Gene Details



MUT and homologs in 1 species are found in 233 GeneSets:


- Entrez   - GeneNetwork   - Allen Brain Atlas   - Comparative Toxicogenomics Database  

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier I Human GO 741 Genes GS201250: GO:0044429 mitochondrial part
Expand Human 1321 Genes GS219728: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_MEMBRANE
Expand Human 1321 Genes GS219978: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_MEMBRANE
Expand Tier I Human GO 556 Genes GS195139: GO:0055114 oxidation-reduction process
Expand Human 1661 Genes GS219955: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE_PART
Expand Tier I Human GO 1684 Genes GS204629: GO:1901564 organonitrogen compound metabolic process
Expand Human 968 Genes GS219719: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_PLASMA_MEMBRANE
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human 22 Genes GS171433: HP:0003774 End stage renal disease
Expand Tier I Human 124 Genes GS172403: HP:0011873 Abnormal platelet count
Expand Tier I Human CTD 388 Genes GS121370: Clofibrate interacting genes (MeSH:D002994) in CTD
Expand Human 1625 Genes GS221148: http://www.broadinstitute.org/gsea/msigdb/cards/SIGNAL_TRANSDUCTION
Expand Tier I Human 832 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human CTD 4423 Genes GS123718: Ethinyl Estradiol interacting genes (MeSH:D004997) in CTD
Expand Tier I Human 442 Genes GS176801: HP:0001263 Global developmental delay
Expand Tier I Human 36 Genes GS171040: HP:0002157 Azotemia
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 537 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Human 1625 Genes GS221397: http://www.broadinstitute.org/gsea/msigdb/cards/SIGNAL_TRANSDUCTION
Expand Tier I Human 1228 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human GO 139 Genes GS194657: GO:0046906 tetrapyrrole binding
Expand Human 1339 Genes GS219979: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_MEMBRANE
Expand Tier I Human CTD 917 Genes GS121965: Amiodarone interacting genes (MeSH:D000638) in CTD
Expand Tier I Human GO 89 Genes GS200759: GO:0019395 fatty acid oxidation
Expand Tier I Human CTD 866 Genes GS126764: Calcitriol interacting genes (MeSH:D002117) in CTD
Expand Tier I Human 24 Genes GS172745: HP:0010995 Abnormality of dicarboxylic acid metabolism
Expand Tier I Human GO 258 Genes GS197043: GO:0044282 small molecule catabolic process
Expand Tier I Human 16 Genes GS171591: HP:0001969 Tubulointerstitial abnormality
Expand Tier I Human 845 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human 232 Genes GS170999: HP:0000082 Abnormality of renal physiology
Expand Tier I Human 1006 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Human 1661 Genes GS219981: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE_PART
Expand Tier I Human 56 Genes GS173195: HP:0012091 Abnormality of pancreas physiology
Expand Tier I Human CTD 377 Genes GS121976: Zidovudine interacting genes (MeSH:D015215) in CTD
Expand Tier I Human GO 810 Genes GS195897: GO:0044255 cellular lipid metabolic process
Expand Tier I Human 285 Genes GS175119: HP:0001881 Abnormality of leukocytes
Expand Tier I Human GO 5400 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Human GO 186 Genes GS200970: GO:0031406 carboxylic acid binding
Expand Tier I Human 167 Genes GS171201: HP:0001941 Acidosis
Expand Human 1149 Genes GS219725: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE_PART
Expand Human 632 Genes GS219789: http://www.broadinstitute.org/gsea/msigdb/cards/CELL_SURFACE_RECEPTOR_LINKED_SIGNAL_TRANSDUCTION_GO_0007166
Expand Tier I Human 139 Genes GS171000: HP:0000083 Renal insufficiency
Expand Human 1985 Genes GS219980: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human CTD 374 Genes GS124417: Propylthiouracil interacting genes (MeSH:D011441) in CTD
Expand Tier I Human 28 Genes GS171194: HP:0001946 Ketosis
Expand Tier I Human 195 Genes GS174813: HP:0001638 Cardiomyopathy
Expand Tier I Human GO 403 Genes GS199550: GO:0032787 monocarboxylic acid metabolic process
Expand Tier I Human 59 Genes GS176175: HP:0001259 Coma
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human GO 88 Genes GS201124: GO:0009791 post-embryonic development
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human CTD 476 Genes GS125040: Thioacetamide interacting genes (MeSH:D013853) in CTD
