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 glutamine family amino acid metabolism
Debug Stats
  • ### Total Build Time: 26 ms 16.994 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 228 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 235 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=4 ms Completed: 4 ms rowSize= 457 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.105 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 2.109 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=17 ms Completed: 17 ms rowSize= 11.689 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.047 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of glutamine family amino acid metabolism HP:0010902
Definition (1)
An abnormality of a `glutamine family amino acid metabolic process` (GO:0009064).
Parents (1)
img Abnormality of amino acid metabolism HP:0004337
Children (3)
img Abnormality of proline metabolism HP:0010907
img Abnormality of arginine metabolism HP:0010909
img Abnormality of glutamine metabolism HP:0010903
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of amino acid metabolism HP:0004337
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of amino acid metabolism HP:0004337
Genes (16)

Species:
human : 16
SpeciesGeneGeneIdGene NameEvidence
HumanSLC6A19340024solute carrier family 6 (neutral amino acid transporter), member 19
img HP RolledUp, OMIM ID: 242600
HumanSLC36A2153201solute carrier family 36 (proton/amino acid symporter), member 2
img HP RolledUp, OMIM ID: 242600
HumanPDB494003Paget disease of bone 4
HumanSLC6A2054716solute carrier family 6 (proline IMINO transporter), member 20
img HP RolledUp, OMIM ID: 242600
HumanSLC7A911136solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9
img HP RolledUp, OMIM ID: 220100
HumanSQSTM18878sequestosome 1
HumanTNFRSF11A8792tumor necrosis factor receptor superfamily, member 11a, NFKB activator
img HP RolledUp, OMIM ID: 174810
HumanALDH4A18659aldehyde dehydrogenase 4 family, member A1
img HP RolledUp, OMIM ID: 239510
HumanSLC3A16519solute carrier family 3 (amino acid transporter heavy chain), member 1
img HP RolledUp, OMIM ID: 220100
HumanPRODH5625proline dehydrogenase (oxidase) 1
img HP RolledUp, OMIM ID: 239500
HumanPLOD25352procollagen-lysine, 2-oxoglutarate 5-dioxygenase 2
HumanOTC5009ornithine carbamoyltransferase
HumanTNFRSF11B4982tumor necrosis factor receptor superfamily, member 11b
img HP RolledUp, OMIM ID: 239000
HumanCPS11373carbamoyl-phosphate synthase 1, mitochondrial
img HP RolledUp, OMIM ID: 237300
HumanASS1445argininosuccinate synthase 1
img HP RolledUp, OMIM ID: 215700
HumanASL435argininosuccinate lyase
img HP RolledUp, OMIM ID: 207900
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0010902Abnormality of glutamine family amino acid metabolism0self