Phenodigm > Tissue Phenotype Associations > Tissue Phenotype Association Detail Page

MP ID:
MP:0008271
MP term:
abnormal bone ossification
Affected anatomical entities (curated):
MA ID MA term Hypergeometric p-val Association rule p-val Supporting mouse genes
MA:0000145 mammary gland 0.002028005 - Vdr, Bgn, Cthrc1, Mmp14, Twist1, Esr1, Gsk3b, Foxc1, Ednrb, Dnm3os, Tcirg1, Lrp5, Creb3l1, Itgb1bp1, Isg15, Tyrobp, Cdkn1c, Ly6a, Crtap, Klf10, Cebpb, Trps1, Prkcd, Fstl1, Pparg, Hspg2, Fndc3b, Enpp1, Fgfr2, Il6st, Casp3, Ctgf, Nbr1, Ghr, Col1a1, Itgb2, Sqstm1, Papss2, Rps6ka3, Id4, Wwtr1, 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/p7ww67nc