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Details
Link-It Detail - Jax Mouse Phenotype - absent eye pigmentation
Debug Stats
  • ### Total Build Time: 67 ms 9.908 KB
  • CONCEPT_NAME gt=3 ms Completed: 2 ms rowSize= 374 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 258 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 168 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=11 ms Completed: 11 ms rowSize= 580 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 572 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=9 ms Completed: 9 ms rowSize= 2.902 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=30 ms Completed: 30 ms rowSize= 3.794 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.161 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
absent eye pigmentation MP:0008480
Definition (1)
absence of melanin (pigment) in the eye either due to absent melanocytes or failure of melanin synthesis
Synonyms (1)
"albino eye" EXACT
Parents (1)
img abnormal eye pigmentation MP:0001324
Children (1)
img ocular albinism MP:0006159
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img vision/eye phenotype MP:00053915img abnormal eye pigmentation MP:0001324
img mammalian phenotype MP:0000001img pigmentation phenotype MP:00011865img abnormal eye pigmentation MP:0001324
Genes (6)

Species:
human : 6
SpeciesGeneGeneIdGene NameEvidence
HumanSLC24A5283652solute carrier family 24 (sodium/potassium/calcium exchanger), member 5
INFERRED
HumanHPS384343Hermansky-Pudlak syndrome 3
Click here to display 23 evidence detail records.
HumanFUZ80199fuzzy planar cell polarity protein
Click here to display 23 evidence detail records.
HumanBLOC1S626258biogenesis of lysosomal organelles complex-1, subunit 6, pallidin
INFERRED
HumanTYR7299tyrosinase
Click here to display 23 evidence detail records.
HumanMITF4286microphthalmia-associated transcription factor
Click here to display 23 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0008480absent eye pigmentation0self