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Details
Link-It Detail - Jax Mouse Phenotype - abnormal neocortex morphology
Debug Stats
  • ### Total Build Time: 55 ms 21.471 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 386 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 197 bytes
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  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
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  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=46 ms Completed: 46 ms rowSize= 17.095 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.167 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal neocortex morphology MP:0008547
Definition (1)
any structural anomaly of the larger part of the mammalian cerebral cortex, distinguished from the allocortex by being composed of a larger number of nerve cells arranged in six layers
Synonyms (1)
"abnormal nonolfactory cortex morphology" EXACT
Parents (1)
img abnormal cerebral cortex morphology MP:0000788
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036319img abnormal cerebral cortex morphology MP:0000788
Genes (30)

Species:
human : 30
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SpeciesGeneGeneIdGene NameEvidence
HumanASPM259266asp (abnormal spindle) homolog, microcephaly associated (Drosophila)
Click here to display 43 evidence detail records.
HumanARX170302aristaless related homeobox
Click here to display 43 evidence detail records.
HumanESCO2157570establishment of sister chromatid cohesion N-acetyltransferase 2
Click here to display 43 evidence detail records.
HumanARHGAP33115703Rho GTPase activating protein 33
Click here to display 43 evidence detail records.
HumanMCPH179648microcephalin 1
Click here to display 43 evidence detail records.
HumanCCDC88A55704coiled-coil domain containing 88A
Click here to display 43 evidence detail records.
HumanCHD755636chromodomain helicase DNA binding protein 7
Click here to display 43 evidence detail records.
HumanFEZF255079FEZ family zinc finger 2
Click here to display 43 evidence detail records.
HumanMKS154903Meckel syndrome, type 1
Click here to display 43 evidence detail records.
HumanPOMT229954protein-O-mannosyltransferase 2
Click here to display 43 evidence detail records.
HumanCADM123705cell adhesion molecule 1
Click here to display 43 evidence detail records.
HumanCUX223316cut-like homeobox 2
Click here to display 43 evidence detail records.
HumanZBTB1810472zinc finger and BTB domain containing 18
Click here to display 43 evidence detail records.
HumanLHX29355LIM homeobox 2
Click here to display 43 evidence detail records.
HumanPEX11B8799peroxisomal biogenesis factor 11 beta
Click here to display 43 evidence detail records.
HumanTSC17248tuberous sclerosis 1
Click here to display 43 evidence detail records.
HumanPROS15627protein S (alpha)
Click here to display 43 evidence detail records.
HumanPOU3F25454POU class 3 homeobox 2
Click here to display 43 evidence detail records.
HumanPAFAH1B15048platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa)
Click here to display 43 evidence detail records.
HumanNPC14864Niemann-Pick disease, type C1
Click here to display 43 evidence detail records.
HumanID43400inhibitor of DNA binding 4, dominant negative helix-loop-helix protein
Click here to display 43 evidence detail records.
HumanFOXC12296forkhead box C1
Click here to display 43 evidence detail records.
HumanFOXG12290forkhead box G1
Click here to display 43 evidence detail records.
HumanFGF12246fibroblast growth factor 1 (acidic)
Click here to display 43 evidence detail records.
HumanESR22100estrogen receptor 2 (ER beta)
Click here to display 43 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0008547abnormal neocortex morphology0self