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Details
Link-It Detail - Jax Mouse Phenotype - abnormal alisphenoid bone morphology
Debug Stats
  • ### Total Build Time: 86 ms 18.755 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 400 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 307 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 198 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=6 ms Completed: 6 ms rowSize= 588 bytes
  • CONCEPT_CHILDREN gt=7 ms Completed: 7 ms rowSize= 1.015 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=5 ms Completed: 5 ms rowSize= 2.916 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=51 ms Completed: 51 ms rowSize= 12.048 KB
  • CONCEPT_XREFS gt=7 ms Completed: 7 ms rowSize= 1.174 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal alisphenoid bone morphology MP:0003235
Definition (1)
any structural anomaly of either of the broad curved wing like expanses on each side of the sphenoid bone in adults; may exist independently in the young
Synonyms (1)
"abnormal great wing of the sphenoid bone" EXACT
Parents (1)
img abnormal sphenoid bone morphology MP:0000104
Children (2)
img small alisphenoid bone MP:0004459
img absent alisphenoid bone MP:0004458
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053828img abnormal sphenoid bone morphology MP:0000104
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053909img abnormal sphenoid bone morphology MP:0000104
Genes (22)

Species:
human : 22
SpeciesGeneGeneIdGene NameEvidence
HumanGSC145258goosecoid homeobox
Click here to display 24 evidence detail records.
HumanSCUBE180274signal peptide, CUB domain, EGF-like 1
INFERRED
HumanALX460529ALX homeobox 4
INFERRED
HumanBNC254796basonuclin 2
INFERRED
HumanALX18092ALX homeobox 1
Click here to display 24 evidence detail records.
HumanWNT17471wingless-type MMTV integration site family, member 1
INFERRED
HumanTGFB27042transforming growth factor, beta 2
INFERRED
HumanSMO6608smoothened, frizzled family receptor
INFERRED
HumanRARA5914retinoic acid receptor, alpha
Click here to display 24 evidence detail records.
HumanPRRX15396paired related homeobox 1
INFERRED
HumanOTX25015orthodenticle homeobox 2
Click here to display 24 evidence detail records.
HumanMN14330meningioma (disrupted in balanced translocation) 1
INFERRED
HumanGJA12697gap junction protein, alpha 1, 43kDa
Click here to display 24 evidence detail records.
HumanFOXC22303forkhead box C2 (MFH-1, mesenchyme forkhead 1)
Click here to display 24 evidence detail records.
HumanFGFR12260fibroblast growth factor receptor 1
Click here to display 24 evidence detail records.
HumanEDNRA1909endothelin receptor type A
Click here to display 24 evidence detail records.
HumanECE11889endothelin converting enzyme 1
INFERRED
HumanDLX61750distal-less homeobox 6
Click here to display 24 evidence detail records.
HumanDLX51749distal-less homeobox 5
Click here to display 24 evidence detail records.
HumanDLX21746distal-less homeobox 2
Click here to display 24 evidence detail records.
HumanDLX11745distal-less homeobox 1
Click here to display 24 evidence detail records.
HumanBMP7655bone morphogenetic protein 7
Click here to display 24 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003235abnormal alisphenoid bone morphology0self