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Details
Link-It Detail - Jax Mouse Phenotype - abnormal telencephalon morphology
Debug Stats
  • ### Total Build Time: 169 ms 23.986 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 394 bytes
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  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 181 bytes
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  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 1.575 KB
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  • CONCEPT_GENES gt=159 ms Completed: 159 ms rowSize= 15.376 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.171 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal telencephalon morphology MP:0000787
Definition (1)
any structural anomaly of the paired anteriolateral division of the embryonic prosencephalon plus the lamina terminalis from which the olfactory lobes, cerebral cortex, and subcortical nuclei are derived
Synonyms (1)
"telencephalon dysplasia" EXACT
Parents (1)
img abnormal forebrain morphology MP:0000783
Children (9)
img abnormal telencephalon development MP:0000934
img abnormal lateral ventricle morphology MP:0000823
img telencephalon hypoplasia MP:0000785
img absent Cajal-Retzius cell MP:0000344
img abnormal hippocampus morphology MP:0000807
img abnormal cerebrum morphology MP:0008540
img abnormal septum of telencephalon morphology MP:0012003
img abnormal striatum morphology MP:0004077
img abnormal olfactory lobe morphology MP:0009944
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036316img abnormal forebrain morphology MP:0000783
Genes (573)

Species:
human : 573
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCOMMD3-BMI1100532731
INFERRED
HumanLHX8431707LIM homeobox 8
INFERRED
HumanOR8A1390275olfactory receptor, family 8, subfamily A, member 1
INFERRED
HumanFEZF1389549FEZ family zinc finger 1
INFERRED
HumanINSC387755inscuteable homolog (Drosophila)
INFERRED
HumanDRAXIN374946dorsal inhibitory axon guidance protein
INFERRED
HumanHCN1348980hyperpolarization activated cyclic nucleotide-gated potassium channel 1
INFERRED
HumanLRRTM1347730leucine rich repeat transmembrane neuronal 1
INFERRED
HumanATXN1L342371ataxin 1-like
INFERRED
HumanTFAP2E339488transcription factor AP-2 epsilon (activating enhancer binding protein 2 epsilon)
INFERRED
HumanOR10A4283297olfactory receptor, family 10, subfamily A, member 4
INFERRED
HumanASPM259266asp (abnormal spindle) homolog, microcephaly associated (Drosophila)
INFERRED
HumanEBF3253738early B-cell factor 3
INFERRED
HumanSP8221833Sp8 transcription factor
INFERRED
HumanGSX1219409GS homeobox 1
INFERRED
HumanFBXO45200933F-box protein 45
INFERRED
HumanGSX2170825GS homeobox 2
Click here to display 72 evidence detail records.
HumanARX170302aristaless related homeobox
Click here to display 72 evidence detail records.
HumanOLIG3167826oligodendrocyte transcription factor 3
INFERRED
HumanAK8158067adenylate kinase 8
INFERRED
HumanESCO2157570establishment of sister chromatid cohesion N-acetyltransferase 2
INFERRED
HumanRDH10157506retinol dehydrogenase 10 (all-trans)
INFERRED
HumanGDF7151449growth differentiation factor 7
INFERRED
HumanTTL150465tubulin tyrosine ligase
INFERRED
HumanTRIM71131405tripartite motif containing 71, E3 ubiquitin protein ligase
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000787abnormal telencephalon morphology0self