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Details
Link-It Detail - Jax Mouse Phenotype - abnormal thyroid cartilage morphology
Debug Stats
  • ### Total Build Time: 27 ms 17.580 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 402 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= 185 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= 594 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.934 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=25 ms Completed: 25 ms rowSize= 11.952 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.175 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal thyroid cartilage morphology MP:0002260
Definition (1)
any structural anomaly of the largest of the laryngeal cartilages
Synonyms (1)
"thyroid cartilage dysplasia" EXACT
Parents (1)
img abnormal laryngeal cartilage morphology MP:0002256
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053906img abnormal laryngeal cartilage morphology MP:0002256
img mammalian phenotype MP:0000001img respiratory system phenotype MP:00053886img abnormal laryngeal cartilage morphology MP:0002256
Genes (20)

Species:
human : 20
SpeciesGeneGeneIdGene NameEvidence
HumanBMPER168667BMP binding endothelial regulator
Click here to display 39 evidence detail records.
HumanFGFRL153834fibroblast growth factor receptor-like 1
Click here to display 39 evidence detail records.
HumanSATB223314SATB homeobox 2
Click here to display 39 evidence detail records.
HumanRAI110743retinoic acid induced 1
Click here to display 39 evidence detail records.
HumanALDH1A28854aldehyde dehydrogenase 1 family, member A2
Click here to display 39 evidence detail records.
HumanCHRD8646chordin
Click here to display 39 evidence detail records.
HumanWNT17471wingless-type MMTV integration site family, member 1
Click here to display 39 evidence detail records.
HumanTBX16899T-box 1
Click here to display 39 evidence detail records.
HumanSMO6608smoothened, frizzled family receptor
Click here to display 39 evidence detail records.
HumanRARA5914retinoic acid receptor, alpha
Click here to display 39 evidence detail records.
HumanPKD15310polycystic kidney disease 1 (autosomal dominant)
Click here to display 39 evidence detail records.
HumanPAX95083paired box 9
Click here to display 39 evidence detail records.
HumanHOXB33213homeobox B3
Click here to display 39 evidence detail records.
HumanHOXA33200homeobox A3
Click here to display 39 evidence detail records.
HumanFOXC12296forkhead box C1
Click here to display 39 evidence detail records.
HumanFBLN12192fibulin 1
Click here to display 39 evidence detail records.
HumanEYA12138eyes absent homolog 1 (Drosophila)
Click here to display 39 evidence detail records.
HumanDLX61750distal-less homeobox 6
Click here to display 39 evidence detail records.
HumanDLX51749distal-less homeobox 5
Click here to display 39 evidence detail records.
HumanBMP7655bone morphogenetic protein 7
Click here to display 39 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002260abnormal thyroid cartilage morphology0self