Phenodigm > Tissue Phenotype Associations > Tissue Phenotype Association Detail Page

MP ID:
MP:0000438
MP term:
abnormal cranium morphology
Affected anatomical entities (curated):
cranium (MA:0000316)
MA ID MA term Hypergeometric p-val Association rule p-val Supporting mouse genes
MA:0000168 brain 0.000832128 - Sp3, Fgfr3, Slx4, Eya1, Shh, Kdm4b, Cenpj, Psip1, Tbx1, Satb2, Daam2, Itgb1bp1, Sox11, Nsun2, Ube3b, Pax9, Prkg2, Mysm1, Lmna, Gsc, Ndst1, Cbfb, Rgma, Cdk5rap2, Ank, Dlx1, Cdo1, Csrp2bp, Fgfr2, Foxg1, Msx1, Ywhae, Slc25a21, Slc4a4, Phf20, Ctnnb1, Gja1, Apaf1, Smc3, Col1a1, Lrp6, Ids, Npr2, Bmp5, Dusp6, Dlx2
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:0000151 skin - -
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/6ukhjrcw