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Details
Link-It Detail - Jax Mouse Phenotype - abnormal dorsal telencephalic commissure morphology
Debug Stats
  • ### Total Build Time: 46 ms 24.178 KB
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  • CONCEPT_GENES gt=18 ms Completed: 18 ms rowSize= 17.350 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.188 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal dorsal telencephalic commissure morphology MP:0008219
Definition (1)
any structural anomaly of the fiber tracts that connect the dorsal region of the two cerebral hemispheres and span the longitudinal fissure, including the corpus callosum and hippocampal commissure
Synonyms (1)
"abnormal dorsal commissure" EXACT
Parents (1)
img abnormal brain commissure morphology MP:0002199
Children (2)
img abnormal hippocampal commissure morphology MP:0008221
img abnormal corpus callosum morphology MP:0000780
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036317img abnormal brain commissure morphology MP:0002199
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036316img abnormal brain commissure morphology MP:0002199
Genes (93)

Species:
human : 93
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCOMMD3-BMI1100532731
INFERRED
HumanDRAXIN374946dorsal inhibitory axon guidance protein
INFERRED
HumanARX170302aristaless related homeobox
INFERRED
HumanLYNX166004Ly6/neurotoxin 1
INFERRED
HumanMARCKSL165108MARCKS-like 1
INFERRED
HumanMARCH764844membrane-associated ring finger (C3HC4) 7, E3 ubiquitin protein ligase
INFERRED
HumanLHX564211LIM homeobox 5
INFERRED
HumanNPAS364067neuronal PAS domain protein 3
INFERRED
HumanVANGL257216VANGL planar cell polarity protein 2
INFERRED
HumanPRDM856978PR domain containing 8
INFERRED
HumanCHD755636chromodomain helicase DNA binding protein 7
INFERRED
HumanFEZF255079FEZ family zinc finger 2
INFERRED
HumanZDHHC1354503zinc finger, DHHC-type containing 13
INFERRED
HumanITSN250618intersectin 2
INFERRED
HumanBHLHE2227319basic helix-loop-helix family, member e22
INFERRED
HumanSLC17A526503solute carrier family 17 (acidic sugar transporter), member 5
INFERRED
HumanCNTNAP226047contactin associated protein-like 2
INFERRED
HumanTSKU25987tsukushi, small leucine rich proteoglycan
INFERRED
HumanNIPBL25836Nipped-B homolog (Drosophila)
INFERRED
HumanSUZ1223512SUZ12 polycomb repressive complex 2 subunit
INFERRED
HumanRPGRIP1L23322RPGRIP1-like
INFERRED
HumanMAPK8IP323162mitogen-activated protein kinase 8 interacting protein 3
img Jax MP, Pubmed Id: 19093031, MOUSE PHENOTYPE ID: MGI:96071
img Jax MP, Pubmed Id: 16715082, MOUSE PHENOTYPE ID: MGI:2176172
img Jax MP, Pubmed Id: 17977657, MOUSE PHENOTYPE ID: MGI:1353598
img Jax MP, Pubmed Id: 17977657, MOUSE PHENOTYPE ID: MGI:1353598
HumanZNF42323090zinc finger protein 423
INFERRED
HumanMYCBP223077MYC binding protein 2, E3 ubiquitin protein ligase
INFERRED
HumanKIF3A11127kinesin family member 3A
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0008219abnormal dorsal telencephalic commissure morphology0self