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Details
Link-It Detail - Jax Mouse Phenotype - impaired skin barrier function
Debug Stats
  • ### Total Build Time: 392 ms 23.110 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 388 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 238 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=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=12 ms Completed: 12 ms rowSize= 1.017 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=12 ms Completed: 12 ms rowSize= 2.911 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=359 ms Completed: 359 ms rowSize= 17.251 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.168 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
impaired skin barrier function MP:0002796
Definition (1)
impaired ability of the skin to regulate water loss; frequently leads to dehydration
Parents (2)
img abnormal skin physiology MP:0005501
img abnormal fluid regulation MP:0001784
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img integument phenotype MP:00107714img abnormal skin physiology MP:0005501
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053765img abnormal fluid regulation MP:0001784
Genes (49)

Species:
human : 49
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Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanGPR89A653519G protein-coupled receptor 89A
Click here to display 95 evidence detail records.
HumanCERS3204219ceramide synthase 3
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HumanDGAT284649diacylglycerol O-acyltransferase 2
Click here to display 95 evidence detail records.
HumanELOVL383401ELOVL fatty acid elongase 3
Click here to display 95 evidence detail records.
HumanBCL11B64919B-cell CLL/lymphoma 11B (zinc finger protein)
Click here to display 95 evidence detail records.
HumanSAV160485salvador homolog 1 (Drosophila)
Click here to display 95 evidence detail records.
HumanALOXE359344arachidonate lipoxygenase 3
Click here to display 95 evidence detail records.
HumanGRHL357822grainyhead-like 3 (Drosophila)
Click here to display 95 evidence detail records.
HumanCYP26B156603cytochrome P450, family 26, subfamily B, polypeptide 1
Click here to display 95 evidence detail records.
HumanROBO454538roundabout, axon guidance receptor, homolog 4 (Drosophila)
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HumanGPR89B51463G protein-coupled receptor 89B
Click here to display 95 evidence detail records.
HumanABHD551099abhydrolase domain containing 5
Click here to display 95 evidence detail records.
HumanABCA1226154ATP-binding cassette, sub-family A (ABC1), member 12
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HumanCASP1423581caspase 14, apoptosis-related cysteine peptidase
Click here to display 95 evidence detail records.
HumanSPINK511005serine peptidase inhibitor, Kazal type 5
Click here to display 95 evidence detail records.
HumanSLC27A410999solute carrier family 27 (fatty acid transporter), member 4
Click here to display 95 evidence detail records.
HumanPTGES310728prostaglandin E synthase 3 (cytosolic)
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HumanYAP110413Yes-associated protein 1
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HumanKLF49314Kruppel-like factor 4 (gut)
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HumanRASSF99182Ras association (RalGDS/AF-6) domain family (N-terminal) member 9
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HumanCLDN19076claudin 1
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HumanTP638626tumor protein p63
Click here to display 95 evidence detail records.
HumanNSMAF8439neutral sphingomyelinase (N-SMase) activation associated factor
Click here to display 95 evidence detail records.
HumanTNFRSF1A7132tumor necrosis factor receptor superfamily, member 1A
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HumanTERF17013telomeric repeat binding factor (NIMA-interacting) 1
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XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002796impaired skin barrier function0self