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Details
Link-It Detail - Jax Mouse Phenotype - decreased tail pigmentation
Debug Stats
  • ### Total Build Time: 226 ms 12.116 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 382 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 221 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 179 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=2 ms Completed: 2 ms rowSize= 1.010 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 5.572 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=214 ms Completed: 214 ms rowSize= 3.453 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.165 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
decreased tail pigmentation MP:0011277
Definition (1)
visually detectable dilution of pigment present on the tail surface
Synonyms (1)
"tail hypopigmentation" EXACT
Parents (2)
img abnormal tail pigmentation MP:0005174
img hypopigmentation MP:0005408
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img integument phenotype MP:00107717img abnormal tail pigmentation MP:0005174
img mammalian phenotype MP:0000001img pigmentation phenotype MP:00011865img abnormal tail pigmentation MP:0005174
img mammalian phenotype MP:0000001img limbs/digits/tail phenotype MP:00053715img abnormal tail pigmentation MP:0005174
img mammalian phenotype MP:0000001img pigmentation phenotype MP:00011864img hypopigmentation MP:0005408
Genes (5)

Species:
human : 5
SpeciesGeneGeneIdGene NameEvidence
HumanBLOC1S3388552biogenesis of lysosomal organelles complex-1, subunit 3
Click here to display 40 evidence detail records.
HumanPAX35077paired box 3
Click here to display 40 evidence detail records.
HumanMITF4286microphthalmia-associated transcription factor
Click here to display 40 evidence detail records.
HumanMC1R4157melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor)
Click here to display 40 evidence detail records.
HumanHPS13257Hermansky-Pudlak syndrome 1
Click here to display 40 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0011277decreased tail pigmentation0self