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Details
Link-It Detail - Jax Mouse Phenotype - abnormal skin coloration
Debug Stats
  • ### Total Build Time: 61 ms 18.825 KB
  • CONCEPT_NAME gt=9 ms Completed: 9 ms rowSize= 376 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
  • CONCEPT_TEXT gt=NONE 1 ms Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=15 ms Completed: 15 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= 579 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 583 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.566 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=26 ms Completed: 26 ms rowSize= 14.187 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.162 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal skin coloration MP:0011239
Definition (1)
a variation in an expected skin color or complexion that may be due to inflammation, pigment defects or other causes
Parents (1)
img abnormal skin morphology MP:0002060
Children (1)
img abnormal skin pigmentation MP:0002095
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img integument phenotype MP:00107714img abnormal skin morphology MP:0002060
Genes (53)

Species:
human : 53
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanBLOC1S3388552biogenesis of lysosomal organelles complex-1, subunit 3
INFERRED
HumanSLC24A5283652solute carrier family 24 (sodium/potassium/calcium exchanger), member 5
INFERRED
HumanDSG4147409desmoglein 4
INFERRED
HumanAEBP2121536AE binding protein 2
INFERRED
HumanHPS489781Hermansky-Pudlak syndrome 4
INFERRED
HumanDOCK785440dedicator of cytokinesis 7
INFERRED
HumanADAMTS2080070ADAM metallopeptidase with thrombospondin type 1 motif, 20
INFERRED
HumanTTC7A57217tetratricopeptide repeat domain 7A
INFERRED
HumanMCOLN355283mucolipin 3
INFERRED
HumanRECQL49401RecQ protein-like 4
INFERRED
HumanBARX28538BARX homeobox 2
INFERRED
HumanIKBKG8517inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
INFERRED
HumanFOXN18456forkhead box N1
INFERRED
HumanTYR7299tyrosinase
INFERRED
HumanTRAF67189TNF receptor-associated factor 6, E3 ubiquitin protein ligase
INFERRED
HumanTFAP2A7020transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
INFERRED
HumanTBX156913T-box 15
INFERRED
HumanTAL16886T-cell acute lymphocytic leukemia 1
INFERRED
HumanSNAI26591snail family zinc finger 2
INFERRED
HumanRPS196223ribosomal protein S19
INFERRED
HumanRPL27A6157ribosomal protein L27a
INFERRED
HumanRAG15896recombination activating gene 1
INFERRED
HumanRAD9A5883RAD9 homolog A (S. pombe)
INFERRED
HumanPTPN65777protein tyrosine phosphatase, non-receptor type 6
INFERRED
HumanPOLH5429polymerase (DNA directed), eta
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0011239abnormal skin coloration0self