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Details
Link-It Detail - Jax Mouse Phenotype - abnormal skin development
Debug Stats
  • ### Total Build Time: 55 ms 17.133 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 378 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 228 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=0 Completed: 0 ms rowSize= 579 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 1.931 KB
  • 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=50 ms Completed: 50 ms rowSize= 11.171 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.163 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal skin development MP:0003941
Definition (1)
anomaly in the formation of the membranous protective covering of the body
Parents (1)
img abnormal skin morphology MP:0002060
Children (4)
img delayed skin barrier formation MP:0009441
img abnormal dermatome morphology MP:0003940
img abnormal epidermal stem cell morphology MP:0011004
img fetal bleb MP:0008856
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img integument phenotype MP:00107714img abnormal skin morphology MP:0002060
Genes (20)

Species:
human : 20
SpeciesGeneGeneIdGene NameEvidence
HumanGPR89A653519G protein-coupled receptor 89A
Click here to display 16 evidence detail records.
HumanFREM2341640FRAS1 related extracellular matrix protein 2
INFERRED
HumanCERS3204219ceramide synthase 3
Click here to display 16 evidence detail records.
HumanMOB1B92597MOB kinase activator 1B
INFERRED
HumanFRAS180144Fraser syndrome 1
INFERRED
HumanGPR89B51463G protein-coupled receptor 89B
Click here to display 16 evidence detail records.
HumanCRIM151232cysteine rich transmembrane BMP regulator 1 (chordin-like)
INFERRED
HumanABHD551099abhydrolase domain containing 5
Click here to display 16 evidence detail records.
HumanABCA1226154ATP-binding cassette, sub-family A (ABC1), member 12
Click here to display 16 evidence detail records.
HumanYAP110413Yes-associated protein 1
INFERRED
HumanTP638626tumor protein p63
Click here to display 16 evidence detail records.
HumanVDR7421vitamin D (1,25- dihydroxyvitamin D3) receptor
Click here to display 16 evidence detail records.
HumanTGM37053transglutaminase 3
INFERRED
HumanTERF17013telomeric repeat binding factor (NIMA-interacting) 1
Click here to display 16 evidence detail records.
HumanTCF156939transcription factor 15 (basic helix-loop-helix)
INFERRED
HumanPDGFRA5156platelet-derived growth factor receptor, alpha polypeptide
INFERRED
HumanIRF63664interferon regulatory factor 6
Click here to display 16 evidence detail records.
HumanCDKN2A1029cyclin-dependent kinase inhibitor 2A
Click here to display 16 evidence detail records.
HumanCDKN1A1026cyclin-dependent kinase inhibitor 1A (p21, Cip1)
Click here to display 16 evidence detail records.
HumanCDK71022cyclin-dependent kinase 7
Click here to display 16 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003941abnormal skin development0self