Phenodigm > Tissue Phenotype Associations > Tissue Phenotype Association Detail Page

MP ID:
MP:0002113
MP term:
abnormal skeleton development
Affected anatomical entities (curated):
MA ID MA term Hypergeometric p-val Association rule p-val Supporting mouse genes
MA:0000151 skin 0.001712257 - Mmp14, Esr1, Ostm1, Foxc1, Msx2, Twsg1, Tgfbr3, Lepr, Tbx15, Cdkn1c, Kitl, Plekho1, Col5a2, Fgf18, Cbfb, Pth1r, Sox9, Prkaca, Egr2, Rxra, Tnfrsf11b, Casp3, Lep, Ghr, Npr2, Papss2, Acp5, Igf2
MA:0000072 heart - -
MA:0000116 adrenal gland - -
MA:0000120 pancreas - -
MA:0000137 peyers patch - -
MA:0000141 spleen - -
MA:0000145 mammary gland - -
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 - -
MA:0000057 brown adipose tissue - -
MA:0000058 white adipose tissue - -
* quick link - http://q.sanger.ac.uk/e1ytbv03