Expand Tier I Human GO 5810 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human 33 Genes GS171079: HP:0001882 Leukopenia
Expand Tier I Human GO 4070 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human 148 Genes GS173537: HP:0001872 Abnormality of thrombocytes
Expand Tier I Human GO 2719 Genes GS199273: GO:0043233 organelle lumen
Expand Human 1149 Genes GS219976: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE_PART
Expand Tier I Human 285 Genes GS171902: HP:0010987 Abnormality of cellular immune system
Expand Tier I Human 106 Genes GS171336: HP:0001732 Abnormality of the pancreas
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Human 1661 Genes GS219987: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE_PART
Expand Tier I Human 8 Genes GS172687: HP:0012120 Methylmalonic aciduria
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human GO 147 Genes GS202194: GO:0044242 cellular lipid catabolic process
Expand Tier I Human GO 11 Genes GS202767: GO:0050667 homocysteine metabolic process
Expand Tier I Human GO 1668 Genes GS202188: GO:0044248 cellular catabolic process
Expand Tier I Human 533 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier I Human GO 1852 Genes GS209010: GO:1901575 organic substance catabolic process
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human GO 8 Genes GS207621: GO:0019626 short-chain fatty acid catabolic process
Expand Tier I Human GO 30 Genes GS207747: GO:0046459 short-chain fatty acid metabolic process
Expand Tier I Human CTD 514 Genes GS125959: Cisplatin interacting genes (MeSH:D002945) in CTD
Expand Tier I Human 391 Genes GS175537: HP:0011277 Abnormality of the urinary system physiology
Expand Tier I Human GO 57 Genes GS198222: GO:0006635 fatty acid beta-oxidation
Expand Tier I Human GO 75 Genes GS204133: GO:0009062 fatty acid catabolic process
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Human 1985 Genes GS219986: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human 50 Genes GS171198: HP:0001942 Metabolic acidosis
Expand Tier I Human GO 2673 Genes GS205543: GO:0070013 intracellular organelle lumen
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 1138 Genes GS193812: GO:0006629 lipid metabolic process
Expand Tier I Human GO 102 Genes GS197118: GO:0016597 amino acid binding
Expand Tier I Human CTD 303 Genes GS123351: Omeprazole interacting genes (MeSH:D009853) in CTD
Expand Tier I Human 9 Genes GS172438: HP:0002154 Hyperglycinemia
Expand Tier I Human GO 1 Genes GS206080: GO:0004494 methylmalonyl-CoA mutase activity
Expand Tier I Human 113 Genes GS173647: HP:0012072 Aciduria
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Human 1985 Genes GS219964: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human 105 Genes GS174133: HP:0002013 Vomiting
Expand Tier I Human 2 Genes GS173665: HP:0005979 Metabolic ketoacidosis
Expand Tier I Human 130 Genes GS174137: HP:0002017 Nausea and vomiting
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Human 968 Genes GS219975: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_PLASMA_MEMBRANE
Expand Tier I Human CTD 5075 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Tier I Human GO 198 Genes GS195142: GO:0016054 organic acid catabolic process
Expand Tier I Human 473 Genes GS171893: HP:0011458 Abdominal symptom
Expand Tier I Human 22 Genes GS175380: HP:0003215 Dicarboxylic aciduria
Expand Tier I Human GO 2625 Genes GS196343: GO:0036094 small molecule binding
Expand Tier I Human CTD 281 Genes GS125104: Ethionine interacting genes (MeSH:D005001) in CTD
Expand Tier I Human 43 Genes GS171196: HP:0001944 Dehydration
Expand Tier I Human GO 9 Genes GS205314: GO:0031419 cobalamin binding
Expand Tier I Human 534 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier I Human 104 Genes GS171211: HP:0000091 Abnormality of the renal tubule
Expand Human 1985 Genes GS219747: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 121 Genes GS172672: HP:0004337 Abnormality of amino acid metabolism
Expand Human 1417 Genes GS219730: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Tier I Human 266 Genes GS172415: HP:0002240 Hepatomegaly
Expand Tier I Human GO 339 Genes GS195494: GO:0006520 cellular amino acid metabolic process
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Human 1417 Genes GS219977: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Tier I Human 283 Genes GS172060: HP:0001508 Failure to thrive
