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Details
Link-It Detail - Jax Mouse Phenotype - abnormal sternum ossification
Debug Stats
  • ### Total Build Time: 217 ms 23.612 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 386 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 274 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=36 ms Completed: 36 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=8 ms Completed: 8 ms rowSize= 1.033 KB
  • CONCEPT_CHILDREN gt=7 ms Completed: 7 ms rowSize= 588 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=19 ms Completed: 19 ms rowSize= 2.912 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=134 ms Completed: 134 ms rowSize= 17.137 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.167 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal sternum ossification MP:0008277
Definition (1)
anomaly in the process of the formation of the sternum bone by the replacement of cartilage tissue with mineralized bone
Parents (2)
img abnormal sternum morphology MP:0000157
img abnormal endochondral bone ossification MP:0008272
Children (1)
img failure of sternum ossification MP:0008278
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053907img abnormal sternum morphology MP:0000157
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053906img abnormal endochondral bone ossification MP:0008272
Genes (36)

Species:
human : 36
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SpeciesGeneGeneIdGene NameEvidence
HumanCOMMD3-BMI1100532731
Click here to display 45 evidence detail records.
HumanAMER1139285APC membrane recruitment protein 1
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HumanFAT479633FAT atypical cadherin 4
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HumanWDR1957728WD repeat domain 19
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HumanVANGL257216VANGL planar cell polarity protein 2
Click here to display 45 evidence detail records.
HumanSMPD355512sphingomyelin phosphodiesterase 3, neutral membrane (neutral sphingomyelinase II)
Click here to display 45 evidence detail records.
HumanDPPA455211developmental pluripotency associated 4
Click here to display 45 evidence detail records.
HumanFGFRL153834fibroblast growth factor receptor-like 1
Click here to display 45 evidence detail records.
HumanSF3B123451splicing factor 3b, subunit 1, 155kDa
Click here to display 45 evidence detail records.
HumanPDS5B23047PDS5, regulator of cohesion maintenance, homolog B (S. cerevisiae)
Click here to display 45 evidence detail records.
HumanPHF149678PHD finger protein 14
Click here to display 45 evidence detail records.
HumanHS2ST19653heparan sulfate 2-O-sulfotransferase 1
Click here to display 45 evidence detail records.
HumanALKBH18846alkB, alkylation repair homolog 1 (E. coli)
Click here to display 45 evidence detail records.
HumanDCHS18642dachsous 1 (Drosophila)
Click here to display 45 evidence detail records.
HumanPCGF27703polycomb group ring finger 2
Click here to display 45 evidence detail records.
HumanWHSC17468Wolf-Hirschhorn syndrome candidate 1
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HumanTRPS17227trichorhinophalangeal syndrome I
Click here to display 45 evidence detail records.
HumanSP36670Sp3 transcription factor
Click here to display 45 evidence detail records.
HumanSOX56660SRY (sex determining region Y)-box 5
Click here to display 45 evidence detail records.
HumanSIX16495SIX homeobox 1
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HumanRNF26045ring finger protein 2
Click here to display 45 evidence detail records.
HumanPTHLH5744parathyroid hormone-like hormone
Click here to display 45 evidence detail records.
HumanMYF64618myogenic factor 6 (herculin)
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HumanMYF54617myogenic factor 5
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HumanMLLT34300myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 3
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XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0008277abnormal sternum ossification0self