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Details
Link-It Detail - Jax Mouse Phenotype - facial cleft
Debug Stats
  • ### Total Build Time: 135 ms 20.812 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 352 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 283 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 181 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=55 ms Completed: 55 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= 581 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.457 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=7 ms Completed: 7 ms rowSize= 1.570 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=54 ms Completed: 54 ms rowSize= 15.125 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.150 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
facial cleft MP:0008797
Definition (1)
a cleft resulting from incomplete merging or fusion of any of the embryonic facial processes that normally unite to form the face
Synonyms (1)
"split-face malformation" EXACT
Parents (1)
img abnormal facial morphology MP:0003743
Children (3)
img lateral facial cleft MP:0008798
img oblique facial cleft MP:0008799
img midline facial cleft MP:0000108
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053826img abnormal facial morphology MP:0003743
Genes (28)

Species:
human : 28
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanRDH10157506retinol dehydrogenase 10 (all-trans)
Click here to display 27 evidence detail records.
HumanTRIM71131405tripartite motif containing 71, E3 ubiquitin protein ligase
Click here to display 27 evidence detail records.
HumanNUAK281788NUAK family, SNF1-like kinase, 2
Click here to display 27 evidence detail records.
HumanFBXO1180204F-box protein 11
INFERRED
HumanGRHL279977grainyhead-like 2 (Drosophila)
Click here to display 27 evidence detail records.
HumanALX460529ALX homeobox 4
INFERRED
HumanPLEKHA159338pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1
INFERRED
HumanSHROOM357619shroom family member 3
INFERRED
HumanPDGFC56034platelet derived growth factor C
INFERRED
HumanCECR227443cat eye syndrome chromosome region, candidate 2
INFERRED
HumanFOXD327022forkhead box D3
INFERRED
HumanTACC310460transforming, acidic coiled-coil containing protein 3
INFERRED
HumanGTF2IRD19569GTF2I repeat domain containing 1
INFERRED
HumanALX18092ALX homeobox 1
INFERRED
HumanSUMO17341small ubiquitin-like modifier 1
INFERRED
HumanTULP37289tubby like protein 3
Click here to display 27 evidence detail records.
HumanTFAP2A7020transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
INFERRED
HumanZEB16935zinc finger E-box binding homeobox 1
INFERRED
HumanSKI6497v-ski avian sarcoma viral oncogene homolog
INFERRED
HumanPDGFRA5156platelet-derived growth factor receptor, alpha polypeptide
INFERRED
HumanNDST13340N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1
Click here to display 27 evidence detail records.
HumanGTF2I2969general transcription factor IIi
INFERRED
HumanFGFR12260fibroblast growth factor receptor 1
Click here to display 27 evidence detail records.
HumanELAVL11994ELAV (embryonic lethal, abnormal vision, Drosophila)-like 1 (Hu antigen R)
INFERRED
HumanEDNRA1909endothelin receptor type A
Click here to display 27 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0008797facial cleft0self