Phenodigm > Tissue Phenotype Associations > Tissue Phenotype Association Detail Page

MP ID:
MP:0004816
MP term:
abnormal class switch recombination
Affected anatomical entities (curated):
MA ID MA term Hypergeometric p-val Association rule p-val Supporting mouse genes
MA:0000141 spleen 0.000070439 - Nfkbid, Il2rg, Vav2, Cd37, Cd79a, Ruvbl2, Map3k14, Lta, Bach2, H2afx, Fli1, Ltb, Batf, Cd3e, Swap70, Stat6, Ighg1, Ccr7, Lyn, Nfkb1, Tnfrsf13b, Icos, Irf4, Bcl3, Cr2
MA:0000058 white adipose tissue 0.000164147 - Il2rg, Esr1, Cd37, Cd79a, Ruvbl2, Bach2, Fli1, Ltb, Cd3e, Swap70, Stat6, Ighg1, Ccr7, Lyn, Nfkb1, Tnfrsf13b, Icos, Bcl3, Cr2
MA:0000057 brown adipose tissue - -
MA:0000072 heart - -
MA:0000116 adrenal gland - -
MA:0000120 pancreas - -
MA:0000137 peyers patch - -
MA:0000145 mammary gland - -
MA:0000151 skin - -
MA:0000168 brain - -
MA:0000176 pituitary gland - -
MA:0000216 spinal cord - -
MA:0000261 eye - -
MA:0000335 colon - -
MA:0000337 small intestine - -
MA:0000358 liver - -
MA:0000389 uterus - -
MA:0000404 prostate gland - -
MA:0000411 testis - -
MA:0000415 lung - -
MA:0002439 skeletal muscle tissue - -
* quick link - http://q.sanger.ac.uk/el85clfo