion maintenance, homolog A (S. cerevisiae)
INFERRED
HumanNCOA623054nuclear receptor coactivator 6
Click here to display 31 evidence detail records.
HumanPDS5B23047PDS5, regulator of cohesion maintenance, homolog B (S. cerevisiae)
Click here to display 31 evidence detail records.
HumanTSHZ110194teashirt zinc finger homeobox 1
Click here to display 31 evidence detail records.
HumanNCOR29612nuclear receptor corepressor 2
INFERRED
HumanHAND29464heart and neural crest derivatives expressed 2
Click here to display 31 evidence detail records.
HumanSGPL18879sphingosine-1-phosphate lyase 1
Click here to display 31 evidence detail records.
HumanCHRD8646chordin
INFERRED
HumanCASK8573calcium/calmodulin-dependent serine protein kinase (MAGUK family)
INFERRED
HumanFZD18321frizzled family receptor 1
INFERRED
HumanLUZP17798leucine zipper protein 1
INFERRED
HumanTGFB37043transforming growth factor, beta 3
INFERRED
HumanTGFB17040transforming growth factor, beta 1
Click here to display 31 evidence detail records.
HumanTFAP2A7020transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
Click here to display 31 evidence detail records.
HumanTCOF16949Treacher Collins-Franceschetti syndrome 1
Click here to display 31 evidence detail records.
HumanZEB16935zinc finger E-box binding homeobox 1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0009887abnormal palatal shelf fusion at midline0self