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Details
Link-It Detail - Jax Mouse Phenotype - abnormal squamosal bone morphology
Debug Stats
  • ### Total Build Time: 108 ms 19.405 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 396 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 226 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=8 ms Completed: 8 ms rowSize= 588 bytes
  • CONCEPT_CHILDREN gt=9 ms Completed: 8 ms rowSize= 1.011 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=6 ms Completed: 6 ms rowSize= 2.916 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=78 ms Completed: 78 ms rowSize= 12.980 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.172 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal squamosal bone morphology MP:0004423
Definition (1)
any structural anomaly of the thin, plate-like part of the temporal bone
Parents (1)
img abnormal temporal bone morphology MP:0005272
Children (2)
img short squamosal bone MP:0008430
img absent squamosal bone MP:0004899
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053828img abnormal temporal bone morphology MP:0005272
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053909img abnormal temporal bone morphology MP:0005272
Genes (23)

Species:
human : 23
SpeciesGeneGeneIdGene NameEvidence
HumanRSPO2340419R-spondin 2
Click here to display 37 evidence detail records.
HumanBMPER168667BMP binding endothelial regulator
Click here to display 37 evidence detail records.
HumanSCUBE180274signal peptide, CUB domain, EGF-like 1
Click here to display 37 evidence detail records.
HumanALX460529ALX homeobox 4
INFERRED
HumanCHRD8646chordin
Click here to display 37 evidence detail records.
HumanALX18092ALX homeobox 1
Click here to display 37 evidence detail records.
HumanWNT17471wingless-type MMTV integration site family, member 1
Click here to display 37 evidence detail records.
HumanTWIST17291twist basic helix-loop-helix transcription factor 1
INFERRED
HumanSMO6608smoothened, frizzled family receptor
Click here to display 37 evidence detail records.
HumanSIX16495SIX homeobox 1
INFERRED
HumanRARA5914retinoic acid receptor, alpha
Click here to display 37 evidence detail records.
HumanPOU3F35455POU class 3 homeobox 3
INFERRED
HumanPRRX15396paired related homeobox 1
INFERRED
HumanMN14330meningioma (disrupted in balanced translocation) 1
INFERRED
HumanHOXA23199homeobox A2
Click here to display 37 evidence detail records.
HumanHMX13166H6 family homeobox 1
Click here to display 37 evidence detail records.
HumanFOXC22303forkhead box C2 (MFH-1, mesenchyme forkhead 1)
Click here to display 37 evidence detail records.
HumanFGFR12260fibroblast growth factor receptor 1
Click here to display 37 evidence detail records.
HumanEDNRA1909endothelin receptor type A
Click here to display 37 evidence detail records.
HumanECE11889endothelin converting enzyme 1
Click here to display 37 evidence detail records.
HumanDLX61750distal-less homeobox 6
Click here to display 37 evidence detail records.
HumanDLX51749distal-less homeobox 5
Click here to display 37 evidence detail records.
HumanBMP7655bone morphogenetic protein 7
Click here to display 37 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004423abnormal squamosal bone morphology0self