Phenodigm > Tissue Phenotype Associations > Tissue Phenotype Association Detail Page

MP ID:
MP:0001325
MP term:
abnormal retina morphology
Affected anatomical entities (curated):
retina (MA:0000276)
MA ID MA term Hypergeometric p-val Association rule p-val Supporting mouse genes
MA:0000261 eye 0.000000692 - Prdm16, Ccnd1, Fscn2, Rp1l1, Crx, Tulp1, Aldh1a3, Rdh10, Rom1, Vsx2, Marcksl1, Tfap2a, Spns2, Srsf4, Oat, Hps1, Col4a1, Fbxo11, Rpe65, Cdkn1c, Pde6b, Mpp4, Six6, Rho, Grhl3, Bbs4, Rorb, Myh10, Elovl4, Unc119, Ctsd, Arhgap25, Cdhr1, Mab21l1, Itgb5, Rs1, Pou4f2, Pfdn5, Slc38a10, Rbp1, Adam17, Mitf, Crb1, Sema3e, Clk1, Grip1, Cep290, Cabp4, Prom1, Rpgrip1, Guca1a, Fat3, Lhx2
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/6rrgqgek