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Details
Link-It Detail - Jax Mouse Phenotype - abnormal secondary palate development
Debug Stats
  • ### Total Build Time: 212 ms 24.106 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 402 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 395 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=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=32 ms Completed: 32 ms rowSize= 582 bytes
  • CONCEPT_CHILDREN gt=49 ms Completed: 49 ms rowSize= 2.409 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=39 ms Completed: 39 ms rowSize= 4.255 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=82 ms Completed: 82 ms rowSize= 14.776 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.175 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal secondary palate development MP:0009655
Definition (1)
any anomaly in the formation of the part of the palate that is formed during embryonic development when palatal projections from the inner part of the maxillary processes emerge, extend and elevate into a horizontal position above the tongue
Parents (1)
img abnormal palate development MP:0009653
Children (5)
img abnormal palatal shelf fusion at midline MP:0009887
img palatal shelf hypoplasia MP:0009883
img absent palatal shelf MP:0009882
img palatal shelf fusion with tongue or mandible MP:0009884
img abnormal palatal shelf elevation MP:0009885
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053826img abnormal palate development MP:0009653
img mammalian phenotype MP:0000001img digestive/alimentary phenotype MP:00053816img abnormal palate development MP:0009653
img mammalian phenotype MP:0000001img craniofacial phenotype MP:000538210img abnormal palate development MP:0009653
Genes (94)

Species:
human : 94
Page Size
Current 25
  Page 1 of 4
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanLHX8431707LIM homeobox 8
INFERRED
HumanTBX10347853T-box 10
INFERRED
HumanRSPO2340419R-spondin 2
INFERRED
HumanSLC32A1140679solute carrier family 32 (GABA vesicular transporter), member 1
INFERRED
HumanOSR2116039odd-skipped related 2 (Drosophila)
INFERRED
HumanPKDCC91461protein kinase domain containing, cytoplasmic
INFERRED
HumanTMEM10784314transmembrane protein 107
INFERRED
HumanFUZ80199fuzzy planar cell polarity protein
INFERRED
HumanPRDM1663976PR domain containing 16
INFERRED
HumanWDR1957728WD repeat domain 19
INFERRED
HumanINPP5E56623inositol polyphosphate-5-phosphatase, 72 kDa
INFERRED
HumanPDGFC56034platelet derived growth factor C
INFERRED
HumanHHAT55733hedgehog acyltransferase
INFERRED
HumanCHD755636chromodomain helicase DNA binding protein 7
Click here to display 24 evidence detail records.
HumanBNC254796basonuclin 2
INFERRED
HumanCDON50937cell adhesion associated, oncogene regulated
Click here to display 24 evidence detail records.
HumanSCHIP129970schwannomin interacting protein 1
INFERRED
HumanSATB223314SATB homeobox 2
INFERRED
HumanPDS5A23244PDS5, regulator of cohesion maintenance, homolog A (S. cerevisiae)
INFERRED
HumanNCOA623054nuclear receptor coactivator 6
INFERRED
HumanPDS5B23047PDS5, regulator of cohesion maintenance, homolog B (S. cerevisiae)
INFERRED
HumanTSHZ110194teashirt zinc finger homeobox 1
INFERRED
HumanNCOR29612nuclear receptor corepressor 2
INFERRED
HumanHAND29464heart and neural crest derivatives expressed 2
Click here to display 24 evidence detail records.
HumanSGPL18879sphingosine-1-phosphate lyase 1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0009655abnormal secondary palate development0self