Phenodigm > Tissue Phenotype Associations > Tissue Phenotype Association Detail Page

MP ID:
MP:0002896
MP term:
abnormal bone mineralization
Affected anatomical entities (curated):
MA ID MA term Hypergeometric p-val Association rule p-val Supporting mouse genes
MA:0000145 mammary gland 0.004124008 - Sp3, Sin3b, Slc20a1, Vdr, Mmp14, Cd68, Hoxc10, Nos3, Esr1, Col1a2, Mia3, Cst10, Lrp5, Cav1, Thra, Irs1, Creb3l1, Isg15, Prkar1a, Crtap, Cebpb, Tnfaip1, Lmna, Col11a1, Pth1r, Ank, Hspg2, Mecom, Pex7, Csf1, Sox9, Enpp1, Egr2, Dkk2, Ctnnb1, Col1a1, Spp1, Sqstm1, Rps6ka3, Id4, Acp5, Atf4
MA:0000057 brown adipose tissue - -
MA:0000058 white adipose tissue - -
MA:0000072 heart - -
MA:0000116 adrenal gland - -
MA:0000120 pancreas - -
MA:0000137 peyers patch - -
MA:0000141 spleen - -
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/xddarfdm