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Details
Link-It Detail - Jax Mouse Phenotype - abnormal basicranium morphology
Debug Stats
  • ### Total Build Time: 130 ms 22.095 KB
  • CONCEPT_NAME gt=10 ms Completed: 10 ms rowSize= 390 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 293 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 180 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=11 ms Completed: 11 ms rowSize= 582 bytes
  • CONCEPT_CHILDREN gt=10 ms Completed: 10 ms rowSize= 1.497 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.904 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=91 ms Completed: 91 ms rowSize= 14.969 KB
  • CONCEPT_XREFS gt=6 ms Completed: 6 ms rowSize= 1.169 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal basicranium morphology MP:0010029
Definition (1)
any structural anomaly of the sloping floor of the cranial cavity that is comprised of parts of the ethmoidal, occipital and sphenoid bones
Synonyms (1)
"cranial base dysplasia" EXACT
Parents (1)
img abnormal cranium morphology MP:0000438
Children (3)
img abnormal basioccipital bone morphology MP:0000079
img abnormal basicranium angle MP:0009782
img abnormal basisphenoid bone morphology MP:0000106
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053826img abnormal cranium morphology MP:0000438
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053907img abnormal cranium morphology MP:0000438
Genes (67)

Species:
human : 67
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSH3PXD2B285590SH3 and PX domains 2B
Click here to display 35 evidence detail records.
HumanBMPER168667BMP binding endothelial regulator
INFERRED
HumanGSC145258goosecoid homeobox
Click here to display 35 evidence detail records.
HumanEVC2132884Ellis van Creveld syndrome 2
Click here to display 35 evidence detail records.
HumanPKDCC91461protein kinase domain containing, cytoplasmic
INFERRED
HumanDISP184976dispatched homolog 1 (Drosophila)
INFERRED
HumanTMEM10784314transmembrane protein 107
INFERRED
HumanALX460529ALX homeobox 4
Click here to display 35 evidence detail records.
HumanANKH56172ANKH inorganic pyrophosphate transport regulator
INFERRED
HumanSULF255959sulfatase 2
INFERRED
HumanHHAT55733hedgehog acyltransferase
INFERRED
HumanFGFRL153834fibroblast growth factor receptor-like 1
INFERRED
HumanCDON50937cell adhesion associated, oncogene regulated
INFERRED
HumanSMG123049SMG1 phosphatidylinositol 3-kinase-related kinase
INFERRED
HumanKIF3A11127kinesin family member 3A
Click here to display 35 evidence detail records.
HumanNOG9241noggin
Click here to display 35 evidence detail records.
HumanMBTPS18720membrane-bound transcription factor peptidase, site 1
Click here to display 35 evidence detail records.
HumanCHRD8646chordin
INFERRED
HumanALX18092ALX homeobox 1
INFERRED
HumanWNT9A7483wingless-type MMTV integration site family, member 9A
INFERRED
HumanWNT17471wingless-type MMTV integration site family, member 1
INFERRED
HumanTCF156939transcription factor 15 (basic helix-loop-helix)
INFERRED
HumanZEB16935zinc finger E-box binding homeobox 1
INFERRED
HumanTBX156913T-box 15
INFERRED
HumanTBX16899T-box 1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0010029abnormal basicranium morphology0self