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Details
Link-It Detail - Jax Mouse Phenotype - abnormal epiphyseal plate morphology
Debug Stats
  • ### Total Build Time: 52 ms 21.335 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 400 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 301 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
  • 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=0 Completed: 0 ms rowSize= 584 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 1.061 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.569 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=51 ms Completed: 51 ms rowSize= 15.949 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.174 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal epiphyseal plate morphology MP:0006395
Definition (1)
any structural anomaly of the cartilaginous center of ossification on the bones permitting growth of the bone in both directions during development
Synonyms (1)
"abnormal epiphyseal cartilage" EXACT
Parents (1)
img abnormal skeleton development MP:0002113
Children (2)
img abnormal long bone epiphyseal plate morphology MP:0003055
img abnormal vertebral epiphyseal plate morphology MP:0006394
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053905img abnormal skeleton development MP:0002113
Genes (159)

Species:
human : 159
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanGSX1219409GS homeobox 1
INFERRED
HumanSPRED2200734sprouty-related, EVH1 domain containing 2
INFERRED
HumanEVC2132884Ellis van Creveld syndrome 2
INFERRED
HumanTWIST2117581twist basic helix-loop-helix transcription factor 2
Click here to display 45 evidence detail records.
HumanPKDCC91461protein kinase domain containing, cytoplasmic
INFERRED
HumanSLC39A1391252solute carrier family 39 (zinc transporter), member 13
Click here to display 45 evidence detail records.
HumanCOL27A185301collagen, type XXVII, alpha 1
Click here to display 45 evidence detail records.
HumanOPA380207optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
Click here to display 45 evidence detail records.
HumanCREB3L264764cAMP responsive element binding protein 3-like 2
INFERRED
HumanTNS364759tensin 3
INFERRED
HumanEBF264641early B-cell factor 2
INFERRED
HumanLEPRE164175leucine proline-enriched proteoglycan (leprecan) 1
INFERRED
HumanIFT8057560intraflagellar transport 80 homolog (Chlamydomonas)
INFERRED
HumanVANGL257216VANGL planar cell polarity protein 2
INFERRED
HumanTWSG157045twisted gastrulation homolog 1 (Drosophila)
INFERRED
HumanFAM20C56975family with sequence similarity 20, member C
Click here to display 45 evidence detail records.
HumanSULF255959sulfatase 2
INFERRED
HumanCSGALNACT155790chondroitin sulfate N-acetylgalactosaminyltransferase 1
INFERRED
HumanSMPD355512sphingomyelin phosphodiesterase 3, neutral membrane (neutral sphingomyelinase II)
Click here to display 45 evidence detail records.
HumanIMPAD154928inositol monophosphatase domain containing 1
INFERRED
HumanDYM54808dymeclin
INFERRED
HumanFGFRL153834fibroblast growth factor receptor-like 1
INFERRED
HumanMEX3C51320mex-3 RNA binding family member C
INFERRED
HumanCHST1150515carbohydrate (chondroitin 4) sulfotransferase 11
Click here to display 45 evidence detail records.
HumanSMARCAL150485SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0006395abnormal epiphyseal plate morphology0self