Phenodigm > Tissue Phenotype Associations > Tissue Phenotype Association Detail Page

MP ID:
MP:0005551
MP term:
abnormal eye electrophysiology
Affected anatomical entities (curated):
MA ID MA term Hypergeometric p-val Association rule p-val Supporting mouse genes
MA:0000261 eye 0.000000000 - Ccnd1, Gngt1, Aipl1, Fscn2, Clcn3, Fos, Plin2, Crx, Rdh12, Rom1, Asic3, Apoe, Lpcat1, Lrat, Cplx4, C3, Slc1a3, Oat, Mdm1, Rpe65, Dmd, Pde6b, Rbp3, Drd1a, Rho, Rd3, Pde6a, Dnase2b, Bbs4, Bbs1, Elovl4, Unc119, Pde6c, Rcvrn, Cdhr1, Cplx3, Pde6g, Rs1, Pou4f2, Pfdn5, Rbp1, Gnat1, Cacna1f, Rgr, Cabp4, Sod1, Cacna2d4, Rdh5, Guca1a, Drd4, Gnb3
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: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/6au2ewzd