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Details
Link-It Detail - Jax Mouse Phenotype - abnormal triploblastic development
Debug Stats
  • ### Total Build Time: 64 ms 22.857 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 396 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 221 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 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=4 ms Completed: 4 ms rowSize= 1.036 KB
  • CONCEPT_CHILDREN gt=1 ms Completed: 1 ms rowSize= 1.941 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 2.925 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=54 ms Completed: 54 ms rowSize= 15.036 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.172 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal triploblastic development MP:0001674
Definition (1)
abnormal development of the three primary germ layers of the embryo
Parents (2)
img abnormal developmental patterning MP:0002084
img abnormal embryonic tissue morphology MP:0002085
Children (4)
img abnormal endoderm development MP:0001685
img abnormal ectoderm development MP:0001675
img abnormal mesoderm development MP:0001680
img abnormal mesendoderm development MP:0009266
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img embryogenesis phenotype MP:00053805img abnormal developmental patterning MP:0002084
img mammalian phenotype MP:0000001img embryogenesis phenotype MP:00053805img abnormal embryonic tissue morphology MP:0002085
Genes (210)

Species:
human : 210
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSCXA100129885scleraxis homolog A (mouse)
INFERRED
HumanSCXB642658scleraxis homolog B (mouse)
INFERRED
HumanMSGN1343930mesogenin 1
INFERRED
HumanRSPO2340419R-spondin 2
INFERRED
HumanCRB2286204crumbs homolog 2 (Drosophila)
INFERRED
HumanSP8221833Sp8 transcription factor
INFERRED
HumanFLCN201163folliculin
INFERRED
HumanRDH10157506retinol dehydrogenase 10 (all-trans)
INFERRED
HumanMESP2145873mesoderm posterior 2 homolog (mouse)
INFERRED
HumanPRICKLE1144165prickle homolog 1 (Drosophila)
INFERRED
HumanWNT3A89780wingless-type MMTV integration site family, member 3A
INFERRED
HumanMIXL183881Mix paired-like homeobox
INFERRED
HumanATAD3B83858ATPase family, AAA domain containing 3B
INFERRED
HumanAMN81693amnion associated transmembrane protein
INFERRED
HumanFUZ80199fuzzy planar cell polarity protein
INFERRED
HumanWLS79971wntless homolog (Drosophila)
Click here to display 35 evidence detail records.
HumanPALB279728partner and localizer of BRCA2
INFERRED
HumanGNPNAT164841glucosamine-phosphate N-acetyltransferase 1
INFERRED
HumanPORCN64840porcupine homolog (Drosophila)
INFERRED
HumanSOX1764321SRY (sex determining region Y)-box 17
INFERRED
HumanEXOC460412exocyst complex component 4
INFERRED
HumanCHD857680chromodomain helicase DNA binding protein 8
INFERRED
HumanEPB41L557669erythrocyte membrane protein band 4.1 like 5
Click here to display 35 evidence detail records.
HumanSALL457167sal-like 4 (Drosophila)
INFERRED
HumanPOGLUT156983protein O-glucosyltransferase 1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001674abnormal triploblastic development0self