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Details
Link-It Detail - Jax Mouse Phenotype - abnormal epidermis stratum basale morphology
Debug Stats
  • ### Total Build Time: 61 ms 22.809 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 416 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 276 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 192 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 590 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.486 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 1.577 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=53 ms Completed: 53 ms rowSize= 16.979 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.182 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal epidermis stratum basale morphology MP:0001231
Definition (1)
any structural anomaly of the deepest layer of the epidermis, which is composed of dividing stem cells and anchoring cells
Synonyms (1)
"abnormal palisade layer morphology" EXACT
Parents (1)
img abnormal epidermal layer morphology MP:0001216
Children (3)
img thick epidermis stratum basale MP:0009715
img thin epidermis stratum basale MP:0009714
img absent epidermis stratum basale MP:0001232
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img integument phenotype MP:00107715img abnormal epidermal layer morphology MP:0001216
Genes (35)

Species:
human : 35
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SpeciesGeneGeneIdGene NameEvidence
HumanGPR89A653519G protein-coupled receptor 89A
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HumanCD109135228CD109 molecule
INFERRED
HumanSHARPIN81858SHANK-associated RH domain interactor
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HumanSAV160485salvador homolog 1 (Drosophila)
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HumanGRHL357822grainyhead-like 3 (Drosophila)
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HumanCYP26B156603cytochrome P450, family 26, subfamily B, polypeptide 1
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HumanSUFU51684suppressor of fused homolog (Drosophila)
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HumanGPR89B51463G protein-coupled receptor 89B
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HumanABCA1226154ATP-binding cassette, sub-family A (ABC1), member 12
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HumanMORF4L110933mortality factor 4 like 1
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HumanYAP110413Yes-associated protein 1
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HumanIKBKG8517inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
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HumanTCF7L26934transcription factor 7-like 2 (T-cell specific, HMG-box)
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HumanRELA5970v-rel avian reticuloendotheliosis viral oncogene homolog A
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HumanMAPK85599mitogen-activated protein kinase 8
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HumanPLEC5339plectin
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HumanNFKBIA4792nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha
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HumanLMNA4000lamin A/C
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HumanLAMA33909laminin, alpha 3
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HumanKRT143861keratin 14
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HumanKRT103858keratin 10
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HumanITGB43691integrin, beta 4
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HumanIRF63664interferon regulatory factor 6
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HumanGLI32737GLI family zinc finger 3
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HumanFGFR22263fibroblast growth factor receptor 2
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XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001231abnormal epidermis stratum basale morphology0self