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Details
Link-It Detail - Jax Mouse Phenotype - abnormal brain morphology
Debug Stats
  • ### Total Build Time: 3,478 ms 27.772 KB
  • CONCEPT_NAME gt=3 ms Completed: 2 ms rowSize= 378 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_GENES gt=3,456 ms Completed: 3.456 Seconds rowSize= 15.468 KB
  • CONCEPT_XREFS gt=7 ms Completed: 7 ms rowSize= 1.163 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal brain morphology MP:0002152
Definition (1)
any structural anomaly of the brain, one of the two components of the central nervous system and the center of thought and emotion; controls coordination, bodily activities and the interpretation of information from the senses (sight, hearing, smell, etc.)
Synonyms (1)
"central nervous system: brain dysmorphology" EXACT
Parents (1)
img abnormal nervous system morphology MP:0003632
Children (17)
img abnormal brain size MP:0000771
img abnormal brain white matter morphology MP:0008026
img abnormal midbrain morphology MP:0000897
img abnormal brain interneuron morphology MP:0004101
img abnormal brain iron level MP:0008811
img abnormal hindbrain morphology MP:0000841
img abnormal brain copper level MP:0011213
img abnormal brain development MP:0000913
img neurofibrillary tangles MP:0003214
img abnormal postnatal subventricular zone morphology MP:0004275
img brain vacuoles MP:0008025
img abnormal forebrain morphology MP:0000783
img abnormal brain ventricle/choroid plexus morphology MP:0002200
img tau protein deposits MP:0004250
img abnormal brainstem morphology MP:0005277
img cerebral amyloid angiopathy MP:0004254
img abnormal brain vasculature morphology MP:0004950
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036314img abnormal nervous system morphology MP:0003632
Genes (1217)

Species:
human : 1217
Page Size
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SpeciesGeneGeneIdGene NameEvidence
HumanCOMMD3-BMI1100532731
Click here to display 282 evidence detail records.
HumanOCLN100506658occludin
INFERRED
HumanSKOR2652991SKI family transcriptional corepressor 2
INFERRED
HumanCBLN3643866cerebellin 3 precursor
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
HumanSHISA2387914shisa family member 2
INFERRED
HumanINSC387755inscuteable homolog (Drosophila)
INFERRED
HumanNHLRC1378884NHL repeat containing 1
INFERRED
HumanDRAXIN374946dorsal inhibitory axon guidance protein
INFERRED
HumanKIF7374654kinesin family member 7
INFERRED
HumanHCN1348980hyperpolarization activated cyclic nucleotide-gated potassium channel 1
INFERRED
HumanLRRTM1347730leucine rich repeat transmembrane neuronal 1
INFERRED
HumanSOWAHB345079sosondowah ankyrin repeat domain family member B
INFERRED
HumanATXN1L342371ataxin 1-like
INFERRED
HumanHMX3340784H6 family homeobox 3
INFERRED
HumanTFAP2E339488transcription factor AP-2 epsilon (activating enhancer binding protein 2 epsilon)
INFERRED
HumanLIN9286826lin-9 homolog (C. elegans)
INFERRED
HumanSUMF1285362sulfatase modifying factor 1
INFERRED
HumanOR10A4283297olfactory receptor, family 10, subfamily A, member 4
INFERRED
HumanASPM259266asp (abnormal spindle) homolog, microcephaly associated (Drosophila)
INFERRED
HumanPTF1A256297pancreas specific transcription factor, 1a
INFERRED
HumanEBF3253738early B-cell factor 3
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002152abnormal brain morphology0self