Phenodigm > Tissue Phenotype Associations > Tissue Phenotype Association Detail Page

MP ID:
MP:0005419
MP term:
decreased circulating serum albumin level
Affected anatomical entities (curated):
blood (MA:0000059)
MA ID MA term Hypergeometric p-val Association rule p-val Supporting mouse genes
MA:0000168 brain 0.000000025 - Fam63a, Myl12b, Akap9, St18, Cenpj, Atp5a1, Ube3b, Arid4a, Tnfaip1, Cyb561, Sptbn1, Map2k2, Slc38a10, Slc25a21, Rrm2b, Fam73b, Dbn1, Arhgdia, Rnf7, B2m, Plvap
MA:0000216 spinal cord 0.000001510 - Fam63a, Myl12b, Akap9, St18, Cenpj, Atp5a1, Arid4a, Tnfaip1, Cyb561, Sptbn1, Galnt1, Map2k2, Slc38a10, Rrm2b, Fam73b, Dbn1, Arhgdia, Rnf7, B2m, Plvap, Fcgrt
MA:0000116 adrenal gland 0.000002881 - Fam63a, Myl12b, Akap9, St18, Atp5a1, Cebpa, Ube3b, Tnfaip1, Cyb561, Sptbn1, Galnt1, Map2k2, Slc38a10, Rrm2b, Dbn1, Arhgdia, Rnf7, B2m, Plvap, Fcgrt
MA:0000072 heart 0.000027654 - Fam63a, Myl12b, Akap9, Atp5a1, Cebpa, Ube3b, Arid4a, Tnfaip1, Ada, Cyb561, Sptbn1, Galnt1, Map2k2, Slc38a10, Rrm2b, Fam73b, Arhgdia, Rnf7, B2m, Plvap, Fcgrt
MA:0000176 pituitary gland 0.000117639 - Fam63a, Myl12b, Cd2ap, Akap9, St18, Atp5a1, Arid4a, Tnfaip1, Cyb561, Sptbn1, Galnt1, Map2k2, Slc38a10, Rrm2b, Dbn1, Arhgdia, Rnf7, B2m, Plvap
MA:0000120 pancreas 0.000198620 - Fam63a, Myl12b, Akap9, St18, Atp5a1, Tnfaip1, Cyb561, Sptbn1, Map2k2, Slc38a10, Arhgdia, Rnf7, B2m, Plvap
MA:0000337 small intestine 0.002320001 - Myl12b, Cd2ap, Akap9, Atp5a1, Cebpa, Tnfaip1, Ada, Cyb561, Sptbn1, Galnt1, Slc38a10, Relb, Fam73b, Dbn1, Arhgdia, Rnf7, B2m, Plvap, Fcgrt
MA:0000057 brown adipose tissue - -
MA:0000058 white adipose tissue - -
MA:0000137 peyers patch - -
MA:0000141 spleen - -
MA:0000145 mammary gland - -
MA:0000151 skin - -
MA:0000261 eye - -
MA:0000335 colon - -
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/8nmuasm9