Phenodigm > Tissue Phenotype Associations > Tissue Phenotype Association Detail Page

MP ID:
MP:0005405
MP term:
axon degeneration
Affected anatomical entities (curated):
MA ID MA term Hypergeometric p-val Association rule p-val Supporting mouse genes
MA:0000216 spinal cord 0.000427417 - Pmp22, Abcd2, Uchl1, Nkx6-2, Nefh, Gars, Clcn2, Mag, Scn8a, Stxbp1, Cnp, Kcnj10, Plp1, Lpin1, Galc, Abcd1, Klc1, Aspa, Nefm, Psap
MA:0000168 brain 0.004413020 - Pmp22, Abcd2, Uchl1, Nkx6-2, Nefh, Gars, Clcn2, Opa3, Mag, Scn8a, Stxbp1, Cnp, Kcnj10, Plp1, Mtmr2, Abcd1, Klc1, Aspa, Nefm, Psap
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: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/2dykq9fh