Phenodigm > Tissue Phenotype Associations > Tissue Phenotype Association Detail Page

MP ID:
MP:0004201
MP term:
fetal growth retardation
Affected anatomical entities (curated):
MA ID MA term Hypergeometric p-val Association rule p-val Supporting mouse genes
MA:0000151 skin 0.004666583 - Sin3b, Sc5d, Rpsa, Eef2, Fst, Irs1, Cul7, Crtap, Stat3, Hsd17b2, Grhl3, Ryr1, Ssr3, Pdgfa, Pik3ca, Gjb2, Psen1, Jarid2, Fgfrl1, Kras, Dhcr7, Mitf, Picalm, Ghr, Nedd4, Mcm4, Birc6, Sav1, Ptges3, Igf2
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: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 - -
* quick link - http://q.sanger.ac.uk/mh50t771