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Details
Link-It Detail - Jax Mouse Phenotype - abnormal corpus callosum morphology
Debug Stats
  • ### Total Build Time: 173 ms 25.070 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 398 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= 183 bytes
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  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 4.300 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=164 ms Completed: 164 ms rowSize= 16.423 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.173 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal corpus callosum morphology MP:0000780
Definition (1)
any structural anomaly of a thick bundle of nerve fibers comprising a commissural plate connecting the two cerebral hemispheres; it consists of contralateral axon projections that provides communications between the right and left cerebral hemispheres
Synonyms (1)
"corpus callosum dysplasia" EXACT
Parents (2)
img abnormal cerebrum morphology MP:0008540
img abnormal dorsal telencephalic commissure morphology MP:0008219
Children (2)
img absent corpus callosum MP:0002196
img decreased corpus callosum size MP:0000781
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036318img abnormal cerebrum morphology MP:0008540
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036318img abnormal dorsal telencephalic commissure morphology MP:0008219
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036317img abnormal dorsal telencephalic commissure morphology MP:0008219
Genes (90)

Species:
human : 90
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SpeciesGeneGeneIdGene NameEvidence
HumanCOMMD3-BMI1100532731
Click here to display 78 evidence detail records.
HumanDRAXIN374946dorsal inhibitory axon guidance protein
INFERRED
HumanARX170302aristaless related homeobox
Click here to display 78 evidence detail records.
HumanLYNX166004Ly6/neurotoxin 1
Click here to display 78 evidence detail records.
HumanMARCKSL165108MARCKS-like 1
INFERRED
HumanMARCH764844membrane-associated ring finger (C3HC4) 7, E3 ubiquitin protein ligase
Click here to display 78 evidence detail records.
HumanNPAS364067neuronal PAS domain protein 3
Click here to display 78 evidence detail records.
HumanVANGL257216VANGL planar cell polarity protein 2
Click here to display 78 evidence detail records.
HumanPRDM856978PR domain containing 8
INFERRED
HumanCHD755636chromodomain helicase DNA binding protein 7
Click here to display 78 evidence detail records.
HumanFEZF255079FEZ family zinc finger 2
INFERRED
HumanZDHHC1354503zinc finger, DHHC-type containing 13
Click here to display 78 evidence detail records.
HumanITSN250618intersectin 2
Click here to display 78 evidence detail records.
HumanBHLHE2227319basic helix-loop-helix family, member e22
INFERRED
HumanSLC17A526503solute carrier family 17 (acidic sugar transporter), member 5
Click here to display 78 evidence detail records.
HumanCNTNAP226047contactin associated protein-like 2
Click here to display 78 evidence detail records.
HumanTSKU25987tsukushi, small leucine rich proteoglycan
Click here to display 78 evidence detail records.
HumanNIPBL25836Nipped-B homolog (Drosophila)
INFERRED
HumanSUZ1223512SUZ12 polycomb repressive complex 2 subunit
INFERRED
HumanRPGRIP1L23322RPGRIP1-like
INFERRED
HumanMAPK8IP323162mitogen-activated protein kinase 8 interacting protein 3
Click here to display 78 evidence detail records.
HumanZNF42323090zinc finger protein 423
Click here to display 78 evidence detail records.
HumanMYCBP223077MYC binding protein 2, E3 ubiquitin protein ligase
Click here to display 78 evidence detail records.
HumanKIF3A11127kinesin family member 3A
INFERRED
HumanVAX111023ventral anterior homeobox 1
Click here to display 78 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000780abnormal corpus callosum morphology0self