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Details
Link-It Detail - Jax Mouse Phenotype - abnormal occipital bone morphology
Debug Stats
  • ### Total Build Time: 82 ms 24.712 KB
  • CONCEPT_NAME gt=12 ms Completed: 12 ms rowSize= 396 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 230 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 182 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=5 ms Completed: 5 ms rowSize= 587 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 3.773 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 2.914 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=52 ms Completed: 52 ms rowSize= 15.346 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.172 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal occipital bone morphology MP:0005269
Definition (1)
any structural anomaly of the bone at the lower, posterior part of the skull
Synonyms (1)
"occipital bone dysplasia" EXACT
Parents (1)
img abnormal neurocranium morphology MP:0000074
Children (8)
img small occipital bone MP:0004441
img abnormal basioccipital bone morphology MP:0000079
img occipital bone foramen MP:0004442
img absent occipital bone MP:0004440
img abnormal foramen magnum morphology MP:0010941
img abnormal supraoccipital bone morphology MP:0000078
img abnormal exoccipital bone morphology MP:0000080
img fusion of atlas and occipital bones MP:0010728
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 (71)

Species:
human : 71
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCOMMD3-BMI1100532731
INFERRED
HumanBMPER168667BMP binding endothelial regulator
INFERRED
HumanDISP184976dispatched homolog 1 (Drosophila)
Click here to display 31 evidence detail records.
HumanCBX284733chromobox homolog 2
INFERRED
HumanTMEM10784314transmembrane protein 107
INFERRED
HumanSCUBE180274signal peptide, CUB domain, EGF-like 1
INFERRED
HumanWDR1957728WD repeat domain 19
INFERRED
HumanANKH56172ANKH inorganic pyrophosphate transport regulator
INFERRED
HumanHHAT55733hedgehog acyltransferase
INFERRED
HumanMKS154903Meckel syndrome, type 1
Click here to display 31 evidence detail records.
HumanMBTD154799mbt domain containing 1
Click here to display 31 evidence detail records.
HumanFGFRL153834fibroblast growth factor receptor-like 1
Click here to display 31 evidence detail records.
HumanHECTD125831HECT domain containing E3 ubiquitin protein ligase 1
INFERRED
HumanKAT6B23522K(lysine) acetyltransferase 6B
Click here to display 31 evidence detail records.
HumanMTF222823metal response element binding transcription factor 2
Click here to display 31 evidence detail records.
HumanPSIP111168PC4 and SFRS1 interacting protein 1
Click here to display 31 evidence detail records.
HumanDMRT210655doublesex and mab-3 related transcription factor 2
INFERRED
HumanTSHZ110194teashirt zinc finger homeobox 1
INFERRED
HumanGTF2IRD19569GTF2I repeat domain containing 1
INFERRED
HumanNOG9241noggin
Click here to display 31 evidence detail records.
HumanTBX189096T-box 18
Click here to display 31 evidence detail records.
HumanCHRD8646chordin
INFERRED
HumanALX18092ALX homeobox 1
INFERRED
HumanPCGF27703polycomb group ring finger 2
Click here to display 31 evidence detail records.
HumanWNT9A7483wingless-type MMTV integration site family, member 9A
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0005269abnormal occipital bone morphology0self