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Details
Link-It Detail - Jax Mouse Phenotype - abnormal placenta development
Debug Stats
  • ### Total Build Time: 138 ms 21.561 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 386 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 257 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 188 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= 583 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.950 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.573 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=130 ms Completed: 130 ms rowSize= 15.345 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.167 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal placenta development MP:0001712
Definition (1)
malformed or incomplete differentiation of the organ of metabolic exchange between the fetus and mother
Synonyms (1)
"abnormal placental development" EXACT
Parents (1)
img abnormal placenta morphology MP:0001711
Children (4)
img abnormal ectoplacental cone morphology MP:0005032
img abnormal chorioallantoic fusion MP:0002824
img abnormal chorionic plate morphology MP:0004560
img abnormal decidualization MP:0003845
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img embryogenesis phenotype MP:00053806img abnormal placenta morphology MP:0001711
Genes (156)

Species:
human : 156
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSCXA100129885scleraxis homolog A (mouse)
INFERRED
HumanSCXB642658scleraxis homolog B (mouse)
INFERRED
HumanRTL1388015retrotransposon-like 1
Click here to display 66 evidence detail records.
HumanHMX3340784H6 family homeobox 3
INFERRED
HumanCRB2286204crumbs homolog 2 (Drosophila)
INFERRED
HumanDPH3285381diphthamide biosynthesis 3
INFERRED
HumanLAMA1284217laminin, alpha 1
INFERRED
HumanIPMK253430inositol polyphosphate multikinase
INFERRED
HumanCOMMD1150684copper metabolism (Murr1) domain containing 1
INFERRED
HumanE2F7144455E2F transcription factor 7
Click here to display 66 evidence detail records.
HumanWDR8384292WD repeat domain 83
Click here to display 66 evidence detail records.
HumanATAD3B83858ATPase family, AAA domain containing 3B
INFERRED
HumanESX180712ESX homeobox 1
Click here to display 66 evidence detail records.
HumanGNPNAT164841glucosamine-phosphate N-acetyltransferase 1
INFERRED
HumanEPB41L557669erythrocyte membrane protein band 4.1 like 5
INFERRED
HumanMIB157534mindbomb E3 ubiquitin protein ligase 1
INFERRED
HumanSUPT20H55578suppressor of Ty 20 homolog (S. cerevisiae)
INFERRED
HumanATAD3A55210ATPase family, AAA domain containing 3A
INFERRED
HumanRTEL151750regulator of telomere elongation helicase 1
INFERRED
HumanCHMP551510charged multivesicular body protein 5
INFERRED
HumanUBR551366ubiquitin protein ligase E3 component n-recognin 5
INFERRED
HumanCXXC130827CXXC finger protein 1
INFERRED
HumanDNMT3L29947DNA (cytosine-5-)-methyltransferase 3-like
INFERRED
HumanN6AMT129104N-6 adenine-specific DNA methyltransferase 1 (putative)
INFERRED
HumanSETD229072SET domain containing 2
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001712abnormal placenta development0self