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Details
Link-It Detail - Jax Mouse Phenotype - integument phenotype
Debug Stats
  • ### Total Build Time: 74 ms 21.648 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 368 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 342 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 184 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=0 Completed: 0 ms rowSize= 574 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 2.387 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.145 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=67 ms Completed: 67 ms rowSize= 15.381 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.158 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
integument phenotype MP:0010771
Definition (1)
the observable morphological and physiological characteristics of the skin and its associated structures, such as the hair, nails, sweat glands, sebaceous glands and other secretory glands
Synonyms (1)
"touch/vibrissae phenotype" NARROW
Parents (1)
img mammalian phenotype MP:0000001
Children (5)
img abnormal skin adnexa physiology MP:0010680
img abnormal skin morphology MP:0002060
img abnormal skin adnexa morphology MP:0010678
img abnormal skin physiology MP:0005501
img abnormal touch/ nociception MP:0001968
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:00000012img mammalian phenotype MP:0000001
Genes (1221)

Species:
human : 1221
Page Size
Current 25
  Page 1 of 49
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanC8orf44-SGK3100533105
INFERRED
HumanMINOS1-NBL1100532736
INFERRED
HumanTIMM23100287932translocase of inner mitochondrial membrane 23 homolog (yeast)
INFERRED
HumanCDK11A728642cyclin-dependent kinase 11A
INFERRED
HumanAREGB727738amphiregulin B
INFERRED
HumanGPR89A653519G protein-coupled receptor 89A
INFERRED
HumanNCF1653361neutrophil cytosolic factor 1
INFERRED
HumanPIRT644139phosphoinositide-interacting regulator of transient receptor potential channels
INFERRED
HumanCISD2493856CDGSH iron sulfur domain 2
INFERRED
HumanBSX390259brain-specific homeobox
INFERRED
HumanBLOC1S3388552biogenesis of lysosomal organelles complex-1, subunit 3
INFERRED
HumanMIA3375056melanoma inhibitory activity family, member 3
INFERRED
HumanHCN1348980hyperpolarization activated cyclic nucleotide-gated potassium channel 1
INFERRED
HumanTBX10347853T-box 10
INFERRED
HumanFREM2341640FRAS1 related extracellular matrix protein 2
INFERRED
HumanZDHHC21340481zinc finger, DHHC-type containing 21
INFERRED
HumanRSPO2340419R-spondin 2
INFERRED
HumanTREML1340205triggering receptor expressed on myeloid cells-like 1
INFERRED
HumanIFNE338376interferon, epsilon
INFERRED
HumanSH3PXD2B285590SH3 and PX domains 2B
INFERRED
HumanSLC24A5283652solute carrier family 24 (sodium/potassium/calcium exchanger), member 5
INFERRED
HumanNPB256933neuropeptide B
INFERRED
HumanSLC17A8246213solute carrier family 17 (vesicular glutamate transporter), member 8
INFERRED
HumanGPRC6A222545G protein-coupled receptor, family C, group 6, member A
INFERRED
HumanCERS3204219ceramide synthase 3
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0010771integument phenotype0self