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Details
Link-It Detail - Jax Mouse Phenotype - abnormal skin pigmentation
Debug Stats
  • ### Total Build Time: 124 ms 26.759 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 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= 189 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=2 ms Completed: 2 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=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=105 ms Completed: 105 ms rowSize= 16.068 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 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)
"abnormal cutaneous pigmentation" 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