Expand Tier I Human 17 Genes GS175827: HP:0010895 Abnormality of glycine metabolism
Expand Human 1625 Genes GS219769: http://www.broadinstitute.org/gsea/msigdb/cards/SIGNAL_TRANSDUCTION
Expand Tier I Human 626 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Human GO 48 Genes GS199797: GO:0072341 modified amino acid binding
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human CTD 132 Genes GS122195: Gentamicins interacting genes (MeSH:D005839) in CTD
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 28 Genes GS199677: GO:0016866 intramolecular transferase activity
Expand Human 1661 Genes GS219738: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE_PART
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 213 Genes GS176040: HP:0011032 Abnormality of fluid regulation
Expand Tier I Human 486 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human 310 Genes GS175805: HP:0003271 Visceromegaly
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 279 Genes GS198219: GO:0006631 fatty acid metabolic process
Expand Human 982 Genes GS219939: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_PLASMA_MEMBRANE
Expand Tier I Human GO 3934 Genes GS198323: GO:0046872 metal ion binding
Expand Tier I Human GO 137 Genes GS205251: GO:0019842 vitamin binding
Expand Tier I Human 268 Genes GS172365: HP:0003110 Abnormality of urine homeostasis
Expand Tier I Human GO 92 Genes GS194937: GO:0034440 lipid oxidation
Expand Tier I Human GO 1518 Genes GS194138: GO:0005739 mitochondrion
Expand Tier I Human GO 2764 Genes GS194555: GO:0031974 membrane-enclosed lumen
Expand Tier I Human GO 136 Genes GS203419: GO:0016853 isomerase activity
Expand Tier I Human GO 234 Genes GS209234: GO:0006790 sulfur compound metabolic process
Expand Tier I Human GO 846 Genes GS204326: GO:0019752 carboxylic acid metabolic process
Expand Tier I Human GO 89 Genes GS208495: GO:0072329 monocarboxylic acid catabolic process
Expand Tier I Human 545 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human 26 Genes GS176059: HP:0002134 Abnormality of the basal ganglia
Expand Tier I Human GO 2392 Genes GS206737: GO:0043168 anion binding
Expand Tier I Human GO 1993 Genes GS207862: GO:0009056 catabolic process
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 5962 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human 215 Genes GS172139: HP:0010993 Abnormality of the cerebral subcortex
Expand Human 1321 Genes GS219945: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_MEMBRANE
Expand Tier I Human 84 Genes GS170815: HP:0011400 Abnormal CNS myelination
Expand Tier I Human 394 Genes GS172362: HP:0004325 Decreased body weight
Expand Tier I Human GO 953 Genes GS202555: GO:0043436 oxoacid metabolic process
Expand Human 1321 Genes GS219984: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_MEMBRANE
Expand Tier I Human 737 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human 121 Genes GS173538: HP:0001873 Thrombocytopenia
Expand Tier I Human CTD 281 Genes GS121771: Benzbromarone interacting genes (MeSH:D001553) in CTD
Expand Tier I Human 456 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Human CTD 1522 Genes GS124579: Selenium interacting genes (MeSH:D012643) in CTD
Expand Tier I Human 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human GO 145 Genes GS209189: GO:0030258 lipid modification
Expand Tier I Human 134 Genes GS175172: HP:0004354 Abnormality of carboxylic acid metabolism
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human CTD 4389 Genes GS123768: Cyclosporine interacting genes (MeSH:D016572) in CTD
Expand Tier I Human CTD 5725 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
Expand Tier I Human 10 Genes GS175922: HP:0004341 Abnormality of the vitamin B12 metabolism
Expand Human 1339 Genes GS219948: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_MEMBRANE
Expand Tier I Human 200 Genes GS174812: HP:0001637 Abnormality of the myocardium
Expand Tier I Human 17 Genes GS174763: HP:0010894 Abnormality of serine family amino acid metabolism
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 607 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human 71 Genes GS176168: HP:0001254 Lethargy
