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Details
Link-It Detail - Human Phenotype - Abnormal thickness of corpus callosum
Debug Stats
  • ### Total Build Time: 82 ms 30.088 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 212 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=11 ms Completed: 11 ms rowSize= 455 bytes
  • CONCEPT_CHILDREN gt=12 ms Completed: 12 ms rowSize= 767 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=28 ms Completed: 28 ms rowSize= 4.916 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=26 ms Completed: 26 ms rowSize= 22.596 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.031 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal thickness of corpus callosum HP:0200010
Parents (1)
img Abnormality of the corpus callosum HP:0001273
Children (2)
img Thin corpus callosum HP:0002319
img Thick corpus callosum HP:0007074
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the corpus callosum HP:0001273
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the corpus callosum HP:0001273
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the corpus callosum HP:0001273
img All HP:0000001img Phenotypic abnormality HP:000011810img Abnormality of the corpus callosum HP:0001273
img All HP:0000001img Phenotypic abnormality HP:000011811img Abnormality of the corpus callosum HP:0001273
Genes (49)

Species:
human : 49
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSPG46100861438spastic paraplegia 46 (autosomal recessive)
img HP RolledUp, OMIM ID: 614409
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP RolledUp, OMIM ID: 607872
HumanSPG32724107spastic paraplegia 32 (autosomal recessive)
img HP RolledUp, OMIM ID: 611252
HumanTUBB2B347733tubulin, beta 2B class IIb
img HP RolledUp, OMIM ID: 610031
HumanWDR62284403WD repeat domain 62
img HP RolledUp, OMIM ID: 604317
HumanKCTD7154881potassium channel tetramerization domain containing 7
img HP RolledUp, OMIM ID: 611726
HumanEARS2124454glutamyl-tRNA synthetase 2, mitochondrial
img HP RolledUp, OMIM ID: 614924
HumanCYP2U1113612cytochrome P450, family 2, subfamily U, polypeptide 1
img HP RolledUp, OMIM ID: 615030
HumanTRAPPC983696trafficking protein particle complex 9
img HP RolledUp, OMIM ID: 613192
HumanSPG1180208spastic paraplegia 11 (autosomal recessive)
img HP RolledUp, OMIM ID: 604360
HumanSNIP179753Smad nuclear interacting protein 1
img HP RolledUp, OMIM ID: 614501
HumanFA2H79152fatty acid 2-hydroxylase
img HP RolledUp, OMIM ID: 612319
HumanGBA257704glucosidase, beta (bile acid) 2
img HP RolledUp, OMIM ID: 614409
HumanKCNT157582potassium channel, subfamily T, member 1
img HP RolledUp, OMIM ID: 614959
HumanGJC257165gap junction protein, gamma 2, 47kDa
img HP RolledUp, OMIM ID: 613206
HumanPOLR3B55703polymerase (RNA) III (DNA directed) polypeptide B
img HP RolledUp, OMIM ID: 607694
HumanRMND155005required for meiotic nuclear division 1 homolog (S. cerevisiae)
img HP RolledUp, OMIM ID: 614922
HumanTREM254209triggering receptor expressed on myeloid cells 2
img HP RolledUp, OMIM ID: 221770
HumanMBTPS251360membrane-bound transcription factor peptidase, site 2
img HP RolledUp, OMIM ID: 308205
img HP RolledUp, OMIM ID: 300404
HumanIER3IP151124immediate early response 3 interacting protein 1
img HP RolledUp, OMIM ID: 614231
HumanSEPSECS51091Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase
img HP RolledUp, OMIM ID: 613811
HumanATL151062atlastin GTPase 1
img HP RolledUp, OMIM ID: 182600
HumanSETBP126040SET binding protein 1
img HP RolledUp, OMIM ID: 269150
HumanCOG425839component of oligomeric golgi complex 4
img HP RolledUp, OMIM ID: 613489
HumanZFYVE2623503zinc finger, FYVE domain containing 26
img HP RolledUp, OMIM ID: 270700
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0200010Abnormal thickness of corpus callosum0self