Logo arc image image
GATACA
  • Pin/Unpin Search
  • Pin/Unpin Details
Status:
Global Actions
Concepts: 0 (0)   Selected: 0 (0
Clear All Selections
 
Search
Text Search Results
Text Search Query:
none
Text Search Options:
none

Guided Help

Text Search Results
GraphTree Minimize or Maximize this Category
 Disease: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Anatomy: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Gene: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Jax Mouse Phenotype: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Human Phenotype: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Biological Processes: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Cellular Component: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Molecular Function: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Pathway: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Drug: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Genomic Expression Atlas --
      Microarray Datasets: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 PubMed: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 CoExpression Atlas: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 CoExpression: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Interactions: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Details
Link-It Detail - Human Phenotype - Abnormality of coordination
Debug Stats
  • ### Total Build Time: 42 ms 24.196 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 202 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=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= 458 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.357 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.173 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=34 ms Completed: 34 ms rowSize= 19.855 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.021 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of coordination HP:0011443
Parents (1)
img Abnormality of central motor function HP:0011442
Children (4)
img Slurred speech HP:0001350
img Ataxia HP:0001251
img Incoordination HP:0002311
img Poor motor coordination HP:0002275
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of central motor function HP:0011442
Genes (487)

Species:
human : 487
Page Size
Current 25
  Page 1 of 20
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanHMSN5101059903Hereditary motor and sensory neuropathy V
HumanSPG46100861438spastic paraplegia 46 (autosomal recessive)
img HP RolledUp, OMIM ID: 614409
HumanSCAR12100820764Spinocerebellar ataxia, autosomal recessive 12
img HP RolledUp, OMIM ID: 614322
HumanMRXSCS100820761Mental retardation, X-linked, syndromic, Chudley-Schwartz type
img HP RolledUp, OMIM ID: 300861
HumanDEL2Q23.1100820633
img HP RolledUp, OMIM ID: 156200
HumanSCA34100750330spinocerebellar ataxia 34
img HP RolledUp, OMIM ID: 133190
HumanSPAX3100379201Ataxia, spastic, 3, autosomal recessive
HumanSCA31100312950spinocerebellar ataxia 31
img HP RolledUp, OMIM ID: 117210
HumanHTGH100302716Hypertrichosis terminalis, generalized, with or without gingival hyperplasia
img HP RolledUp, OMIM ID: 135400
HumanDEL18Q100216483Chromosome 18q deletion syndrome
HumanEA7100188859Episodic ataxia, type 7
HumanMICRODEL3Q29100188788Chromosome 3q29 microdeletion syndrome
HumanSCAX5100188768Spinocerebellar ataxia, X-linked 5
img HP RolledUp, OMIM ID: 300703
HumanCD24100133941CD24 molecule
img HP RolledUp, OMIM ID: 126200
HumanSAX2100126095spastic ataxia 2 (autosomal recessive)
HumanSCA29100038747spinocerebellar ataxia 29
img HP RolledUp, OMIM ID: 117360
HumanSNORD116-1100033413
img HP RolledUp, OMIM ID: 176270
HumanPWRN1791114Prader-Willi region non-protein coding RNA 1
img HP RolledUp, OMIM ID: 176270
HumanCHMRQ780925Cerebellar hypoplasia, mental retardation, and quadrupedal locomotion
HumanMPD3780920Myopathy, distal 3
HumanEA3780905Episodic ataxia, type 3
HumanSCAR7727719spinocerebellar ataxia, autosomal recessive 7
img HP RolledUp, OMIM ID: 609270
HumanSCAX4727716spinocerebellar ataxia, X-linked 4
img HP RolledUp, OMIM ID: 301840
HumanSCAX3727715spinocerebellar ataxia, X-linked 3
img HP RolledUp, OMIM ID: 301790
HumanSCAX2727714spinocerebellar ataxia, X-linked 2
img HP RolledUp, OMIM ID: 302600
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011443Abnormality of coordination0self