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Details
Link-It Detail - Jax Mouse Phenotype - abnormal extracutaneous pigmentation
Debug Stats
  • ### Total Build Time: 27 ms 20.800 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 400 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 306 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
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  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 577 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 1.945 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.566 KB
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  • CONCEPT_GENES gt=27 ms Completed: 27 ms rowSize= 14.717 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.174 KB
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Jax Mouse Phenotype (1)
abnormal extracutaneous pigmentation MP:0009389
Definition (1)
anomaly in the coloration of organs and tissues excluding the integument due to changes in the amount, shape, or distribution of cells producing pigment
Parents (1)
img pigmentation phenotype MP:0001186
Children (4)
img abnormal eye pigmentation MP:0001324
img abnormal otic pigmentation MP:0009390
img abnormal leptomeninges pigmentation MP:0009391
img abnormal Harderian gland pigmentation MP:0003798
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img pigmentation phenotype MP:00011863img pigmentation phenotype MP:0001186
Genes (123)

Species:
human : 123
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED
HumanBLOC1S3388552biogenesis of lysosomal organelles complex-1, subunit 3
INFERRED
HumanVSX2338917visual system homeobox 2
INFERRED
HumanCRB2286204crumbs homolog 2 (Drosophila)
INFERRED
HumanSLC24A5283652solute carrier family 24 (sodium/potassium/calcium exchanger), member 5
INFERRED
HumanNPHP4261734nephronophthisis 4
INFERRED
HumanTBC1D32221322TBC1 domain family, member 32
INFERRED
HumanLCA5167691Leber congenital amaurosis 5
INFERRED
HumanSPNS2124976spinster homolog 2 (Drosophila)
INFERRED
HumanC1QTNF5114902C1q and tumor necrosis factor related protein 5
INFERRED
HumanHPS489781Hermansky-Pudlak syndrome 4
INFERRED
HumanHPS384343Hermansky-Pudlak syndrome 3
INFERRED
HumanDTNBP184062dystrobrevin binding protein 1
INFERRED
HumanMFRP83552membrane frizzled-related protein
INFERRED
HumanNUAK281788NUAK family, SNF1-like kinase, 2
INFERRED
HumanFUZ80199fuzzy planar cell polarity protein
INFERRED
HumanCEP29080184centrosomal protein 290kDa
INFERRED
HumanHPS679803Hermansky-Pudlak syndrome 6
INFERRED
HumanTRAPPC6A79090trafficking protein particle complex 6A
INFERRED
HumanMLPH79083melanophilin
INFERRED
HumanKXD179036KxDL motif containing 1
INFERRED
HumanPHACTR465979phosphatase and actin regulator 4
INFERRED
HumanVPS33A65082vacuolar protein sorting 33 homolog A (S. cerevisiae)
INFERRED
HumanSEMA4A64218sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A
INFERRED
HumanSMOC164093SPARC related modular calcium binding 1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0009389abnormal extracutaneous pigmentation0self