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Details
Link-It Detail - Jax Mouse Phenotype - abnormal melanocyte morphology
Debug Stats
  • ### Total Build Time: 40 ms 23.446 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 388 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 210 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 178 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=3 ms Completed: 3 ms rowSize= 577 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 4.734 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.566 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=26 ms Completed: 26 ms rowSize= 14.512 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.168 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal melanocyte morphology MP:0002877
Definition (1)
any structural anomaly of the cells that produce pigment
Synonyms (1)
"abnormal melanocytes" EXACT
Parents (1)
img pigmentation phenotype MP:0001186
Children (10)
img ectopic melanocytes MP:0010037
img abnormal dermal melanocyte morphology MP:0009386
img abnormal choroid melanocyte morphology MP:0010191
img abnormal hair follicle melanocyte morphology MP:0004381
img abnormal retinal melanocyte morphology MP:0010190
img abnormal melanocyte eumelanin content MP:0012015
img abnormal strial intermediate cell morphology MP:0004367
img abnormal epidermal melanocyte morphology MP:0009388
img abnormal melanosome morphology MP:0005075
img abnormal melanocyte number MP:0012021
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img pigmentation phenotype MP:00011863img pigmentation phenotype MP:0001186
Genes (51)

Species:
human : 51
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanBLOC1S3388552biogenesis of lysosomal organelles complex-1, subunit 3
INFERRED
HumanZDHHC21340481zinc finger, DHHC-type containing 21
INFERRED
HumanSLC24A5283652solute carrier family 24 (sodium/potassium/calcium exchanger), member 5
INFERRED
HumanLIPH200879lipase, member H
INFERRED
HumanMPZL3196264myelin protein zero-like 3
INFERRED
HumanHPS489781Hermansky-Pudlak syndrome 4
INFERRED
HumanHPS384343Hermansky-Pudlak syndrome 3
INFERRED
HumanELOVL383401ELOVL fatty acid elongase 3
INFERRED
HumanADAMTS2080070ADAM metallopeptidase with thrombospondin type 1 motif, 20
INFERRED
HumanHPS679803Hermansky-Pudlak syndrome 6
INFERRED
HumanTRAPPC6A79090trafficking protein particle complex 6A
INFERRED
HumanMLPH79083melanophilin
Click here to display 34 evidence detail records.
HumanKXD179036KxDL motif containing 1
INFERRED
HumanVPS33A65082vacuolar protein sorting 33 homolog A (S. cerevisiae)
INFERRED
HumanBLOC1S563915biogenesis of lysosomal organelles complex-1, subunit 5, muted
INFERRED
HumanBLOC1S455330biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino
INFERRED
HumanLEF151176lymphoid enhancer-binding factor 1
INFERRED
HumanBLOC1S626258biogenesis of lysosomal organelles complex-1, subunit 6, pallidin
INFERRED
HumanRAB3823682RAB38, member RAS oncogene family
INFERRED
HumanBCL2L1110018BCL2-like 11 (apoptosis facilitator)
INFERRED
HumanFIG49896FIG4 homolog, SAC1 lipid phosphatase domain containing (S. cerevisiae)
INFERRED
HumanS1PR29294sphingosine-1-phosphate receptor 2
INFERRED
HumanAP3B18546adaptor-related protein complex 3, beta 1 subunit
INFERRED
HumanZBTB177709zinc finger and BTB domain containing 17
INFERRED
HumanTYRP17306tyrosinase-related protein 1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002877abnormal melanocyte morphology0self