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Details
Link-It Detail - Jax Mouse Phenotype - abnormal ear pigmentation
Debug Stats
  • ### Total Build Time: 37 ms 17.220 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 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=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 1.022 KB
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.021 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 5.593 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=17 ms Completed: 17 ms rowSize= 7.643 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 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 skin pigmentation MP:0002095
img abnormal outer ear morphology MP:0002177
Children (2)
img increased ear pigmentation MP:0011278
img decreased ear pigmentation MP:0011279
Ancestral Roots
RootRoot Plus OneDepthParent
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
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
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