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Details
Link-It Detail - Jax Mouse Phenotype - abnormal skin pigmentation
Debug Stats
  • ### Total Build Time: 144 ms 26.756 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 380 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 271 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 186 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=3 ms Completed: 3 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= 1.014 KB
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 4.649 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 2.898 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=121 ms Completed: 121 ms rowSize= 16.068 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.164 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal skin pigmentation MP:0002095
Definition (1)
anomaly in the coloration of the skin due to changes in the amount, shape, or distribution of cells producing pigment
Synonyms (1)
"skin: pigmentation anomalies" EXACT
Parents (2)
img abnormal skin coloration MP:0011239
img pigmentation phenotype MP:0001186
Children (10)
img abnormal foot pigmentation MP:0009379
img pigment incontinence MP:0010206
img decreased skin pigmentation MP:0011627
img absent skin pigmentation MP:0001189
img variable depigmentation MP:0010016
img delayed skin pigmentation appearance MP:0010232
img abnormal epidermal pigmentation MP:0009387
img abnormal tail pigmentation MP:0005174
img abnormal ear pigmentation MP:0000015
img abnormal dermal pigmentation MP:0009385
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img integument phenotype MP:00107715img abnormal skin coloration MP:0011239
img mammalian phenotype MP:0000001img pigmentation phenotype MP:00011863img pigmentation phenotype MP:0001186
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
Click here to display 81 evidence detail records.
HumanAEBP2121536AE binding protein 2
INFERRED
HumanHPS489781Hermansky-Pudlak syndrome 4
Click here to display 81 evidence detail records.
HumanDOCK785440dedicator of cytokinesis 7
Click here to display 81 evidence detail records.
HumanADAMTS2080070ADAM metallopeptidase with thrombospondin type 1 motif, 20
Click here to display 81 evidence detail records.
HumanTTC7A57217tetratricopeptide repeat domain 7A
Click here to display 81 evidence detail records.
HumanMCOLN355283mucolipin 3
INFERRED
HumanRECQL49401RecQ protein-like 4
INFERRED
HumanBARX28538BARX homeobox 2
Click here to display 81 evidence detail records.
HumanIKBKG8517inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
INFERRED
HumanFOXN18456forkhead box N1
Click here to display 81 evidence detail records.
HumanTYR7299tyrosinase
Click here to display 81 evidence detail records.
HumanTRAF67189TNF receptor-associated factor 6, E3 ubiquitin protein ligase
Click here to display 81 evidence detail records.
HumanTFAP2A7020transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
INFERRED
HumanTBX156913T-box 15
Click here to display 81 evidence detail records.
HumanTAL16886T-cell acute lymphocytic leukemia 1
Click here to display 81 evidence detail records.
HumanSNAI26591snail family zinc finger 2
Click here to display 81 evidence detail records.
HumanRPS196223ribosomal protein S19
INFERRED
HumanRPL27A6157ribosomal protein L27a
INFERRED
HumanRAG15896recombination activating gene 1
Click here to display 81 evidence detail records.
HumanRAD9A5883RAD9 homolog A (S. pombe)
Click here to display 81 evidence detail records.
HumanPTPN65777protein tyrosine phosphatase, non-receptor type 6
Click here to display 81 evidence detail records.
HumanPOLH5429polymerase (DNA directed), eta
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002095abnormal skin pigmentation0self