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Details
Link-It Detail - Human Phenotype - Abnormality of ocular smooth pursuit
Debug Stats
  • ### Total Build Time: 26 ms 29.983 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 211 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 255 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=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 448 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.735 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 3.950 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=16 ms Completed: 16 ms rowSize= 22.230 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.030 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of ocular smooth pursuit HP:0000617
Definition (1)
An `abnormality of eye movement` (HP:0000496) characterized by impaired smooth-pursuit eye movements.
Parents (1)
img Abnormality of eye movement HP:0000496
Children (5)
img Impaired pursuit initiation and maintenance HP:0007668
img Jerky ocular pursuit movements HP:0008003
img Absent smooth pursuit HP:0007179
img Saccadic smooth pursuit HP:0001152
img Impaired smooth pursuit HP:0007772
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of eye movement HP:0000496
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of eye movement HP:0000496
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of eye movement HP:0000496
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of eye movement HP:0000496
Genes (39)

Species:
human : 39
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSCAR7727719spinocerebellar ataxia, autosomal recessive 7
img HP RolledUp, OMIM ID: 609270
HumanATXN8724066ataxin 8
img HP IEA, OMIM ID: 608768
HumanSCA26408221spinocerebellar ataxia 26
img HP RolledUp, OMIM ID: 609306
HumanNYS4317685nystagmus 4, congenital autosomal dominant
img HP RolledUp, OMIM ID: 193003
HumanTSEN54283989TSEN54 tRNA splicing endonuclease subunit
img HP RolledUp, OMIM ID: 277470
HumanSYT14255928synaptotagmin XIV
img HP RolledUp, OMIM ID: 614229
HumanSCA21170545spinocerebellar ataxia 21
img HP RolledUp, OMIM ID: 607454
HumanSCA19140452spinocerebellar ataxia 19
img HP RolledUp, OMIM ID: 607346
HumanCEP4195681centrosomal protein 41kDa
img HP IEA, OMIM ID: 213300
HumanTCTN279867tectonic family member 2
img HP IEA, OMIM ID: 213300
HumanTTC21B79809tetratricopeptide repeat domain 21B
img HP IEA, OMIM ID: 213300
HumanTMEM23179583transmembrane protein 231
img HP IEA, OMIM ID: 213300
HumanC5orf4265250chromosome 5 open reading frame 42
img HP IEA, OMIM ID: 213300
HumanALS257679amyotrophic lateral sclerosis 2 (juvenile)
img HP RolledUp, OMIM ID: 606353
HumanINPP5E56623inositol polyphosphate-5-phosphatase, 72 kDa
img HP IEA, OMIM ID: 213300
HumanPOLR3B55703polymerase (RNA) III (DNA directed) polypeptide B
img HP RolledUp, OMIM ID: 614381
HumanTMEM13851524transmembrane protein 138
img HP IEA, OMIM ID: 213300
HumanTMEM21651259transmembrane protein 216
img HP IEA, OMIM ID: 608091
HumanSACS26278spastic ataxia of Charlevoix-Saguenay (sacsin)
img HP IEA, OMIM ID: 270550
HumanTCTN326123tectonic family member 3
img HP IEA, OMIM ID: 213300
HumanPLEKHG425894pleckstrin homology domain containing, family G (with RhoGef domain) member 4
img HP IEA, OMIM ID: 600223
HumanSETX23064senataxin
img HP RolledUp, OMIM ID: 606002
HumanNOP5610528NOP56 ribonucleoprotein
img HP RolledUp, OMIM ID: 614153
HumanPLA2G68398phospholipase A2, group VI (cytosolic, calcium-independent)
img HP RolledUp, OMIM ID: 610217
HumanTBP6908TATA box binding protein
img HP RolledUp, OMIM ID: 607136
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000617Abnormality of ocular smooth pursuit0self