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Details
Link-It Detail - Jax Mouse Phenotype - complete atrioventricular septal defect
Debug Stats
  • ### Total Build Time: 70 ms 15.843 KB
  • CONCEPT_NAME gt=8 ms Completed: 8 ms rowSize= 406 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 446 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 182 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=0 Completed: 0 ms rowSize= 585 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 1.058 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.583 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=50 ms Completed: 50 ms rowSize= 10.300 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.177 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
complete atrioventricular septal defect MP:0010413
Definition (1)
a type of atrioventricular septal defect in which a single atrioventricular valve annulus, a common atrioventricular valve, and a defect of the inlet ventricular septum are observed; deficiency of the atrioventricular septum also results in the presence of a large primum atrial septal defect
Synonyms (1)
"complete common AV canal" EXACT
Parents (1)
img atrioventricular septal defect MP:0010412
Children (2)
img balanced complete atrioventricular canal MP:0011671
img unbalanced complete common atrioventricular canal MP:0011673
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img cardiovascular system phenotype MP:00053858img atrioventricular septal defect MP:0010412
Genes (17)

Species:
human : 17
SpeciesGeneGeneIdGene NameEvidence
HumanGATA5140628GATA binding protein 5
Click here to display 37 evidence detail records.
HumanHSPB1151668heat shock protein family B (small), member 11
INFERRED
HumanIFT17226160intraflagellar transport 172 homolog (Chlamydomonas)
Click here to display 37 evidence detail records.
HumanZFPM223414zinc finger protein, FOG family member 2
Click here to display 37 evidence detail records.
HumanPDS5A23244PDS5, regulator of cohesion maintenance, homolog A (S. cerevisiae)
Click here to display 37 evidence detail records.
HumanPDS5B23047PDS5, regulator of cohesion maintenance, homolog B (S. cerevisiae)
Click here to display 37 evidence detail records.
HumanSRSF1010772serine/arginine-rich splicing factor 10
Click here to display 37 evidence detail records.
HumanLEFTY110637left-right determination factor 1
Click here to display 37 evidence detail records.
HumanFOXH18928forkhead box H1
Click here to display 37 evidence detail records.
HumanLEFTY27044left-right determination factor 2
Click here to display 37 evidence detail records.
HumanTGFB27042transforming growth factor, beta 2
Click here to display 37 evidence detail records.
HumanRXRA6256retinoid X receptor, alpha
Click here to display 37 evidence detail records.
HumanCYR613491cysteine-rich, angiogenic inducer, 61
Click here to display 37 evidence detail records.
HumanGPC32719glypican 3
Click here to display 37 evidence detail records.
HumanGDF12657growth differentiation factor 1
Click here to display 37 evidence detail records.
HumanGATA42626GATA binding protein 4
Click here to display 37 evidence detail records.
HumanMEGF81954multiple EGF-like-domains 8
Click here to display 37 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0010413complete atrioventricular septal defect0self