Phenodigm > Tissue Phenotype Associations > Tissue Phenotype Association Detail Page

MP ID:
MP:0003861
MP term:
abnormal nervous system development
Affected anatomical entities (curated):
MA ID MA term Hypergeometric p-val Association rule p-val Supporting mouse genes
MA:0000168 brain 0.001574576 - Cnr1, Nr4a2, Nrn1, Aldh1a2, Sox11, Kif2a, Notch1, Phgdh, Amn, Jarid2, Sema3f, Zic2, Gja1, Elavl4, Grlf1
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/qosn0u2x