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Details
Link-It Detail - Jax Mouse Phenotype - abnormal endochondral bone ossification
Debug Stats
  • ### Total Build Time: 35 ms 21.278 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 406 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 262 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=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 581 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.970 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.566 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=28 ms Completed: 28 ms rowSize= 15.201 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.177 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal endochondral bone ossification MP:0008272
Definition (1)
anomaly in the process of the formation of bone by the replacement of cartilage tissue with mineralized bone
Parents (1)
img abnormal bone ossification MP:0008271
Children (4)
img premature endochondral bone ossification MP:0003417
img failure of endochondral bone ossification MP:0008275
img delayed endochondral bone ossification MP:0003419
img abnormal sternum ossification MP:0008277
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053905img abnormal bone ossification MP:0008271
Genes (91)

Species:
human : 91
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCOMMD3-BMI1100532731
INFERRED
HumanAMER1139285APC membrane recruitment protein 1
Click here to display 29 evidence detail records.
HumanSP7121340Sp7 transcription factor
INFERRED
HumanTWIST2117581twist basic helix-loop-helix transcription factor 2
Click here to display 29 evidence detail records.
HumanFAT479633FAT atypical cadherin 4
Click here to display 29 evidence detail records.
HumanWDR1957728WD repeat domain 19
INFERRED
HumanVANGL257216VANGL planar cell polarity protein 2
INFERRED
HumanTWSG157045twisted gastrulation homolog 1 (Drosophila)
INFERRED
HumanFAM20C56975family with sequence similarity 20, member C
INFERRED
HumanINPP5E56623inositol polyphosphate-5-phosphatase, 72 kDa
INFERRED
HumanSMPD355512sphingomyelin phosphodiesterase 3, neutral membrane (neutral sphingomyelinase II)
INFERRED
HumanDPPA455211developmental pluripotency associated 4
INFERRED
HumanMKS154903Meckel syndrome, type 1
Click here to display 29 evidence detail records.
HumanFGFRL153834fibroblast growth factor receptor-like 1
INFERRED
HumanSUCO51430SUN domain containing ossification factor
INFERRED
HumanNSDHL50814NAD(P) dependent steroid dehydrogenase-like
INFERRED
HumanNIPBL25836Nipped-B homolog (Drosophila)
INFERRED
HumanSF3B123451splicing factor 3b, subunit 1, 155kDa
INFERRED
HumanDICER123405dicer 1, ribonuclease type III
INFERRED
HumanPDS5B23047PDS5, regulator of cohesion maintenance, homolog B (S. cerevisiae)
INFERRED
HumanKIF3A11127kinesin family member 3A
Click here to display 29 evidence detail records.
HumanKIAA05869786KIAA0586
Click here to display 29 evidence detail records.
HumanHDAC49759histone deacetylase 4
INFERRED
HumanPHF149678PHD finger protein 14
INFERRED
HumanHS2ST19653heparan sulfate 2-O-sulfotransferase 1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0008272abnormal endochondral bone ossification0self