Phenodigm > Tissue Phenotype Associations > Tissue Phenotype Association Detail Page

MP ID:
MP:0001326
MP term:
retinal degeneration
Affected anatomical entities (curated):
retina (MA:0000276)
MA ID MA term Hypergeometric p-val Association rule p-val Supporting mouse genes
MA:0000261 eye 0.000006298 - Rras2, Gngt1, Aipl1, Fscn2, Clcn3, Tulp1, Rom1, Apoe, Lpcat1, Polg2, Slc1a3, Oat, Mdm1, Rpe65, Prpf8, Pde6b, Rho, Pde6a, Bbs4, Rorb, Chsy1, Bbs1, Ttc8, Unc119, Cdhr1, Pin1, Mitf, Gnat1, Crb1, Cep290, Atp1b2, Sparc, Rlbp1
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/56k0iosd