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Details
Link-It Detail - Jax Mouse Phenotype - midline facial cleft
Debug Stats
  • ### Total Build Time: 38 ms 15.732 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 368 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 293 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=5 ms Completed: 5 ms rowSize= 567 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 1.557 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=28 ms Completed: 28 ms rowSize= 11.666 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.158 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
midline facial cleft MP:0000108
Definition (1)
incomplete merging or fusion of the tissues (e.g. the two globular processes) along the facial midline that normally unite to form the face
Parents (1)
img facial cleft MP:0008797
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053827img facial cleft MP:0008797
Genes (19)

Species:
human : 19
SpeciesGeneGeneIdGene NameEvidence
HumanRDH10157506retinol dehydrogenase 10 (all-trans)
Click here to display 38 evidence detail records.
HumanFBXO1180204F-box protein 11
Click here to display 38 evidence detail records.
HumanALX460529ALX homeobox 4
Click here to display 38 evidence detail records.
HumanPLEKHA159338pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1
Click here to display 38 evidence detail records.
HumanSHROOM357619shroom family member 3
Click here to display 38 evidence detail records.
HumanPDGFC56034platelet derived growth factor C
Click here to display 38 evidence detail records.
HumanCECR227443cat eye syndrome chromosome region, candidate 2
Click here to display 38 evidence detail records.
HumanFOXD327022forkhead box D3
Click here to display 38 evidence detail records.
HumanTACC310460transforming, acidic coiled-coil containing protein 3
Click here to display 38 evidence detail records.
HumanGTF2IRD19569GTF2I repeat domain containing 1
Click here to display 38 evidence detail records.
HumanALX18092ALX homeobox 1
Click here to display 38 evidence detail records.
HumanTFAP2A7020transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
Click here to display 38 evidence detail records.
HumanZEB16935zinc finger E-box binding homeobox 1
Click here to display 38 evidence detail records.
HumanSKI6497v-ski avian sarcoma viral oncogene homolog
Click here to display 38 evidence detail records.
HumanPDGFRA5156platelet-derived growth factor receptor, alpha polypeptide
Click here to display 38 evidence detail records.
HumanGTF2I2969general transcription factor IIi
Click here to display 38 evidence detail records.
HumanELAVL11994ELAV (embryonic lethal, abnormal vision, Drosophila)-like 1 (Hu antigen R)
Click here to display 38 evidence detail records.
HumanAPAF1317apoptotic peptidase activating factor 1
Click here to display 38 evidence detail records.
HumanALX3257ALX homeobox 3
Click here to display 38 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000108midline facial cleft0self