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Details
Link-It Detail - Jax Mouse Phenotype - pigmentation phenotype
Debug Stats
  • ### Total Build Time: 28 ms 24.376 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 372 bytes
  • CONCEPT_SOLR_HIT_STATS gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 574 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 6.003 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.145 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=22 ms Completed: 22 ms rowSize= 15 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.160 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
pigmentation phenotype MP:0001186
Parents (1)
img mammalian phenotype MP:0000001
Children (13)
img hypopigmentation MP:0005408
img abnormal melanocyte proliferation MP:0010741
img abnormal melanogenesis MP:0005077
img abnormal digit pigmentation MP:0000569
img abnormal coat/hair pigmentation MP:0002075
img lipofuscinosis MP:0008842
img abnormal skin pigmentation MP:0002095
img hyperpigmentation MP:0001188
img abnormal scrotum pigmentation MP:0009847
img abnormal extracutaneous pigmentation MP:0009389
img abnormal pigmentation pattern MP:0011494
img abnormal melanosome transport MP:0008834
img abnormal melanocyte morphology MP:0002877
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:00000012img mammalian phenotype MP:0000001
Genes (277)

Species:
human : 277
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED
HumanGPR89A653519G protein-coupled receptor 89A
INFERRED
HumanCISD2493856CDGSH iron sulfur domain 2
INFERRED
HumanBLOC1S3388552biogenesis of lysosomal organelles complex-1, subunit 3
INFERRED
HumanNHLRC1378884NHL repeat containing 1
INFERRED
HumanTBX10347853T-box 10
INFERRED
HumanFREM2341640FRAS1 related extracellular matrix protein 2
INFERRED
HumanZDHHC21340481zinc finger, DHHC-type containing 21
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
HumanLIPH200879lipase, member H
INFERRED
HumanMPZL3196264myelin protein zero-like 3
INFERRED
HumanLCA5167691Leber congenital amaurosis 5
INFERRED
HumanDSG4147409desmoglein 4
INFERRED
HumanEDARADD128178EDAR-associated death domain
INFERRED
HumanSPNS2124976spinster homolog 2 (Drosophila)
INFERRED
HumanAEBP2121536AE binding protein 2
INFERRED
HumanLRRK2120892leucine-rich repeat kinase 2
INFERRED
HumanC1QTNF5114902C1q and tumor necrosis factor related protein 5
INFERRED
HumanHPS489781Hermansky-Pudlak syndrome 4
INFERRED
HumanDOCK785440dedicator of cytokinesis 7
INFERRED
HumanHPS384343Hermansky-Pudlak syndrome 3
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001186pigmentation phenotype0self