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Details
Link-It Detail - Jax Mouse Phenotype - abnormal neural fold formation
Debug Stats
  • ### Total Build Time: 43 ms 20.916 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 388 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 293 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 190 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=3 ms Completed: 3 ms rowSize= 586 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 597 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 1.576 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=34 ms Completed: 34 ms rowSize= 16.021 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.168 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal neural fold formation MP:0004837
Definition (1)
any anomaly in the process by which the edges of the neural plate thicken and move up to form a U-shaped structure called the neural groove
Synonyms (1)
"abnormal neural groove formation" EXACT
Parents (1)
img abnormal neural fold morphology MP:0011256
Children (1)
img abnormal neural fold elevation formation MP:0004838
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img embryogenesis phenotype MP:00053806img abnormal neural fold morphology MP:0011256
Genes (33)

Species:
human : 33
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Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanDISP184976dispatched homolog 1 (Drosophila)
Click here to display 25 evidence detail records.
HumanMIXL183881Mix paired-like homeobox
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HumanTCF7L183439transcription factor 7-like 1 (T-cell specific, HMG-box)
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HumanGRHL279977grainyhead-like 2 (Drosophila)
INFERRED
HumanPOGLUT156983protein O-glucosyltransferase 1
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HumanMESP155897mesoderm posterior 1 homolog (mouse)
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HumanAMBRA155626autophagy/beclin-1 regulator 1
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HumanHECTD125831HECT domain containing E3 ubiquitin protein ligase 1
INFERRED
HumanFLRT323767fibronectin leucine rich transmembrane protein 3
INFERRED
HumanGPR16123432G protein-coupled receptor 161
Click here to display 25 evidence detail records.
HumanCITED210370Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2
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HumanHAP19001huntingtin-associated protein 1
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HumanFOXH18928forkhead box H1
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HumanBCL108915B-cell CLL/lymphoma 10
INFERRED
HumanLMO48543LIM domain only 4
INFERRED
HumanZIC27546Zic family member 2
Click here to display 25 evidence detail records.
HumanTCOF16949Treacher Collins-Franceschetti syndrome 1
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HumanT6862T, brachyury homolog (mouse)
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HumanSTK116794serine/threonine kinase 11
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HumanSMO6608smoothened, frizzled family receptor
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HumanSMARCC16599SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1
INFERRED
HumanSALL26297sal-like 2 (Drosophila)
INFERRED
HumanPOR5447P450 (cytochrome) oxidoreductase
INFERRED
HumanPAX35077paired box 3
INFERRED
HumanNODAL4838nodal growth differentiation factor
Click here to display 25 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004837abnormal neural fold formation0self