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Details
Link-It Detail - Jax Mouse Phenotype - abnormal fontanelle morphology
Debug Stats
  • ### Total Build Time: 44 ms 21.152 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 388 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 247 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 178 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=14 ms Completed: 14 ms rowSize= 1.028 KB
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 582 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 4.250 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=23 ms Completed: 23 ms rowSize= 13.199 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.168 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal fontanelle morphology MP:0000084
Definition (1)
any structural anomaly in the membranous interval at the margins of cranial bones in neonates
Synonyms (1)
"fontanelle dysplasia" EXACT
Parents (2)
img abnormal neurocranium morphology MP:0000074
img abnormal skeleton development MP:0002113
Children (1)
img large anterior fontanelle MP:0000085
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
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053905img abnormal skeleton development MP:0002113
Genes (23)

Species:
human : 23
SpeciesGeneGeneIdGene NameEvidence
HumanTWIST2117581twist basic helix-loop-helix transcription factor 2
Click here to display 28 evidence detail records.
HumanALX460529ALX homeobox 4
Click here to display 28 evidence detail records.
HumanMKS154903Meckel syndrome, type 1
Click here to display 28 evidence detail records.
HumanBNC254796basonuclin 2
Click here to display 28 evidence detail records.
HumanSIK323387SIK family kinase 3
Click here to display 28 evidence detail records.
HumanTHRB7068thyroid hormone receptor, beta
Click here to display 28 evidence detail records.
HumanTHRA7067thyroid hormone receptor, alpha
Click here to display 28 evidence detail records.
HumanTGFB27042transforming growth factor, beta 2
INFERRED
HumanTFPI7035tissue factor pathway inhibitor (lipoprotein-associated coagulation inhibitor)
Click here to display 28 evidence detail records.
HumanRPS6KA36197ribosomal protein S6 kinase, 90kDa, polypeptide 3
Click here to display 28 evidence detail records.
HumanMSX14487msh homeobox 1
INFERRED
HumanMMP144323matrix metallopeptidase 14 (membrane-inserted)
Click here to display 28 evidence detail records.
HumanLMX1B4010LIM homeobox transcription factor 1, beta
Click here to display 28 evidence detail records.
HumanGSK3B2932glycogen synthase kinase 3 beta
Click here to display 28 evidence detail records.
HumanDNMT3B1789DNA (cytosine-5-)-methyltransferase 3 beta
INFERRED
HumanDLX51749distal-less homeobox 5
Click here to display 28 evidence detail records.
HumanCTSK1513cathepsin K
Click here to display 28 evidence detail records.
HumanCREBBP1387CREB binding protein
INFERRED
HumanRUNX2860runt-related transcription factor 2
Click here to display 28 evidence detail records.
HumanBMP7655bone morphogenetic protein 7
INFERRED
HumanATR545ataxia telangiectasia and Rad3 related
Click here to display 28 evidence detail records.
HumanATF4468activating transcription factor 4
Click here to display 28 evidence detail records.
HumanAES166amino-terminal enhancer of split
Click here to display 28 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000084abnormal fontanelle morphology0self