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Details
Link-It Detail - Disease - Delay in motor development
Debug Stats
  • ### Total Build Time: 44 ms 25.597 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 350 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=2 ms Completed: 2 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=35 ms Completed: 35 ms rowSize= 23.921 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.160 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Delay in motor development C1864913
Genes (59)

Species:
human : 59
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanFGD4121512FYVE, RhoGEF and PH domain containing 4
img OMIM, Score=1000, UMLKSK CUI: C1864913
HumanGFM185476G elongation factor, mitochondrial 1
img OMIM, Score=1000, UMLKSK CUI: C1864913
HumanFAM126A84668family with sequence similarity 126, member A
img OMIM, Score=1000, UMLKSK CUI: C1864913
HumanSH3TC279628SH3 domain and tetratricopeptide repeats 2
img OMIM, Score=1000, UMLKSK CUI: C1864913
HumanPRX57716periaxin
img OMIM, Score=1000, UMLKSK CUI: C1864913
HumanALS257679amyotrophic lateral sclerosis 2 (juvenile)
img OMIM, Score=1000, UMLKSK CUI: C1864913
HumanSEPN157190selenoprotein N, 1
img OMIM, Score=1000, UMLKSK CUI: C1864913
HumanPDSS257107prenyl (decaprenyl) diphosphate synthase, subunit 2
img OMIM, Score=1000, UMLKSK CUI: C1864913
HumanADCK356997aarF domain containing kinase 3
img OMIM, Score=1000, UMLKSK CUI: C1864913
HumanMBD555777methyl-CpG binding domain protein 5
img OMIM, Score=1000, UMLKSK CUI: C1864913
HumanAPTX54840aprataxin
img OMIM, Score=1000, UMLKSK CUI: C1864913
HumanAHI154806Abelson helper integration site 1
img OMIM, Score=1000, UMLKSK CUI: C1864913
HumanGDAP154332ganglioside induced differentiation associated protein 1
img OMIM, Score=1000, UMLKSK CUI: C1864913
HumanATL151062atlastin GTPase 1
img OMIM, Score=1000, UMLKSK CUI: C1864913
HumanCOQ227235coenzyme Q2 4-hydroxybenzoate polyprenyltransferase
img OMIM, Score=1000, UMLKSK CUI: C1864913
HumanPDSS123590prenyl (decaprenyl) diphosphate synthase, subunit 1
img OMIM, Score=1000, UMLKSK CUI: C1864913
HumanPOMT110585protein-O-mannosyltransferase 1
img OMIM, Score=909, UMLKSK CUI: C1864913
HumanATP6AP210159ATPase, H+ transporting, lysosomal accessory protein 2
img OMIM, Score=1000, UMLKSK CUI: C1864913
HumanHUWE110075HECT, UBA and WWE domain containing 1, E3 ubiquitin protein ligase
img OMIM, Score=1000, UMLKSK CUI: C1864913
HumanZEB29839zinc finger E-box binding homeobox 2
img OMIM, Score=1000, UMLKSK CUI: C1864913
HumanLARGE9215like-glycosyltransferase
img OMIM, Score=1000, UMLKSK CUI: C1864913
HumanCTDP19150CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) phosphatase, subunit 1
img OMIM, Score=1000, UMLKSK CUI: C1864913
HumanMTMR28898myotubularin related protein 2
img OMIM, Score=1000, UMLKSK CUI: C1864913
HumanALDH5A17915aldehyde dehydrogenase 5 family, member A1
img OMIM, Score=1000, UMLKSK CUI: C1864913
HumanTUBA1A7846tubulin, alpha 1a
img OMIM, Score=1000, UMLKSK CUI: C1864913
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C1864913Delay in motor development0self