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Details
Link-It Detail - Jax Mouse Phenotype - abnormal telencephalon development
Debug Stats
  • ### Total Build Time: 565 ms 27.144 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 396 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 250 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=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=15 ms Completed: 15 ms rowSize= 1.030 KB
  • CONCEPT_CHILDREN gt=91 ms Completed: 91 ms rowSize= 4.279 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=31 ms Completed: 31 ms rowSize= 2.921 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=417 ms Completed: 417 ms rowSize= 16.966 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 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 telencephalon development MP:0000934
Definition (1)
malformed or incomplete differentiation of the anterior division of the embryonic prosencephalon
Parents (2)
img abnormal telencephalon morphology MP:0000787
img abnormal forebrain development MP:0003232
Children (9)
img abnormal pallium development MP:0004171
img small embryonic telencephalon MP:0000936
img abnormal cortical ventricular zone morphology MP:0008458
img abnormal cortical marginal zone morphology MP:0000792
img abnormal subpallium development MP:0004172
img abnormal subplate morphology MP:0008440
img abnormal folding of telencephalic vesicles MP:0000935
img abnormal cortical intermediate zone morphology MP:0008457
img abnormal cortical plate morphology MP:0008439
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036317img abnormal telencephalon morphology MP:0000787
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036317img abnormal forebrain development MP:0003232
Genes (109)

Species:
human : 109
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanLHX8431707LIM homeobox 8
Click here to display 91 evidence detail records.
HumanINSC387755inscuteable homolog (Drosophila)
INFERRED
HumanFBXO45200933F-box protein 45
Click here to display 91 evidence detail records.
HumanGSX2170825GS homeobox 2
Click here to display 91 evidence detail records.
HumanARX170302aristaless related homeobox
Click here to display 91 evidence detail records.
HumanTTL150465tubulin tyrosine ligase
Click here to display 91 evidence detail records.
HumanZIC585416Zic family member 5
Click here to display 91 evidence detail records.
HumanLMNB284823lamin B2
INFERRED
HumanTCF7L183439transcription factor 7-like 1 (T-cell specific, HMG-box)
INFERRED
HumanNDEL181565nudE neurodevelopment protein 1-like 1
Click here to display 91 evidence detail records.
HumanPGAP180055post-GPI attachment to proteins 1
Click here to display 91 evidence detail records.
HumanMCPH179648microcephalin 1
INFERRED
HumanTCTN179600tectonic family member 1
INFERRED
HumanMLST864223MTOR associated protein, LST8 homolog (S. cerevisiae)
Click here to display 91 evidence detail records.
HumanNEUROD663974neuronal differentiation 6
Click here to display 91 evidence detail records.
HumanNEUROG263973neurogenin 2
Click here to display 91 evidence detail records.
HumanPTBP258155polypyrimidine tract binding protein 2
INFERRED
HumanTWSG157045twisted gastrulation homolog 1 (Drosophila)
Click here to display 91 evidence detail records.
HumanCTNNBIP156998catenin, beta interacting protein 1
Click here to display 91 evidence detail records.
HumanPARD356288par-3 family cell polarity regulator
Click here to display 91 evidence detail records.
HumanHHAT55733hedgehog acyltransferase
Click here to display 91 evidence detail records.
HumanCHD755636chromodomain helicase DNA binding protein 7
Click here to display 91 evidence detail records.
HumanAMBRA155626autophagy/beclin-1 regulator 1
Click here to display 91 evidence detail records.
HumanFBXW755294F-box and WD repeat domain containing 7, E3 ubiquitin protein ligase
INFERRED
HumanFEZF255079FEZ family zinc finger 2
Click here to display 91 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000934abnormal telencephalon development0self