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 - Disease - Xeroderma pigmentosum, group G
Debug Stats
  • ### Total Build Time: 44 ms 19.498 KB
  • CONCEPT_NAME gt=8 ms Completed: 8 ms rowSize= 358 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=0 Completed: 0 ms rowSize= 7 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=29 ms Completed: 29 ms rowSize= 9.160 KB
  • CONCEPT_GENES gt=5 ms Completed: 5 ms rowSize= 8.754 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.164 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Xeroderma pigmentosum, group G C0268141
Relationships (17)

Relation Types:
diso_​to_​anat : 2
diso_​to_​diso : 13
diso_​to_​gene : 2


Relationships:
expanded_​form_​of : 1
gene_​associated_​with_​disease : 2
is_​associated_​anatomic_​site_​of : 1
is_​finding_​of_​disease : 1
is_​primary_​anatomic_​site_​of_​disease : 1
manifestation_​of : 6
may_​be_​associated_​disease_​of_​disease : 3
related_​to : 2
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANATis_associated_anatomic_site_ofimg Integumentary System C0037267
DISO_to_ANATis_primary_anatomic_site_of_diseaseimg Skin C1123023
DISO_to_DISOmanifestation_ofimg Abnormal sensitivity to UVB wavelengths by radiation monochromator skin testing C3279492
DISO_to_DISOmay_be_associated_disease_of_diseaseimg Basal cell carcinoma C0007117
DISO_to_DISOrelated_toimg CEREBROOCULOFACIOSKELETAL SYNDROME 3 C1851443
DISO_to_DISOmanifestation_ofimg Caused by mutation in the excision-repair, complementing defective, in Chinese hamster, number 5 gene (ERCC5, 133530.0001) C3279494
DISO_to_DISOis_finding_of_diseaseimg Cutaneous Involvement C1511567
DISO_to_DISOmay_be_associated_disease_of_diseaseimg Cutaneous Melanoma C0151779
DISO_to_DISOmanifestation_ofimg Defective DNA repair after ultraviolet radiation damage C1968564
DISO_to_DISOmanifestation_ofimg Mild cutaneous changes C3279491
DISO_to_DISOmanifestation_ofimg No UV-induced skin tumors C3279493
DISO_to_DISOmanifestation_ofimg Normal physical and neurologic development C3279495
DISO_to_DISOmay_be_associated_disease_of_diseaseimg Squamous cell carcinoma of skin C0553723
DISO_to_DISOrelated_toimg XERODERMA PIGMENTOSUM, TYPE G/COCKAYNE SYNDROME C1968561
DISO_to_DISOexpanded_form_ofimg Xeroderma pigmentosum, group G C0268141
DISO_to_GENEgene_associated_with_diseaseimg ERCC5 gene C1333359
DISO_to_GENEgene_associated_with_diseaseimg ERCC5 wt Allele C1705470
Genes (7)

Species:
human : 6
mouse : 1
SpeciesGeneGeneIdGene NameEvidence
MouseERCC52073excision repair cross-complementing rodent repair deficiency, complementation group 5
img NCI, Score=801, Pubmed Id: 12893972, UMLKSK CUI: C0268141
HumanXRCC37517X-ray repair complementing defective repair in Chinese hamster cells 3
img NCI, Score=801, Pubmed Id: 10409751, UMLKSK CUI: C0268141
HumanSTAT16772signal transducer and activator of transcription 1, 91kDa
img NCI, Score=801, Pubmed Id: 9828143, UMLKSK CUI: C0268141
HumanGLS2744glutaminase
img NCI, Score=801, Pubmed Id: 9828143, UMLKSK CUI: C0268141
HumanERCC52073excision repair cross-complementing rodent repair deficiency, complementation group 5
Click here to display 19 evidence detail records.
HumanERCC42072excision repair cross-complementing rodent repair deficiency, complementation group 4
img NCI, Score=801, Pubmed Id: 10409751, UMLKSK CUI: C0268141
HumanERCC22068excision repair cross-complementing rodent repair deficiency, complementation group 2
img NCI, Score=801, Pubmed Id: 12208738, UMLKSK CUI: C0268141
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0268141Xeroderma pigmentosum, group G0self