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Details
Link-It Detail - Jax Mouse Phenotype - abnormal amino acid level
Debug Stats
  • ### Total Build Time: 226 ms 21.303 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 378 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 272 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=5 ms Completed: 5 ms rowSize= 575 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 1.487 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.574 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=204 ms Completed: 204 ms rowSize= 15.737 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.163 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal amino acid level MP:0005332
Definition (1)
any anomaly in the amount of a carboxylic acid containing one or more amino groups (-NH2) and a carboxyl (-COOH) group
Parents (1)
img abnormal homeostasis MP:0001764
Children (3)
img abnormal circulating amino acid level MP:0005311
img abnormal creatine level MP:0010060
img abnormal urine amino acid level MP:0011468
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053764img abnormal homeostasis MP:0001764
Genes (183)

Species:
human : 183
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED
HumanEIF2AK4440275eukaryotic translation initiation factor 2 alpha kinase 4
INFERRED
HumanSLC6A18348932solute carrier family 6 (neutral amino acid transporter), member 18
INFERRED
HumanSLC6A19340024solute carrier family 6 (neutral amino acid transporter), member 19
INFERRED
HumanNEK8284086NIMA-related kinase 8
INFERRED
HumanAQP11282679aquaporin 11
INFERRED
HumanCYS1192668cystin 1
INFERRED
HumanNAGS162417N-acetylglutamate synthase
INFERRED
HumanPPM1K152926protein phosphatase, Mg2+/Mn2+ dependent, 1K
INFERRED
HumanSLC46A1113235solute carrier family 46 (folate transporter), member 1
Click here to display 58 evidence detail records.
HumanGLIS284662GLIS family zinc finger 2
INFERRED
HumanWDR8384292WD repeat domain 83
INFERRED
HumanQTRT181890queuine tRNA-ribosyltransferase 1
INFERRED
HumanUNC93B181622unc-93 homolog B1 (C. elegans)
INFERRED
HumanCOL18A180781collagen, type XVIII, alpha 1
INFERRED
HumanSRR63826serine racemase
Click here to display 58 evidence detail records.
HumanSLC4A557835solute carrier family 4 (sodium bicarbonate cotransporter), member 5
INFERRED
HumanTMEM2757393transmembrane protein 27
Click here to display 58 evidence detail records.
HumanC1GALT156913core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1
INFERRED
HumanSLC2A956606solute carrier family 2 (facilitated glucose transporter), member 9
INFERRED
HumanSLC7A1056301solute carrier family 7 (neutral amino acid transporter light chain, asc system), member 10
Click here to display 58 evidence detail records.
HumanLGR455366leucine-rich repeat containing G protein-coupled receptor 4
INFERRED
HumanSLC47A155244solute carrier family 47 (multidrug and toxin extrusion), member 1
INFERRED
HumanPANK153354pantothenate kinase 1
Click here to display 58 evidence detail records.
HumanATP8A251761ATPase, aminophospholipid transporter, class I, type 8A, member 2
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0005332abnormal amino acid level0self