Phenodigm > Tissue Phenotype Associations > Tissue Phenotype Association Detail Page

MP ID:
MP:0001672
MP term:
abnormal embryogenesis/ development
Affected anatomical entities (curated):
MA ID MA term Hypergeometric p-val Association rule p-val Supporting mouse genes
MA:0000337 small intestine 0.001113243 - Yap1, Ppp2ca, Pdpk1, Cdh1, Cttn, Gclc, Hnf4a, Por, Xist, Apex1, Gmnn, Ccna2, Kif22, Acvr1, Slc34a2, Supv3l1, Slc39a4, Pitx2, Prpf19, Dhx9, Ptpn12, Fbxo5, Apob, Cnbp, Itgb1, Slc39a1, Shb, Smad1, Hira, Hsd17b12, Fen1, Fbxl5, Cdk8
MA:0000358 liver 0.003639511 - F3, Yap1, Ppp2ca, Pdpk1, Cdh1, Cttn, Gclc, Hnf4a, Por, Shh, Pten, Xist, Apex1, Gmnn, Kdr, Ccna2, Kif22, Hand1, Bmper, Acvr1, Hhex, Slc34a2, Supv3l1, Slc39a4, Hif1a, Prpf19, Dhx9, Ptpn12, Fbxo5, Apob, Cnbp, Kif11, Itgb1, Slc39a1, Fgfr2, Shb, Smad1, Tpx2, Opa1, Psmg1, Grlf1, Hsd17b12, Fen1, Fbxl5, Cdk8, Bub1b
MA:0000335 colon 0.003664643 - F3, Yap1, Ppp2ca, Pdpk1, Cdh1, Cttn, Hoxd13, Gclc, Hnf4a, Por, Xist, Apex1, Gmnn, Ccna2, Kif22, Acvr1, Slc34a2, Supv3l1, Slc39a4, Pitx2, Hif1a, Prpf19, Dhx9, Shroom3, Ptpn12, Cnbp, Wbp7, Itgb1, Slc39a1, Fgfr2, Smad5, Shb, Smad1, Hira, Grlf1, Hsd17b12, Fen1, Fbxl5, Cdk8, Bub1b
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:0000168 brain - -
MA:0000176 pituitary gland - -
MA:0000216 spinal cord - -
MA:0000261 eye - -
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/en4bzovr