Phenodigm > Tissue Phenotype Associations > Tissue Phenotype Association Detail Page

MP ID:
MP:0011087
MP term:
complete neonatal lethality
Affected anatomical entities (curated):
MA ID MA term Hypergeometric p-val Association rule p-val Supporting mouse genes
MA:0000168 brain 0.000269312 - Sulf2, Magi2, Sp3, Tcf7l2, Prdm16, Fgfr3, Ret, Slc12a5, Sall3, Sdccag8, Sin3b, Nme2, Hdac2, Pitx1, Llgl1, Slc7a1, Eya1, Gsk3b, Atg16l1, Fzd3, Hspb11, Shh, Rfx4, Ednrb, Hdac8, Cntfr, Nr4a2, Fgf9, Cxcr7, Arid1a, Lpcat1, Ssr1, Celsr3, Dgat2, Plod3, Bcl11b, Ecel1, Cacna1c, Tbx1, Snap25, Oat, Carm1, Pip5k1c, Acvr1, Hexim1, Cldn5, Nfe2l1, Grin2b, Ror1, Fkbp8, Sox11, Kif2a, Kif5a, Cask, Fbxo11, Jun, Th, Nbea, Ilf3, Fat1, Nalcn, Zic5, Pax9, Mycbp2, Pdpn, Pds5b, Pax6, Cxcl12, Dgkd, Trps1, Caprin1, Insm1, Grin1, Arx, Cyr61, Krt10, Myh10, Gsc, Ilk, Atp1a2, Fgf18, Ndst1, Scd2, Impad1, Snai2, Cbfb, Lmo4, Col11a1, Fah, Zbtb18, Cadps, Fstl1, Olig2, Elovl4, Phf14, Creb5, Tshz3, Sox2, Hadha, Inpp5e, Ccdc47, Plxnd1, Epas1, Slc17a6, Dhcr7, Snapin, Ece1, Suv420h1, Grb2, Stxbp1, Sox9, Jak1, Atp1a3, Chst11, Gad1, Fgfr2, Lmnb2, Sec23b, Acvr2a, Tshz1, Rspo2, Top2b, Pou3f3, Lrp4, Map1b, Foxg1, Adam17, Msx1, Bag6, Slc18a2, Sema4c, Maf, Ppme1, Nfib, Ctgf, Gja1, Itgav, Madd, Igf1r, Col1a1, Lrp6, Fus, Tubb3, Kit, Kcnq2, Nme1, Atf2, Eif2s1, Bcl11a, Tgfb2, Emx2, Npm1, Gfra1, Vamp2, Fen1, Nr3c1, Lamc1, Ptges3, Tie1, Dscam, Tcf7l1, Pbx3, 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/icy5c80b