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Details
Link-It Detail - Jax Mouse Phenotype - aorticopulmonary septal defect
Debug Stats
  • ### Total Build Time: 49 ms 20.718 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 388 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 346 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 162 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=8 ms Completed: 8 ms rowSize= 598 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 1.477 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 1.596 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=28 ms Completed: 28 ms rowSize= 14.874 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.168 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
aorticopulmonary septal defect MP:0010651
Definition (1)
an abnormal communication in the septum between the aorta and pulmonary artery, resulting from incomplete separation of the common tube of the truncus arteriosus and the aorticopulmonary trunk
Synonyms (1)
"APSD" EXACT
Parents (1)
img abnormal aorticopulmonary septum morphology MP:0010650
Children (3)
img persistent truncus arteriosis MP:0002633
img aortopulmonary window MP:0010455
img absent aorticopulmonary septum MP:0010652
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img cardiovascular system phenotype MP:00053857img abnormal aorticopulmonary septum morphology MP:0010650
Genes (51)

Species:
human : 51
Page Size
Current 25
  Page 1 of 3
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanRDH10157506retinol dehydrogenase 10 (all-trans)
INFERRED
HumanFUZ80199fuzzy planar cell polarity protein
INFERRED
HumanNXN64359nucleoredoxin
INFERRED
HumanMKL257496MKL/myocardin-like 2
INFERRED
HumanMESP155897mesoderm posterior 1 homolog (mouse)
INFERRED
HumanPARVA55742parvin, alpha
INFERRED
HumanFOXP127086forkhead box P1
INFERRED
HumanFOXD327022forkhead box D3
INFERRED
HumanDICER123405dicer 1, ribonuclease type III
INFERRED
HumanPDS5A23244PDS5, regulator of cohesion maintenance, homolog A (S. cerevisiae)
INFERRED
HumanPLXND123129plexin D1
INFERRED
HumanATE111101arginyltransferase 1
INFERRED
HumanSEMA3C10512sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C
INFERRED
HumanCITED210370Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2
INFERRED
HumanECE29718endothelin converting enzyme 2
INFERRED
HumanHAND29464heart and neural crest derivatives expressed 2
INFERRED
HumanALDH1A28854aldehyde dehydrogenase 1 family, member A2
INFERRED
HumanNRP18829neuropilin 1
INFERRED
HumanADAM198728ADAM metallopeptidase domain 19
INFERRED
HumanCHRD8646chordin
INFERRED
HumanIFT888100intraflagellar transport 88 homolog (Chlamydomonas)
INFERRED
HumanVEGFA7422vascular endothelial growth factor A
INFERRED
HumanTFAP2A7020transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
INFERRED
HumanTBX16899T-box 1
INFERRED
HumanSSR16745signal sequence receptor, alpha
img Jax MP, Pubmed Id: 17015483, MOUSE PHENOTYPE ID: MGI:105082
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0010651aorticopulmonary septal defect0self