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Details
Link-It Detail - Jax Mouse Phenotype - abnormal primitive node morphology
Debug Stats
  • ### Total Build Time: 30 ms 20.347 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= 498 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 199 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=0 Completed: 0 ms rowSize= 591 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.026 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.581 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=26 ms Completed: 26 ms rowSize= 14.778 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.172 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal primitive node morphology MP:0004066
Definition (1)
any structural anomaly of the regional thickening of cells at the rostral tip of the vertebrate primitive streak through which gastrulating cells migrate anteriorly to form tissues in the future head and neck; this region organizes the formation of the three embryonic layers and establishes the longitudinal axis and the polarity of the embryo
Synonyms (1)
"abnormal Spemann's organizer morphology" RELATED
Parents (1)
img abnormal primitive streak morphology MP:0002231
Children (2)
img abnormal embryonic cilium morphology MP:0004131
img absent primitive node MP:0009331
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img embryogenesis phenotype MP:00053806img abnormal primitive streak morphology MP:0002231
Genes (48)

Species:
human : 48
Page Size
Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanNOTO344022notochord homeobox
Click here to display 26 evidence detail records.
HumanPIFO128344primary cilia formation
Click here to display 26 evidence detail records.
HumanMIXL183881Mix paired-like homeobox
INFERRED
HumanAMN81693amnion associated transmembrane protein
INFERRED
HumanBICC180114bicaudal C homolog 1 (Drosophila)
Click here to display 26 evidence detail records.
HumanTCTN279867tectonic family member 2
INFERRED
HumanTCTN179600tectonic family member 1
INFERRED
HumanWDR3557539WD repeat domain 35
INFERRED
HumanVANGL257216VANGL planar cell polarity protein 2
INFERRED
HumanSALL457167sal-like 4 (Drosophila)
INFERRED
HumanIFT12255764intraflagellar transport 122 homolog (Chlamydomonas)
INFERRED
HumanIFT5755081intraflagellar transport 57 homolog (Chlamydomonas)
INFERRED
HumanCCDC4055036coiled-coil domain containing 40
INFERRED
HumanMKS154903Meckel syndrome, type 1
INFERRED
HumanTRIM3351592tripartite motif containing 33
Click here to display 26 evidence detail records.
HumanDLL128514delta-like 1 (Drosophila)
Click here to display 26 evidence detail records.
HumanINTU27152inturned planar cell polarity protein
INFERRED
HumanINVS27130inversin
Click here to display 26 evidence detail records.
HumanB9D127077B9 protein domain 1
INFERRED
HumanIFT17226160intraflagellar transport 172 homolog (Chlamydomonas)
INFERRED
HumanTRAF3IP126146TNF receptor-associated factor 3 interacting protein 1
INFERRED
HumanC2CD326005C2 calcium-dependent domain containing 3
INFERRED
HumanPOFUT223275protein O-fucosyltransferase 2
INFERRED
HumanKIF3A11127kinesin family member 3A
Click here to display 26 evidence detail records.
HumanKIAA05869786KIAA0586
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004066abnormal primitive node morphology0self