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Details
Link-It Detail - Jax Mouse Phenotype - abnormal sphenoid bone morphology
Debug Stats
  • ### Total Build Time: 86 ms 22.501 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 394 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 232 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=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=11 ms Completed: 11 ms rowSize= 587 bytes
  • CONCEPT_CHILDREN gt=12 ms Completed: 12 ms rowSize= 2.434 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=17 ms Completed: 17 ms rowSize= 2.914 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=39 ms Completed: 39 ms rowSize= 14.477 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.171 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal sphenoid bone morphology MP:0000104
Definition (1)
any structural anomaly of the irregularly shaped bone of the base of the skull
Synonyms (1)
"sphenoid bone dysplasia" EXACT
Parents (1)
img abnormal neurocranium morphology MP:0000074
Children (5)
img abnormal orbitosphenoid bone morphology MP:0004457
img abnormal pterygoid process morphology MP:0004452
img abnormal basisphenoid bone morphology MP:0000106
img abnormal presphenoid bone morphology MP:0004448
img abnormal alisphenoid bone morphology MP:0003235
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053827img abnormal neurocranium morphology MP:0000074
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053908img abnormal neurocranium morphology MP:0000074
Genes (67)

Species:
human : 67
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanBMPER168667BMP binding endothelial regulator
INFERRED
HumanGSC145258goosecoid homeobox
INFERRED
HumanPKDCC91461protein kinase domain containing, cytoplasmic
INFERRED
HumanDISP184976dispatched homolog 1 (Drosophila)
INFERRED
HumanTMEM10784314transmembrane protein 107
INFERRED
HumanARID5B84159AT rich interactive domain 5B (MRF1-like)
INFERRED
HumanSCUBE180274signal peptide, CUB domain, EGF-like 1
INFERRED
HumanCSRNP164651cysteine-serine-rich nuclear protein 1
INFERRED
HumanALX460529ALX homeobox 4
INFERRED
HumanSULF255959sulfatase 2
INFERRED
HumanMKS154903Meckel syndrome, type 1
INFERRED
HumanBNC254796basonuclin 2
INFERRED
HumanFGFRL153834fibroblast growth factor receptor-like 1
Click here to display 15 evidence detail records.
HumanCDON50937cell adhesion associated, oncogene regulated
INFERRED
HumanSCHIP129970schwannomin interacting protein 1
INFERRED
HumanTIPARP25976TCDD-inducible poly(ADP-ribose) polymerase
INFERRED
HumanNIPBL25836Nipped-B homolog (Drosophila)
Click here to display 15 evidence detail records.
HumanKIF3A11127kinesin family member 3A
INFERRED
HumanHAND29464heart and neural crest derivatives expressed 2
INFERRED
HumanSGPL18879sphingosine-1-phosphate lyase 1
INFERRED
HumanCHRD8646chordin
INFERRED
HumanLMO48543LIM domain only 4
Click here to display 15 evidence detail records.
HumanALX18092ALX homeobox 1
INFERRED
HumanWNT17471wingless-type MMTV integration site family, member 1
INFERRED
HumanTGFB27042transforming growth factor, beta 2
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000104abnormal sphenoid bone morphology0self