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Details
Link-It Detail - Jax Mouse Phenotype - abnormal chondrocyte morphology
Debug Stats
  • ### Total Build Time: 356 ms 21.869 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 390 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 219 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 179 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 584 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 1.030 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 1.569 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=331 ms Completed: 331 ms rowSize= 16.616 KB
  • CONCEPT_XREFS gt=8 ms Completed: 8 ms rowSize= 1.169 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal chondrocyte morphology MP:0000166
Definition (1)
any structural anomaly of a polymorphic cell that forms cartilage
Synonyms (1)
"abnormal chondrocytes" BROAD
Parents (1)
img abnormal cartilage morphology MP:0000163
Children (2)
img decreased chondrocyte cell number MP:0000167
img increased chondrocyte number MP:0011692
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053905img abnormal cartilage morphology MP:0000163
Genes (75)

Species:
human : 75
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SpeciesGeneGeneIdGene NameEvidence
HumanMIA3375056melanoma inhibitory activity family, member 3
Click here to display 123 evidence detail records.
HumanPKDCC91461protein kinase domain containing, cytoplasmic
Click here to display 123 evidence detail records.
HumanCOL27A185301collagen, type XXVII, alpha 1
Click here to display 123 evidence detail records.
HumanDISP184976dispatched homolog 1 (Drosophila)
Click here to display 123 evidence detail records.
HumanGNPTAB79158N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
Click here to display 123 evidence detail records.
HumanCREB3L264764cAMP responsive element binding protein 3-like 2
INFERRED
HumanTNS364759tensin 3
INFERRED
HumanFAM20C56975family with sequence similarity 20, member C
Click here to display 123 evidence detail records.
HumanCYP26B156603cytochrome P450, family 26, subfamily B, polypeptide 1
Click here to display 123 evidence detail records.
HumanANKH56172ANKH inorganic pyrophosphate transport regulator
Click here to display 123 evidence detail records.
HumanSULF255959sulfatase 2
INFERRED
HumanDYM54808dymeclin
Click here to display 123 evidence detail records.
HumanDERL251009derlin 2
Click here to display 123 evidence detail records.
HumanSLC39A1423516solute carrier family 39 (zinc transporter), member 14
Click here to display 123 evidence detail records.
HumanSIK323387SIK family kinase 3
INFERRED
HumanNCDN23154neurochondrin
Click here to display 123 evidence detail records.
HumanSPG2023111spastic paraplegia 20 (Troyer syndrome)
Click here to display 123 evidence detail records.
HumanCHSY122856chondroitin sulfate synthase 1
Click here to display 123 evidence detail records.
HumanKIF3A11127kinesin family member 3A
Click here to display 123 evidence detail records.
HumanTRIP119321thyroid hormone receptor interactor 11
Click here to display 123 evidence detail records.
HumanPAPSS290603'-phosphoadenosine 5'-phosphosulfate synthase 2
Click here to display 123 evidence detail records.
HumanTNFSF118600tumor necrosis factor (ligand) superfamily, member 11
Click here to display 123 evidence detail records.
HumanGDF58200growth differentiation factor 5
INFERRED
HumanMIA8190melanoma inhibitory activity
Click here to display 123 evidence detail records.
HumanFGF238074fibroblast growth factor 23
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000166abnormal chondrocyte morphology0self