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Details
Link-It Detail - Jax Mouse Phenotype - abnormal ciliary body pigmentation
Debug Stats
  • ### Total Build Time: 82 ms 19.354 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 396 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 264 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=34 ms Completed: 34 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=12 ms Completed: 12 ms rowSize= 597 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 2.936 KB
  • CONCEPT_RELATIONSHIPS gt=2 ms Completed: 2 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=23 ms Completed: 23 ms rowSize= 13.866 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.172 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal ciliary body pigmentation MP:0005101
Definition (1)
anomalous coloring of the thickened portion of the vascular tunic, which lies between the choroid and the iris
Parents (1)
img abnormal eye pigment epithelium morphology MP:0005200
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img vision/eye phenotype MP:00053916img abnormal eye pigment epithelium morphology MP:0005200
img mammalian phenotype MP:0000001img pigmentation phenotype MP:00011866img abnormal eye pigment epithelium morphology MP:0005200
Genes (4)

Species:
human : 4
SpeciesGeneGeneIdGene NameEvidence
HumanSLC24A5283652solute carrier family 24 (sodium/potassium/calcium exchanger), member 5
img Jax MP, Pubmed Id: 11092754, MOUSE PHENOTYPE ID: MGI:107193
img Jax MP, Pubmed Id: 18424845, MOUSE PHENOTYPE ID: MGI:2677271
img Jax MP, Pubmed Id: 102659, MOUSE PHENOTYPE ID: MGI:2177763
img Jax MP, Pubmed Id: 13943454, MOUSE PHENOTYPE ID: MGI:107448
HumanGPR1434935G protein-coupled receptor 143
img Jax MP, Pubmed Id: 11092754, MOUSE PHENOTYPE ID: MGI:107193
img Jax MP, Pubmed Id: 18424845, MOUSE PHENOTYPE ID: MGI:2677271
img Jax MP, Pubmed Id: 13943454, MOUSE PHENOTYPE ID: MGI:107448
img Jax MP, Pubmed Id: 102659, MOUSE PHENOTYPE ID: MGI:2177763
HumanHPS13257Hermansky-Pudlak syndrome 1
img Jax MP, Pubmed Id: 18424845, MOUSE PHENOTYPE ID: MGI:2677271
img Jax MP, Pubmed Id: 11092754, MOUSE PHENOTYPE ID: MGI:107193
img Jax MP, Pubmed Id: 13943454, MOUSE PHENOTYPE ID: MGI:107448
img Jax MP, Pubmed Id: 102659, MOUSE PHENOTYPE ID: MGI:2177763
HumanLYST1130lysosomal trafficking regulator
img Jax MP, Pubmed Id: 11092754, MOUSE PHENOTYPE ID: MGI:107193
img Jax MP, Pubmed Id: 102659, MOUSE PHENOTYPE ID: MGI:2177763
img Jax MP, Pubmed Id: 18424845, MOUSE PHENOTYPE ID: MGI:2677271
img Jax MP, Pubmed Id: 13943454, MOUSE PHENOTYPE ID: MGI:107448
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0005101abnormal ciliary body pigmentation0self