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Details
Link-It Detail - Jax Mouse Phenotype - abnormal cerebral cortex morphology
Debug Stats
  • ### Total Build Time: 3,299 ms 26.017 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 398 bytes
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  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 175 bytes
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  • CONCEPT_CHILDREN gt=30 ms Completed: 30 ms rowSize= 5.172 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.574 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=3,251 ms Completed: 3.251 Seconds rowSize= 16.455 KB
  • CONCEPT_XREFS gt=9 ms Completed: 9 ms rowSize= 1.173 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal cerebral cortex morphology MP:0000788
Definition (1)
any structural anomaly of thin layer of grey matter on the surface of the cerebral hemisphere that develops from the telencephalon and folds into gyri; it is responsible for intellectual faculties and higher mental functions
Synonyms (1)
"pallium dysplasia" EXACT
Parents (1)
img abnormal cerebrum morphology MP:0008540
Children (11)
img delaminated cerebral cortex MP:0000791
img abnormal cingulate gyrus morphology MP:0004167
img abnormal neocortex morphology MP:0008547
img abnormal orbitofrontal cortex morphology MP:0004170
img abnormal stratification in cerebral cortex MP:0000790
img thickened cerebral cortex MP:0000789
img abnormal somatosensory cortex morphology MP:0000859
img abnormal cerebral cortex pyramidal cell morphology MP:0009969
img loss of cortex neurons MP:0003241
img abnormal visual cortex morphology MP:0000805
img thin cerebral cortex MP:0006254
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036318img abnormal cerebrum morphology MP:0008540
Genes (249)

Species:
human : 249
Page Size
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SpeciesGeneGeneIdGene NameEvidence
HumanINSC387755inscuteable homolog (Drosophila)
Click here to display 295 evidence detail records.
HumanLRRTM1347730leucine rich repeat transmembrane neuronal 1
INFERRED
HumanASPM259266asp (abnormal spindle) homolog, microcephaly associated (Drosophila)
INFERRED
HumanARX170302aristaless related homeobox
Click here to display 295 evidence detail records.
HumanESCO2157570establishment of sister chromatid cohesion N-acetyltransferase 2
INFERRED
HumanRDH10157506retinol dehydrogenase 10 (all-trans)
Click here to display 295 evidence detail records.
HumanGDF7151449growth differentiation factor 7
Click here to display 295 evidence detail records.
HumanTTL150465tubulin tyrosine ligase
INFERRED
HumanAK7122481adenylate kinase 7
INFERRED
HumanARHGAP33115703Rho GTPase activating protein 33
Click here to display 295 evidence detail records.
HumanPLXNA491584plexin A4
INFERRED
HumanZIC585416Zic family member 5
Click here to display 295 evidence detail records.
HumanLMNB284823lamin B2
Click here to display 295 evidence detail records.
HumanSLX484464SLX4 structure-specific endonuclease subunit
Click here to display 295 evidence detail records.
HumanARL684100ADP-ribosylation factor-like 6
INFERRED
HumanJAM383700junctional adhesion molecule 3
Click here to display 295 evidence detail records.
HumanMCPH179648microcephalin 1
INFERRED
HumanFKRP79147fukutin related protein
Click here to display 295 evidence detail records.
HumanMARCKSL165108MARCKS-like 1
INFERRED
HumanPINK165018PTEN induced putative kinase 1
Click here to display 295 evidence detail records.
HumanMPP564398membrane protein, palmitoylated 5 (MAGUK p55 subfamily member 5)
Click here to display 295 evidence detail records.
HumanNPAS364067neuronal PAS domain protein 3
Click here to display 295 evidence detail records.
HumanNEUROD663974neuronal differentiation 6
INFERRED
HumanZNF33563925zinc finger protein 335
INFERRED
HumanUSE155850unconventional SNARE in the ER 1 homolog (S. cerevisiae)
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000788abnormal cerebral cortex morphology0self