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Details
Link-It Detail - Jax Mouse Phenotype - decreased eye pigmentation
Debug Stats
  • ### Total Build Time: 86 ms 16.126 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 380 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 318 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 182 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=5 ms Completed: 5 ms rowSize= 1.009 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=9 ms Completed: 9 ms rowSize= 4.229 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=69 ms Completed: 69 ms rowSize= 8.712 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.164 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
decreased eye pigmentation MP:0005172
Definition (1)
the eye has less pigmentation than normal with a possible range of color from dark red, somewhat reduced in pigment, to pink, typical of albinism or ocular albinism
Synonyms (1)
"reduced eye pigmentation" EXACT
Parents (2)
img abnormal eye pigmentation MP:0001324
img hypopigmentation MP:0005408
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
img mammalian phenotype MP:0000001img pigmentation phenotype MP:00011864img hypopigmentation MP:0005408
Genes (14)

Species:
human : 14
SpeciesGeneGeneIdGene NameEvidence
HumanVSX2338917visual system homeobox 2
Click here to display 139 evidence detail records.
HumanHPS679803Hermansky-Pudlak syndrome 6
Click here to display 139 evidence detail records.
HumanSEMA4A64218sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A
Click here to display 139 evidence detail records.
HumanBLOC1S455330biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino
Click here to display 139 evidence detail records.
HumanRAB3823682RAB38, member RAS oncogene family
Click here to display 139 evidence detail records.
HumanAP3D18943adaptor-related protein complex 3, delta 1 subunit
Click here to display 139 evidence detail records.
HumanAP3B18546adaptor-related protein complex 3, beta 1 subunit
Click here to display 139 evidence detail records.
HumanTYR7299tyrosinase
Click here to display 139 evidence detail records.
HumanPAX65080paired box 6
Click here to display 139 evidence detail records.
HumanOCA24948oculocutaneous albinism II
Click here to display 139 evidence detail records.
HumanNF14763neurofibromin 1
Click here to display 139 evidence detail records.
HumanMITF4286microphthalmia-associated transcription factor
Click here to display 139 evidence detail records.
HumanHPS13257Hermansky-Pudlak syndrome 1
Click here to display 139 evidence detail records.
HumanLYST1130lysosomal trafficking regulator
Click here to display 139 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0005172decreased eye pigmentation0self