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Details
Link-It Detail - Human Phenotype - Abnormality of lysine metabolism
Debug Stats
  • ### Total Build Time: 15 ms 9.556 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 207 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=2 ms Completed: 2 ms rowSize= 474 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 754 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 2.143 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 4.841 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.026 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of lysine metabolism HP:0010908
Parents (1)
img Abnormality of aspartate family amino acid metabolism HP:0010899
Children (2)
img Hyperlysinemia HP:0002161
img Hyperlysinuria HP:0003297
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of aspartate family amino acid metabolism HP:0010899
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of aspartate family amino acid metabolism HP:0010899
Genes (5)

Species:
human : 5
SpeciesGeneGeneIdGene NameEvidence
HumanSLC7A911136solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9
img HP RolledUp, OMIM ID: 220100
HumanAASS10157aminoadipate-semialdehyde synthase
img HP RolledUp, OMIM ID: 238700
img HP RolledUp, OMIM ID: 268700
HumanSLC3A16519solute carrier family 3 (amino acid transporter heavy chain), member 1
img HP RolledUp, OMIM ID: 220100
HumanDECR116662,4-dienoyl CoA reductase 1, mitochondrial
img HP RolledUp, OMIM ID: 222745
HumanARG1383arginase 1
img HP RolledUp, OMIM ID: 207800
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0010908Abnormality of lysine metabolism0self