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Details
Link-It Detail - Jax Mouse Phenotype - abnormal cartilage development
Debug Stats
  • ### Total Build Time: 513 ms 24.369 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 388 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 374 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 181 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
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  • CONCEPT_PARENTS gt=15 ms Completed: 15 ms rowSize= 1.025 KB
  • CONCEPT_CHILDREN gt=11 ms Completed: 11 ms rowSize= 2.429 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=20 ms Completed: 20 ms rowSize= 2.904 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=454 ms Completed: 454 ms rowSize= 15.777 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 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 cartilage development MP:0000164
Definition (1)
anomaly in the formation of the nonvascular, resilient, flexible connective tissue found primarily in joints, walls of the thorax, and tubular structures, but which also comprises most of the skeleton in early fetal life
Synonyms (1)
"abnormal chondrogenesis" EXACT
Parents (2)
img abnormal cartilage morphology MP:0000163
img abnormal skeleton development MP:0002113
Children (5)
img abnormal long bone hypertrophic chondrocyte zone MP:0000165
img chondrodystrophy MP:0002657
img abnormal long bone epiphyseal plate proliferative zone MP:0003662
img abnormal intervertebral disk development MP:0005229
img abnormal synchondrosis MP:0004053
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053905img abnormal cartilage morphology MP:0000163
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053905img abnormal skeleton development MP:0002113
Genes (152)

Species:
human : 152
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMIA3375056melanoma inhibitory activity family, member 3
Click here to display 111 evidence detail records.
HumanSPRED2200734sprouty-related, EVH1 domain containing 2
INFERRED
HumanBMPER168667BMP binding endothelial regulator
Click here to display 111 evidence detail records.
HumanEVC2132884Ellis van Creveld syndrome 2
INFERRED
HumanTWIST2117581twist basic helix-loop-helix transcription factor 2
INFERRED
HumanPKDCC91461protein kinase domain containing, cytoplasmic
INFERRED
HumanSLC39A1391252solute carrier family 39 (zinc transporter), member 13
INFERRED
HumanCOL27A185301collagen, type XXVII, alpha 1
INFERRED
HumanHES784667hairy and enhancer of split 7 (Drosophila)
INFERRED
HumanOPA380207optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
INFERRED
HumanWLS79971wntless homolog (Drosophila)
INFERRED
HumanNABP279035nucleic acid binding protein 2
Click here to display 111 evidence detail records.
HumanCREB3L264764cAMP responsive element binding protein 3-like 2
INFERRED
HumanLEPRE164175leucine proline-enriched proteoglycan (leprecan) 1
INFERRED
HumanIFT8057560intraflagellar transport 80 homolog (Chlamydomonas)
INFERRED
HumanTWSG157045twisted gastrulation homolog 1 (Drosophila)
INFERRED
HumanFAM20C56975family with sequence similarity 20, member C
INFERRED
HumanKIAA121756243KIAA1217
INFERRED
HumanSULF255959sulfatase 2
INFERRED
HumanCSGALNACT155790chondroitin sulfate N-acetylgalactosaminyltransferase 1
INFERRED
HumanHHAT55733hedgehog acyltransferase
Click here to display 111 evidence detail records.
HumanSMPD355512sphingomyelin phosphodiesterase 3, neutral membrane (neutral sphingomyelinase II)
Click here to display 111 evidence detail records.
HumanIMPAD154928inositol monophosphatase domain containing 1
Click here to display 111 evidence detail records.
HumanDYM54808dymeclin
INFERRED
HumanMEX3C51320mex-3 RNA binding family member C
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000164abnormal cartilage development0self