Expand Tier I Human GO 8702 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 990 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Human 8 Genes GS173829: HP:0002912 Methylmalonic acidemia
Expand Tier I Human GO 278 Genes GS194621: GO:0005759 mitochondrial matrix
Expand Tier I Human GO 42 Genes GS196745: GO:0000096 sulfur amino acid metabolic process
Expand Human 982 Genes GS219722: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_PLASMA_MEMBRANE
Expand Human 1417 Genes GS219983: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Human 632 Genes GS221149: http://www.broadinstitute.org/gsea/msigdb/cards/CELL_SURFACE_RECEPTOR_LINKED_SIGNAL_TRANSDUCTION_GO_0007166
Expand Human 1339 Genes GS219985: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_MEMBRANE
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human GO 4034 Genes GS208978: GO:0043169 cation binding
Expand Tier I Human 487 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier I Human CTD 17 Genes GS127074: antibiotic G 418 interacting genes (MeSH:C010680) in CTD
Expand Tier I Human 11 Genes GS175925: HP:0004340 Abnormality of vitamin B metabolism
Expand Human 632 Genes GS221398: http://www.broadinstitute.org/gsea/msigdb/cards/CELL_SURFACE_RECEPTOR_LINKED_SIGNAL_TRANSDUCTION_GO_0007166
Expand Tier I Human 25 Genes GS174393: HP:0001733 Pancreatitis
Expand Tier I Human GO 198 Genes GS200384: GO:0046395 carboxylic acid catabolic process
Expand Tier I Human GO 971 Genes GS210163: GO:0006082 organic acid metabolic process
Expand Tier I Human 29 Genes GS172066: HP:0001987 Hyperammonemia
Expand Tier I Human GO 5321 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Human CTD 1551 Genes GS125506: Valproic Acid interacting genes (MeSH:D014635) in CTD
Expand Tier I Human 182 Genes GS173028: HP:0004360 Abnormality of acid-base homeostasis
Expand Tier I Human 2 Genes GS171500: HP:0002453 Abnormality of the globus pallidus
Expand Human 1339 Genes GS219731: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_MEMBRANE
Expand Tier I Human 8 Genes GS172184: HP:0002188 Delayed CNS myelination
Expand Tier I Human GO 259 Genes GS202414: GO:0044712 single-organism catabolic process
Expand Human 968 Genes GS219936: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_PLASMA_MEMBRANE
Expand Tier I Human GO 4567 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human CTD 3 Genes GS125099: adefovir interacting genes (MeSH:C053001) in CTD
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human 534 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier I Human GO 6769 Genes GS210002: GO:0044444 cytoplasmic part
Expand Human 968 Genes GS221018: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_PLASMA_MEMBRANE
Expand Tier I Human 5 Genes GS172160: HP:0001970 Tubulointerstitial nephritis
Expand Human 968 Genes GS221267: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_PLASMA_MEMBRANE
Expand Tier I Human 128 Genes GS173093: HP:0004372 Reduced consciousness/confusion
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 680 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human GO 252 Genes GS194309: GO:0016042 lipid catabolic process
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Human 1149 Genes GS219982: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE_PART
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human 12 Genes GS172158: HP:0100508 Abnormality of vitamin metabolism
Expand Tier I Human 13 Genes GS172302: HP:0001993 Ketoacidosis
Expand Tier I Human GO 2511 Genes GS207903: GO:0044281 small molecule metabolic process
Expand Tier I Human GO 6278 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human 37 Genes GS173012: HP:0004364 Abnormality of nitrogen compound homeostasis
Expand Tier I Human 57 Genes GS171016: HP:0011893 Abnormal leukocyte count
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Human 1417 Genes GS219947: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Human 1149 Genes GS219942: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE_PART
Expand Human 1625 Genes GS222093: http://www.broadinstitute.org/gsea/msigdb/cards/SIGNAL_TRANSDUCTION
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 197 Genes GS204383: GO:0006575 cellular modified amino acid metabolic process
Expand Tier I Human GO 5452 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Human 22 Genes GS173015: HP:0003112 Abnormality of serum amino acid levels