Phenodigm > Tissue Phenotype Associations > Tissue Phenotype Association Detail Page

MP ID:
MP:0000913
MP term:
abnormal brain development
Affected anatomical entities (curated):
MA ID MA term Hypergeometric p-val Association rule p-val Supporting mouse genes
MA:0000168 brain 0.000399063 - Lhx1, Pdpk1, Cdh2, Ikbkap, Chd7, Ubr5, Wasf1, Dlc1, Pax6, Kitl, Fbxw7, Ndst1, Lmo4, Rgma, Phgdh, Sptbn1, Kras, Dhcr7, Rapgef2, Zic2, Kcna1, Smad5, Bag6, Plp1, Apaf1, Apc, Hira, Lrp8, Id4, Drd2, Mcph1, Lamc1, Tcf7l1, Gtf2i, Magoh
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/6x4ypz9b