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Details
Link-It Detail - Jax Mouse Phenotype - abnormal corticospinal tract morphology
Debug Stats
  • ### Total Build Time: 27 ms 12.510 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 406 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= 193 bytes
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  • CONCEPT_GENES gt=22 ms Completed: 22 ms rowSize= 7.971 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.177 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal corticospinal tract morphology MP:0002878
Definition (1)
any structural anomaly of the corticospinal fibers that arise from the pyramidal cells within the cerebral cortex layer V of the precentral motor area, the premotor area and the postcentral gyrus, then descend into and through the medulla to form the lateral corticospinal tract and the anterior corticospinal tract
Synonyms (1)
"abnormal pyramidal tract morphology" EXACT
Parents (1)
img abnormal nervous system tract morphology MP:0000778
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036315img abnormal nervous system tract morphology MP:0000778
Genes (13)

Species:
human : 13
SpeciesGeneGeneIdGene NameEvidence
HumanALS257679amyotrophic lateral sclerosis 2 (juvenile)
Click here to display 38 evidence detail records.
HumanFEZF255079FEZ family zinc finger 2
Click here to display 38 evidence detail records.
HumanBHLHE2227319basic helix-loop-helix family, member e22
Click here to display 38 evidence detail records.
HumanPNPLA610908patatin-like phospholipase domain containing 6
Click here to display 38 evidence detail records.
HumanNTN19423netrin 1
Click here to display 38 evidence detail records.
HumanUNC5C8633unc-5 homolog C (C. elegans)
Click here to display 38 evidence detail records.
HumanL1CAM3897L1 cell adhesion molecule
Click here to display 38 evidence detail records.
HumanFOXG12290forkhead box G1
Click here to display 38 evidence detail records.
HumanEPHA42043EPH receptor A4
Click here to display 38 evidence detail records.
HumanCELSR31951cadherin, EGF LAG seven-pass G-type receptor 3
Click here to display 38 evidence detail records.
HumanEFNB31949ephrin-B3
Click here to display 38 evidence detail records.
HumanDCC1630deleted in colorectal carcinoma
Click here to display 38 evidence detail records.
HumanCHN11123chimerin 1
Click here to display 38 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002878abnormal corticospinal tract morphology0self