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Details
Link-It Detail - Jax Mouse Phenotype - abnormal vitamin A metabolism
Debug Stats
  • ### Total Build Time: 15 ms 38.753 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 386 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 388 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 186 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 583 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 584 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.582 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 33.782 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.167 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal vitamin A metabolism MP:0011233
Definition (1)
altered ability to metabolize any of the vitamin A compounds, retinol, retinal (retinaldehyde) and retinoic acid; animals can not synthesize vitamin A de novo, but form it through oxidative cleavage of carotenoids supplied in the diet
Synonyms (1)
"abnormal retinal metabolism" NARROW
Parents (1)
img abnormal vitamin homeostasis MP:0004019
Children (1)
img abnormal retinol metabolism MP:0005444
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053765img abnormal vitamin homeostasis MP:0004019
Genes (8)

Species:
human : 8
SpeciesGeneGeneIdGene NameEvidence
HumanRDH10157506retinol dehydrogenase 10 (all-trans)
img Jax MP, Pubmed Id: 22319578, MOUSE PHENOTYPE ID: MGI:1924238
img Jax MP, Pubmed Id: 17933883, MOUSE PHENOTYPE ID: MGI:98001
img Jax MP, Pubmed Id: 22319578, MOUSE PHENOTYPE ID: MGI:1924238
img Jax MP, Pubmed Id: 22319578, MOUSE PHENOTYPE ID: MGI:107928
img Jax MP, Pubmed Id: 18606814, MOUSE PHENOTYPE ID: MGI:87920
img Jax MP, Pubmed Id: 17933883, MOUSE PHENOTYPE ID: MGI:98001
img Jax MP, Pubmed Id: 14684738, MOUSE PHENOTYPE ID: MGI:1891259
img Jax MP, Pubmed Id: 18606814, MOUSE PHENOTYPE ID: MGI:87920
HumanLRAT9227lecithin retinol acyltransferase (phosphatidylcholine--retinol O-acyltransferase)
img Jax MP, Pubmed Id: 22319578, MOUSE PHENOTYPE ID: MGI:1924238
img Jax MP, Pubmed Id: 22319578, MOUSE PHENOTYPE ID: MGI:1924238
img Jax MP, Pubmed Id: 17933883, MOUSE PHENOTYPE ID: MGI:98001
img Jax MP, Pubmed Id: 14684738, MOUSE PHENOTYPE ID: MGI:1891259
img Jax MP, Pubmed Id: 18606814, MOUSE PHENOTYPE ID: MGI:87920
img Jax MP, Pubmed Id: 17933883, MOUSE PHENOTYPE ID: MGI:98001
img Jax MP, Pubmed Id: 22319578, MOUSE PHENOTYPE ID: MGI:107928
img Jax MP, Pubmed Id: 18606814, MOUSE PHENOTYPE ID: MGI:87920
HumanALDH1A28854aldehyde dehydrogenase 1 family, member A2
img Jax MP, Pubmed Id: 18606814, MOUSE PHENOTYPE ID: MGI:87920
img Jax MP, Pubmed Id: 17933883, MOUSE PHENOTYPE ID: MGI:98001
img Jax MP, Pubmed Id: 22319578, MOUSE PHENOTYPE ID: MGI:1924238
img Jax MP, Pubmed Id: 22319578, MOUSE PHENOTYPE ID: MGI:1924238
img Jax MP, Pubmed Id: 22319578, MOUSE PHENOTYPE ID: MGI:107928
img Jax MP, Pubmed Id: 17933883, MOUSE PHENOTYPE ID: MGI:98001
img Jax MP, Pubmed Id: 14684738, MOUSE PHENOTYPE ID: MGI:1891259
img Jax MP, Pubmed Id: 18606814, MOUSE PHENOTYPE ID: MGI:87920
HumanTTR7276transthyretin
INFERRED
HumanRPE656121retinal pigment epithelium-specific protein 65kDa
img Jax MP, Pubmed Id: 18606814, MOUSE PHENOTYPE ID: MGI:87920
img Jax MP, Pubmed Id: 22319578, MOUSE PHENOTYPE ID: MGI:107928
img Jax MP, Pubmed Id: 17933883, MOUSE PHENOTYPE ID: MGI:98001
img Jax MP, Pubmed Id: 14684738, MOUSE PHENOTYPE ID: MGI:1891259
img Jax MP, Pubmed Id: 22319578, MOUSE PHENOTYPE ID: MGI:1924238
img Jax MP, Pubmed Id: 18606814, MOUSE PHENOTYPE ID: MGI:87920
img Jax MP, Pubmed Id: 22319578, MOUSE PHENOTYPE ID: MGI:1924238
img Jax MP, Pubmed Id: 17933883, MOUSE PHENOTYPE ID: MGI:98001
HumanRBP15947retinol binding protein 1, cellular
INFERRED
HumanADH1C126alcohol dehydrogenase 1C (class I), gamma polypeptide
INFERRED
HumanPLIN2123perilipin 2
img Jax MP, Pubmed Id: 18606814, MOUSE PHENOTYPE ID: MGI:87920
img Jax MP, Pubmed Id: 22319578, MOUSE PHENOTYPE ID: MGI:107928
img Jax MP, Pubmed Id: 14684738, MOUSE PHENOTYPE ID: MGI:1891259
img Jax MP, Pubmed Id: 17933883, MOUSE PHENOTYPE ID: MGI:98001
img Jax MP, Pubmed Id: 18606814, MOUSE PHENOTYPE ID: MGI:87920
img Jax MP, Pubmed Id: 22319578, MOUSE PHENOTYPE ID: MGI:1924238
img Jax MP, Pubmed Id: 22319578, MOUSE PHENOTYPE ID: MGI:1924238
img Jax MP, Pubmed Id: 17933883, MOUSE PHENOTYPE ID: MGI:98001
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0011233abnormal vitamin A metabolism0self