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Details
Link-It Detail - Jax Mouse Phenotype - abnormal temporal bone morphology
Debug Stats
  • ### Total Build Time: 54 ms 22.858 KB
  • CONCEPT_NAME gt=11 ms Completed: 11 ms rowSize= 394 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 314 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=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=5 ms Completed: 5 ms rowSize= 587 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.946 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.914 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=32 ms Completed: 32 ms rowSize= 15.241 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.171 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal temporal bone morphology MP:0005272
Definition (1)
any structural anomaly of the large, irregular bone located at the base and side of the skull; consists of three parts at birth: squamous, tympanic, and petrous
Synonyms (1)
"temporal bone dysplasia" EXACT
Parents (1)
img abnormal neurocranium morphology MP:0000074
Children (4)
img abnormal styloid process morphology MP:0008023
img abnormal squamosal bone morphology MP:0004423
img abnormal subarcuate fossa morphology MP:0009822
img small temporal bone MP:0004422
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 (44)

Species:
human : 44
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanRSPO2340419R-spondin 2
INFERRED
HumanBMPER168667BMP binding endothelial regulator
INFERRED
HumanSCUBE180274signal peptide, CUB domain, EGF-like 1
INFERRED
HumanALX460529ALX homeobox 4
INFERRED
HumanANKH56172ANKH inorganic pyrophosphate transport regulator
Click here to display 25 evidence detail records.
HumanHECTD125831HECT domain containing E3 ubiquitin protein ligase 1
Click here to display 25 evidence detail records.
HumanSATB223314SATB homeobox 2
Click here to display 25 evidence detail records.
HumanNOG9241noggin
INFERRED
HumanCHRD8646chordin
INFERRED
HumanPRKRA8575protein kinase, interferon-inducible double stranded RNA dependent activator
Click here to display 25 evidence detail records.
HumanALX18092ALX homeobox 1
INFERRED
HumanWNT17471wingless-type MMTV integration site family, member 1
INFERRED
HumanTWIST17291twist basic helix-loop-helix transcription factor 1
Click here to display 25 evidence detail records.
HumanTGFB27042transforming growth factor, beta 2
INFERRED
HumanTCOF16949Treacher Collins-Franceschetti syndrome 1
Click here to display 25 evidence detail records.
HumanTBX156913T-box 15
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HumanTBX16899T-box 1
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HumanSMO6608smoothened, frizzled family receptor
Click here to display 25 evidence detail records.
HumanSIX16495SIX homeobox 1
INFERRED
HumanRARA5914retinoic acid receptor, alpha
INFERRED
HumanPOU3F45456POU class 3 homeobox 4
Click here to display 25 evidence detail records.
HumanPOU3F35455POU class 3 homeobox 3
INFERRED
HumanPRRX15396paired related homeobox 1
INFERRED
HumanPHEX5251phosphate regulating endopeptidase homolog, X-linked
Click here to display 25 evidence detail records.
HumanPBX15087pre-B-cell leukemia homeobox 1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0005272abnormal temporal bone morphology0self