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Details
Link-It Detail - Jax Mouse Phenotype - abnormal supraoccipital bone morphology
Debug Stats
  • ### Total Build Time: 89 ms 22.192 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 406 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 322 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 187 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
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  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=9 ms Completed: 9 ms rowSize= 589 bytes
  • CONCEPT_CHILDREN gt=8 ms Completed: 8 ms rowSize= 1.021 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.918 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=59 ms Completed: 59 ms rowSize= 15.464 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.177 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal supraoccipital bone morphology MP:0000078
Definition (1)
any structural anomaly of the bone on the dorsal side of the great foramen of the skull, usually forming a part of the occipital in the adult, but distinct in the young
Synonyms (1)
"supraoccipital bone dysplasia" EXACT
Parents (1)
img abnormal occipital bone morphology MP:0005269
Children (2)
img small supraoccipital bone MP:0004444
img absent supraoccipital bone MP:0004443
Ancestral Roots
RootRoot Plus OneDepthParent
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 (28)

Species:
human : 28
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanBMPER168667BMP binding endothelial regulator
INFERRED
HumanSCUBE180274signal peptide, CUB domain, EGF-like 1
INFERRED
HumanWDR1957728WD repeat domain 19
INFERRED
HumanHHAT55733hedgehog acyltransferase
INFERRED
HumanMKS154903Meckel syndrome, type 1
Click here to display 21 evidence detail records.
HumanMTF222823metal response element binding transcription factor 2
Click here to display 21 evidence detail records.
HumanPSIP111168PC4 and SFRS1 interacting protein 1
INFERRED
HumanDMRT210655doublesex and mab-3 related transcription factor 2
INFERRED
HumanGTF2IRD19569GTF2I repeat domain containing 1
INFERRED
HumanALX18092ALX homeobox 1
Click here to display 21 evidence detail records.
HumanPCGF27703polycomb group ring finger 2
Click here to display 21 evidence detail records.
HumanWNT9A7483wingless-type MMTV integration site family, member 9A
Click here to display 21 evidence detail records.
HumanTCF156939transcription factor 15 (basic helix-loop-helix)
Click here to display 21 evidence detail records.
HumanTBX156913T-box 15
Click here to display 21 evidence detail records.
HumanSP36670Sp3 transcription factor
Click here to display 21 evidence detail records.
HumanRBL15933retinoblastoma-like 1 (p107)
Click here to display 21 evidence detail records.
HumanPRRX15396paired related homeobox 1
INFERRED
HumanNPR24882natriuretic peptide receptor B/guanylate cyclase B (atrionatriuretic peptide receptor B)
INFERRED
HumanMSX24488msh homeobox 2
INFERRED
HumanMN14330meningioma (disrupted in balanced translocation) 1
Click here to display 21 evidence detail records.
HumanLMX1B4010LIM homeobox transcription factor 1, beta
INFERRED
HumanHOXA33200homeobox A3
Click here to display 21 evidence detail records.
HumanGBX22637gastrulation brain homeobox 2
INFERRED
HumanFOXC22303forkhead box C2 (MFH-1, mesenchyme forkhead 1)
Click here to display 21 evidence detail records.
HumanDLX51749distal-less homeobox 5
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000078abnormal supraoccipital bone morphology0self