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Details
Link-It Detail - Jax Mouse Phenotype - abnormal conotruncus morphology
Debug Stats
  • ### Total Build Time: 25 ms 16.585 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 390 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 434 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 205 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=5 ms Completed: 5 ms rowSize= 585 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.036 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 1.583 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=12 ms Completed: 12 ms rowSize= 11.076 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.169 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal conotruncus morphology MP:0010583
Definition (1)
any structural anomaly of the distal portion of the bulbus cordis that will give rise to the conus cordis, which will give rise to the outflow regions of the ventricles, and the truncus arteriosus which will be divided into proximal ends of the ascending aorta and pulmonary trunk
Synonyms (1)
"abnormal bulbus cordis, rostral half morphology" EXACT
Parents (1)
img abnormal heart tube morphology MP:0000270
Children (2)
img abnormal conotruncus septation MP:0010584
img abnormal conotruncal ridge morphology MP:0010585
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img cardiovascular system phenotype MP:00053857img abnormal heart tube morphology MP:0000270
Genes (22)

Species:
human : 22
SpeciesGeneGeneIdGene NameEvidence
HumanGATA5140628GATA binding protein 5
INFERRED
HumanBMP1027302bone morphogenetic protein 10
INFERRED
HumanFOXP127086forkhead box P1
INFERRED
HumanHEY123462hairy/enhancer-of-split related with YRPW motif 1
INFERRED
HumanPDS5A23244PDS5, regulator of cohesion maintenance, homolog A (S. cerevisiae)
INFERRED
HumanALDH1A28854aldehyde dehydrogenase 1 family, member A2
INFERRED
HumanTLL17092tolloid-like 1
INFERRED
HumanTBX26909T-box 2
INFERRED
HumanTBX16899T-box 1
img Jax MP, Pubmed Id: 11971873, MOUSE PHENOTYPE ID: MGI:98493
HumanSSR16745signal sequence receptor, alpha
INFERRED
HumanSOX46659SRY (sex determining region Y)-box 4
INFERRED
HumanRXRA6256retinoid X receptor, alpha
INFERRED
HumanRARA5914retinoic acid receptor, alpha
INFERRED
HumanPKD15310polycystic kidney disease 1 (autosomal dominant)
INFERRED
HumanMEOX24223mesenchyme homeobox 2
INFERRED
HumanISL13670ISL LIM homeobox 1
INFERRED
HumanHSPG23339heparan sulfate proteoglycan 2
INFERRED
HumanHHEX3087hematopoietically expressed homeobox
INFERRED
HumanGATA42626GATA binding protein 4
INFERRED
HumanFGFR22263fibroblast growth factor receptor 2
INFERRED
HumanVCAN1462versican
INFERRED
HumanBMP4652bone morphogenetic protein 4
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0010583abnormal conotruncus morphology0self