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Details
Link-It Detail - Jax Mouse Phenotype - abnormal intestinal mineral absorption
Debug Stats
  • ### Total Build Time: 33 ms 31.188 KB
  • CONCEPT_NAME gt=11 ms Completed: 11 ms rowSize= 404 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 317 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=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= 585 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 595 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 1.582 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=13 ms Completed: 13 ms rowSize= 26.429 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.176 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal intestinal mineral absorption MP:0001670
Definition (1)
any anomaly in the ability of the body to take up inorganic substances that have importance in body functions into the blood by absorption from the small intestine
Parents (1)
img abnormal intestinal absorption MP:0001666
Children (1)
img abnormal intestinal calcium absorption MP:0011219
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img digestive/alimentary phenotype MP:00053816img abnormal intestinal absorption MP:0001666
Genes (9)

Species:
human : 9
SpeciesGeneGeneIdGene NameEvidence
HumanTMPRSS6164656transmembrane protease, serine 6
img Jax MP, Pubmed Id: 17954933, MOUSE PHENOTYPE ID: MGI:1913750
img Jax MP, Pubmed Id: 10192390, MOUSE PHENOTYPE ID: MGI:98822
img Jax MP, Pubmed Id: 15007064, MOUSE PHENOTYPE ID: MGI:96705
img Jax MP, Pubmed Id: 9566988, MOUSE PHENOTYPE ID: MGI:3052801
img Jax MP, Pubmed Id: 18451267, MOUSE PHENOTYPE ID: MGI:1919003
img Jax MP, Pubmed Id: 9566988, MOUSE PHENOTYPE ID: MGI:97171
HumanSLC30A7148867solute carrier family 30 (zinc transporter), member 7
img Jax MP, Pubmed Id: 9566988, MOUSE PHENOTYPE ID: MGI:97171
img Jax MP, Pubmed Id: 10192390, MOUSE PHENOTYPE ID: MGI:98822
img Jax MP, Pubmed Id: 15007064, MOUSE PHENOTYPE ID: MGI:96705
img Jax MP, Pubmed Id: 18451267, MOUSE PHENOTYPE ID: MGI:1919003
img Jax MP, Pubmed Id: 17954933, MOUSE PHENOTYPE ID: MGI:1913750
img Jax MP, Pubmed Id: 9566988, MOUSE PHENOTYPE ID: MGI:3052801
HumanTRPV655503transient receptor potential cation channel, subfamily V, member 6
INFERRED
HumanVDR7421vitamin D (1,25- dihydroxyvitamin D3) receptor
INFERRED
HumanTFRC7037transferrin receptor (p90, CD71)
img Jax MP, Pubmed Id: 15007064, MOUSE PHENOTYPE ID: MGI:96705
img Jax MP, Pubmed Id: 9566988, MOUSE PHENOTYPE ID: MGI:97171
img Jax MP, Pubmed Id: 9566988, MOUSE PHENOTYPE ID: MGI:3052801
img Jax MP, Pubmed Id: 18451267, MOUSE PHENOTYPE ID: MGI:1919003
img Jax MP, Pubmed Id: 10192390, MOUSE PHENOTYPE ID: MGI:98822
img Jax MP, Pubmed Id: 17954933, MOUSE PHENOTYPE ID: MGI:1913750
HumanPHEX5251phosphate regulating endopeptidase homolog, X-linked
INFERRED
HumanMT1E4493metallothionein 1E
img Jax MP, Pubmed Id: 17954933, MOUSE PHENOTYPE ID: MGI:1913750
img Jax MP, Pubmed Id: 18451267, MOUSE PHENOTYPE ID: MGI:1919003
img Jax MP, Pubmed Id: 10192390, MOUSE PHENOTYPE ID: MGI:98822
img Jax MP, Pubmed Id: 15007064, MOUSE PHENOTYPE ID: MGI:96705
img Jax MP, Pubmed Id: 9566988, MOUSE PHENOTYPE ID: MGI:97171
img Jax MP, Pubmed Id: 9566988, MOUSE PHENOTYPE ID: MGI:3052801
HumanKRT83856keratin 8
img Jax MP, Pubmed Id: 9566988, MOUSE PHENOTYPE ID: MGI:97171
img Jax MP, Pubmed Id: 15007064, MOUSE PHENOTYPE ID: MGI:96705
img Jax MP, Pubmed Id: 9566988, MOUSE PHENOTYPE ID: MGI:3052801
img Jax MP, Pubmed Id: 18451267, MOUSE PHENOTYPE ID: MGI:1919003
img Jax MP, Pubmed Id: 17954933, MOUSE PHENOTYPE ID: MGI:1913750
img Jax MP, Pubmed Id: 10192390, MOUSE PHENOTYPE ID: MGI:98822
HumanEPHB62051EPH receptor B6
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001670abnormal intestinal mineral absorption0self