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Details
Link-It Detail - Jax Mouse Phenotype - abnormal basioccipital bone morphology
Debug Stats
  • ### Total Build Time: 166 ms 26.512 KB
  • CONCEPT_NAME gt=8 ms Completed: 7 ms rowSize= 404 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 347 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 186 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=0 Completed: 0 ms rowSize= 1.032 KB
  • CONCEPT_CHILDREN gt=24 ms Completed: 24 ms rowSize= 1.490 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 5.597 KB
  • CONCEPT_RELATIONSHIPS gt=2 ms Completed: 2 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=126 ms Completed: 126 ms rowSize= 16.157 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.176 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal basioccipital bone morphology MP:0000079
Definition (1)
any structural anomaly of the basilar process of the occipital bone in the base of the cranium, frequently forming a direct part of the occipital in the adult, but usually distinct in the young
Synonyms (1)
"basioccipital bone dysplasia" EXACT
Parents (2)
img abnormal basicranium morphology MP:0010029
img abnormal occipital bone morphology MP:0005269
Children (3)
img small basioccipital bone MP:0004447
img absent basioccipital bone MP:0009609
img fusion of basioccipital and basisphenoid bone MP:0004572
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053827img abnormal basicranium morphology MP:0010029
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053908img abnormal basicranium morphology MP:0010029
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053828img abnormal occipital bone morphology MP:0005269
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053909img abnormal occipital bone morphology MP:0005269
Genes (26)

Species:
human : 26
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanTMEM10784314transmembrane protein 107
Click here to display 40 evidence detail records.
HumanANKH56172ANKH inorganic pyrophosphate transport regulator
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HumanHHAT55733hedgehog acyltransferase
INFERRED
HumanFGFRL153834fibroblast growth factor receptor-like 1
INFERRED
HumanCHRD8646chordin
INFERRED
HumanWNT9A7483wingless-type MMTV integration site family, member 9A
Click here to display 40 evidence detail records.
HumanTCF156939transcription factor 15 (basic helix-loop-helix)
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HumanTBX156913T-box 15
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HumanTBX16899T-box 1
INFERRED
HumanSKI6497v-ski avian sarcoma viral oncogene homolog
INFERRED
HumanRARG5916retinoic acid receptor, gamma
Click here to display 40 evidence detail records.
HumanRARB5915retinoic acid receptor, beta
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HumanRARA5914retinoic acid receptor, alpha
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HumanPSEN15663presenilin 1
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HumanLTBP14052latent transforming growth factor beta binding protein 1
INFERRED
HumanHOXD43233homeobox D4
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HumanHOXA33200homeobox A3
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HumanHOXA23199homeobox A2
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HumanHOXA13198homeobox A1
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HumanGLI22736GLI family zinc finger 2
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HumanEVC2121Ellis van Creveld syndrome
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HumanPHC21912polyhomeotic homolog 2 (Drosophila)
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HumanDLX51749distal-less homeobox 5
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HumanCDX11044caudal type homeobox 1
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HumanBMP7655bone morphogenetic protein 7
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XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000079abnormal basioccipital bone morphology0self