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Details
Link-It Detail - Jax Mouse Phenotype - abnormal ear pigmentation
Debug Stats
  • ### Total Build Time: 30 ms 17.220 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 378 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 270 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=3 ms Completed: 3 ms rowSize= 1.022 KB
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.021 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=8 ms Completed: 8 ms rowSize= 5.593 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=14 ms Completed: 14 ms rowSize= 7.643 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.163 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal ear pigmentation MP:0000015
Definition (1)
anomaly in the coloration of the ear due to changes in the amount, shape, or distribution of cells producing pigment
Parents (2)
img abnormal outer ear morphology MP:0002177
img abnormal skin pigmentation MP:0002095
Children (2)
img increased ear pigmentation MP:0011278
img decreased ear pigmentation MP:0011279
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053826img abnormal outer ear morphology MP:0002177
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053775img abnormal outer ear morphology MP:0002177
img mammalian phenotype MP:0000001img integument phenotype MP:00107716img abnormal skin pigmentation MP:0002095
img mammalian phenotype MP:0000001img pigmentation phenotype MP:00011864img abnormal skin pigmentation MP:0002095
Genes (14)

Species:
human : 14
SpeciesGeneGeneIdGene NameEvidence
HumanBLOC1S3388552biogenesis of lysosomal organelles complex-1, subunit 3
INFERRED
HumanSLC24A5283652solute carrier family 24 (sodium/potassium/calcium exchanger), member 5
Click here to display 19 evidence detail records.
HumanHPS489781Hermansky-Pudlak syndrome 4
Click here to display 19 evidence detail records.
HumanRPL27A6157ribosomal protein L27a
INFERRED
HumanPOLH5429polymerase (DNA directed), eta
Click here to display 19 evidence detail records.
HumanMITF4286microphthalmia-associated transcription factor
INFERRED
HumanKITLG4254KIT ligand
Click here to display 19 evidence detail records.
HumanMC1R4157melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor)
INFERRED
HumanKRT23849keratin 2
INFERRED
HumanKIT3815v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
Click here to display 19 evidence detail records.
HumanHPS13257Hermansky-Pudlak syndrome 1
INFERRED
HumanGNAQ2776guanine nucleotide binding protein (G protein), q polypeptide
INFERRED
HumanGNA112767guanine nucleotide binding protein (G protein), alpha 11 (Gq class)
INFERRED
HumanCBL867Cbl proto-oncogene, E3 ubiquitin protein ligase
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000015abnormal ear pigmentation0self