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Details
Link-It Detail - Jax Mouse Phenotype - abnormal brain development
Debug Stats
  • ### Total Build Time: 1,110 ms 28.085 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 380 bytes
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  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 2.918 KB
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  • CONCEPT_GENES gt=1,107 ms Completed: 1.107 Seconds rowSize= 15.544 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.164 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal brain development MP:0000913
Definition (1)
aberrant or incomplete differentiation of the brain
Synonyms (1)
"brain development abnormalities" EXACT
Parents (2)
img abnormal brain morphology MP:0002152
img abnormal nervous system development MP:0003861
Children (14)
img abnormal cervical flexure morphology MP:0010744
img exencephaly MP:0000914
img hydroencephaly MP:0001891
img abnormal primordial meninx morphology MP:0009726
img delayed brain development MP:0001889
img increased oligodendrocyte progenitor number MP:0010892
img abnormal olfactory bulb development MP:0002739
img abnormal isthmic organizer morphology MP:0006174
img abnormal embryonic neuroepithelial layer differentiation MP:0000786
img holoprosencephaly MP:0005157
img decreased oligodendrocyte progenitor number MP:0000954
img abnormal forebrain development MP:0003232
img abnormal midbrain development MP:0003864
img abnormal hindbrain development MP:0006108
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036315img abnormal brain morphology MP:0002152
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036315img abnormal nervous system development MP:0003861
Genes (562)

Species:
human : 562
Page Size
Current 25
  Page 1 of 23
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSKOR2652991SKI family transcriptional corepressor 2
INFERRED
HumanLHX8431707LIM homeobox 8
INFERRED
HumanOR8A1390275olfactory receptor, family 8, subfamily A, member 1
INFERRED
HumanFEZF1389549FEZ family zinc finger 1
INFERRED
HumanFAM212A389119family with sequence similarity 212, member A
INFERRED
HumanINSC387755inscuteable homolog (Drosophila)
Click here to display 157 evidence detail records.
HumanKIF7374654kinesin family member 7
INFERRED
HumanHCN1348980hyperpolarization activated cyclic nucleotide-gated potassium channel 1
INFERRED
HumanSOWAHB345079sosondowah ankyrin repeat domain family member B
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
HumanPTF1A256297pancreas specific transcription factor, 1a
INFERRED
HumanIPMK253430inositol polyphosphate multikinase
Click here to display 157 evidence detail records.
HumanSP8221833Sp8 transcription factor
INFERRED
HumanTBC1D32221322TBC1 domain family, member 32
INFERRED
HumanTBATA219793thymus, brain and testes associated
INFERRED
HumanFBXO45200933F-box protein 45
INFERRED
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
INFERRED
HumanGSX2170825GS homeobox 2
Click here to display 157 evidence detail records.
HumanARX170302aristaless related homeobox
INFERRED
HumanBMPER168667BMP binding endothelial regulator
INFERRED
HumanOLIG3167826oligodendrocyte transcription factor 3
INFERRED
HumanAK8158067adenylate kinase 8
INFERRED
HumanESCO2157570establishment of sister chromatid cohesion N-acetyltransferase 2
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000913abnormal brain development0self