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Details
Link-It Detail - Jax Mouse Phenotype - altered susceptibility to autoimmune disorder
Debug Stats
  • ### Total Build Time: 31 ms 20.271 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 418 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 359 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
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  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 574 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.062 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.564 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=25 ms Completed: 25 ms rowSize= 14.810 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.183 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
altered susceptibility to autoimmune disorder MP:0002425
Definition (1)
a change in the likelihood that an organism will develop disease characterized by production of antibodies that react with host tissues or immune effector cells that are autoreactive to endogenous peptides
Synonyms (1)
"autoimmune disorder susceptibility" EXACT
Parents (1)
img autoimmune response MP:0001844
Children (2)
img decreased susceptibility to autoimmune disorder MP:0005351
img increased susceptibility to autoimmune disorder MP:0005350
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img immune system phenotype MP:00053877img autoimmune response MP:0001844
Genes (247)

Species:
human : 247
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED
HumanNLRP10338322NLR family, pyrin domain containing 10
INFERRED
HumanLIN9286826lin-9 homolog (C. elegans)
INFERRED
HumanIL27246778interleukin 27
INFERRED
HumanTIGIT201633T cell immunoreceptor with Ig and ITIM domains
INFERRED
HumanBTLA151888B and T lymphocyte associated
INFERRED
HumanIL23R149233interleukin 23 receptor
INFERRED
HumanCD300LF146722CD300 molecule-like family member f
INFERRED
HumanRASGRP4115727RAS guanyl releasing protein 4
INFERRED
HumanPGLYRP2114770peptidoglycan recognition protein 2
INFERRED
HumanIL17F112744interleukin 17F
INFERRED
HumanIL17RC84818interleukin 17 receptor C
INFERRED
HumanSYVN184447synovial apoptosis inhibitor 1, synoviolin
INFERRED
HumanCD27680381CD276 molecule
INFERRED
HumanPDCD1LG280380programmed cell death 1 ligand 2
INFERRED
HumanVTCN179679V-set domain containing T cell activation inhibitor 1
INFERRED
HumanRNF12879589ring finger protein 128, E3 ubiquitin protein ligase
INFERRED
HumanIL2564806interleukin 25
INFERRED
HumanTPSB264499tryptase beta 2 (gene/pseudogene)
INFERRED
HumanNOD264127nucleotide-binding oligomerization domain containing 2
INFERRED
HumanGPSM363940G-protein signaling modulator 3
INFERRED
HumanIL2159067interleukin 21
INFERRED
HumanENTPD757089ectonucleoside triphosphate diphosphohydrolase 7
INFERRED
HumanLTB4R256413leukotriene B4 receptor 2
INFERRED
HumanHR55806hair growth associated
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002425altered susceptibility to autoimmune disorder0self