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Details
Link-It Detail - Human Phenotype - Abnormality of saccadic eye movements
Debug Stats
  • ### Total Build Time: 20 ms 30.767 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 212 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 261 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=3 ms Completed: 3 ms rowSize= 448 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 2.654 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=12 ms Completed: 12 ms rowSize= 22.087 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.031 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of saccadic eye movements HP:0000570
Definition (1)
An `abnormality of eye movement` (HP:0000496) characterized by impairment of fast (saccadic) eye movements.
Parents (1)
img Abnormality of eye movement HP:0000496
Children (8)
img Slow saccadic eye movements HP:0000514
img Hypometric saccades HP:0000571
img Impaired saccades HP:0000604
img Slowed horizontal saccades HP:0007885
img Saccadic slow pursuit HP:0000530
img Dysmetric saccades HP:0000641
img Abnormal visual pursuit HP:0008029
img Hypermetric saccades HP:0007338
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
HumanSCA30100359393spinocerebellar ataxia 30
img HP RolledUp, OMIM ID: 613371
HumanSCAR7727719spinocerebellar ataxia, autosomal recessive 7
img HP RolledUp, OMIM ID: 609270
HumanATXN8724066ataxin 8
img HP RolledUp, OMIM ID: 608768
HumanSCA26408221spinocerebellar ataxia 26
img HP RolledUp, OMIM ID: 609306
HumanSCA20407973spinocerebellar ataxia 20
img HP RolledUp, OMIM ID: 608687
HumanTSEN54283989TSEN54 tRNA splicing endonuclease subunit
img HP RolledUp, OMIM ID: 277470
HumanSCASI260415spinocerebellar ataxia with saccadic intrusions
img HP RolledUp, OMIM ID: 607317
HumanSCA21170545spinocerebellar ataxia 21
img HP RolledUp, OMIM ID: 607454
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
HumanGJC257165gap junction protein, gamma 2, 47kDa
img HP RolledUp, OMIM ID: 613206
HumanINPP5E56623inositol polyphosphate-5-phosphatase, 72 kDa
img HP IEA, OMIM ID: 213300
HumanANO1055129anoctamin 10
img HP RolledUp, OMIM ID: 613728
HumanAPTX54840aprataxin
img HP RolledUp, OMIM ID: 208920
HumanTMEM13851524transmembrane protein 138
img HP IEA, OMIM ID: 213300
HumanTMEM21651259transmembrane protein 216
img HP IEA, OMIM ID: 608091
HumanTCTN326123tectonic family member 3
img HP IEA, OMIM ID: 213300
HumanFBXO725793F-box protein 7
img HP RolledUp, OMIM ID: 260300
HumanPIK3R523533phosphoinositide-3-kinase, regulatory subunit 5
img HP RolledUp, OMIM ID: 615217
HumanATP13A223400ATPase type 13A2
img HP RolledUp, OMIM ID: 606693
HumanAFG3L210939AFG3 ATPase family member 3-like 2 (S. cerevisiae)
img HP RolledUp, OMIM ID: 610246
HumanNOP5610528NOP56 ribonucleoprotein
img HP RolledUp, OMIM ID: 614153
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000570Abnormality of saccadic eye movements0self