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Details
Link-It Detail - Jax Mouse Phenotype - abnormal urine amino acid level
Debug Stats
  • ### Total Build Time: 119 ms 33.501 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 390 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 285 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=51 ms Completed: 51 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= 1.019 KB
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.014 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 4.270 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=46 ms Completed: 46 ms rowSize= 25.227 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.169 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal urine amino acid level MP:0011468
Definition (1)
any anomaly in the amount in the urine of a carboxylic acid containing one or more amino groups (-NH2) and a carboxyl (-COOH) group
Parents (2)
img abnormal amino acid level MP:0005332
img abnormal urine homeostasis MP:0009643
Children (2)
img abnormal urine creatinine level MP:0011469
img aminoaciduria MP:0003311
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053765img abnormal amino acid level MP:0005332
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053765img abnormal urine homeostasis MP:0009643
img mammalian phenotype MP:0000001img renal/urinary system phenotype MP:00053675img abnormal urine homeostasis MP:0009643
Genes (35)

Species:
human : 35
Page Size
Current 25
  Page 1 of 2
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSLC6A18348932solute carrier family 6 (neutral amino acid transporter), member 18
INFERRED
HumanSLC6A19340024solute carrier family 6 (neutral amino acid transporter), member 19
INFERRED
HumanTMEM2757393transmembrane protein 27
INFERRED
HumanSLC7A911136solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9
INFERRED
HumanAKR1A110327aldo-keto reductase family 1, member A1 (aldehyde reductase)
INFERRED
HumanSLC23A19963solute carrier family 23 (ascorbic acid transporter), member 1
INFERRED
HumanATG59474autophagy related 5
INFERRED
HumanSLC7A79056solute carrier family 7 (amino acid transporter light chain, y+L system), member 7
INFERRED
HumanSLC14A28170solute carrier family 14 (urea transporter), member 2
INFERRED
HumanUPK27379uroplakin 2
INFERRED
HumanUMOD7369uromodulin
INFERRED
HumanHNF1A6927HNF1 homeobox A
INFERRED
HumanSLC22A56584solute carrier family 22 (organic cation/carnitine transporter), member 5
INFERRED
HumanSLC14A16563solute carrier family 14 (urea transporter), member 1
INFERRED
HumanSLC12A16557solute carrier family 12 (sodium/potassium/chloride transporter), member 1
INFERRED
HumanSLC5A26524solute carrier family 5 (sodium/glucose cotransporter), member 2
INFERRED
HumanSLC3A16519solute carrier family 3 (amino acid transporter heavy chain), member 1
img Jax MP, Pubmed Id: 9233792, MOUSE PHENOTYPE ID: MGI:105083
img Jax MP, Pubmed Id: 17767905, MOUSE PHENOTYPE ID: MGI:1276534
img Jax MP, Pubmed Id: 23026748, MOUSE PHENOTYPE ID: MGI:1914342
img Jax MP, Pubmed Id: 12923163, MOUSE PHENOTYPE ID: MGI:1195264
img Jax MP, Pubmed Id: 15028668, MOUSE PHENOTYPE ID: MGI:1098221
HumanSLC1A16505solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1
img Jax MP, Pubmed Id: 9233792, MOUSE PHENOTYPE ID: MGI:105083
img Jax MP, Pubmed Id: 12923163, MOUSE PHENOTYPE ID: MGI:1195264
img Jax MP, Pubmed Id: 23026748, MOUSE PHENOTYPE ID: MGI:1914342
img Jax MP, Pubmed Id: 17767905, MOUSE PHENOTYPE ID: MGI:1276534
img Jax MP, Pubmed Id: 15028668, MOUSE PHENOTYPE ID: MGI:1098221
HumanSCTR6344secretin receptor
INFERRED
HumanINPP5B3633inositol polyphosphate-5-phosphatase, 75kDa
INFERRED
HumanHSD11B23291hydroxysteroid (11-beta) dehydrogenase 2
INFERRED
HumanHGD3081homogentisate 1,2-dioxygenase
INFERRED
HumanHAL3034histidine ammonia-lyase
INFERRED
HumanGCDH2639glutaryl-CoA dehydrogenase
INFERRED
HumanGATM2628glycine amidinotransferase (L-arginine:glycine amidinotransferase)
img Jax MP, Pubmed Id: 15028668, MOUSE PHENOTYPE ID: MGI:1098221
img Jax MP, Pubmed Id: 12923163, MOUSE PHENOTYPE ID: MGI:1195264
img Jax MP, Pubmed Id: 23026748, MOUSE PHENOTYPE ID: MGI:1914342
img Jax MP, Pubmed Id: 17767905, MOUSE PHENOTYPE ID: MGI:1276534
img Jax MP, Pubmed Id: 9233792, MOUSE PHENOTYPE ID: MGI:105083
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0011468abnormal urine amino acid level0self