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Details
Link-It Detail - Jax Mouse Phenotype - irregular coat pigmentation
Debug Stats
  • ### Total Build Time: 58 ms 16.021 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 382 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=1 ms Completed: 1 ms rowSize= 183 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=4 ms Completed: 4 ms rowSize= 586 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.014 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.914 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=48 ms Completed: 48 ms rowSize= 9.660 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.165 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
irregular coat pigmentation MP:0000372
Definition (1)
uneven coloration of the hair
Parents (1)
img abnormal coat/hair pigmentation MP:0002075
Children (2)
img variegated coat color MP:0005366
img transverse fur striping MP:0010231
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img integument phenotype MP:00107717img abnormal coat/hair pigmentation MP:0002075
img mammalian phenotype MP:0000001img pigmentation phenotype MP:00011864img abnormal coat/hair pigmentation MP:0002075
Genes (17)

Species:
human : 17
SpeciesGeneGeneIdGene NameEvidence
HumanTRAPPC6A79090trafficking protein particle complex 6A
Click here to display 76 evidence detail records.
HumanMCOLN355283mucolipin 3
INFERRED
HumanSLC45A251151solute carrier family 45, member 2
Click here to display 76 evidence detail records.
HumanNSDHL50814NAD(P) dependent steroid dehydrogenase-like
Click here to display 76 evidence detail records.
HumanSMARCA58467SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 5
INFERRED
HumanTYR7299tyrosinase
Click here to display 76 evidence detail records.
HumanTBX156913T-box 15
Click here to display 76 evidence detail records.
HumanRPL386169ribosomal protein L38
Click here to display 76 evidence detail records.
HumanOCA24948oculocutaneous albinism II
INFERRED
HumanNTRK14914neurotrophic tyrosine kinase, receptor, type 1
INFERRED
HumanMITF4286microphthalmia-associated transcription factor
Click here to display 76 evidence detail records.
HumanKITLG4254KIT ligand
Click here to display 76 evidence detail records.
HumanKIT3815v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
Click here to display 76 evidence detail records.
HumanHTR2C33585-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled
INFERRED
HumanEDA1896ectodysplasin A
Click here to display 76 evidence detail records.
HumanATP7A538ATPase, Cu++ transporting, alpha polypeptide
INFERRED
HumanASIP434agouti signaling protein
Click here to display 76 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000372irregular coat pigmentation0self