Gene Details



PAH and homologs in 6 species are found in 455 GeneSets:


- Entrez   - Ensembl   - GeneNetwork   - STRING   - 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 Mouse MP 1350 Genes GS165707: MP:0000428 abnormal craniofacial morphology
Expand Tier I Mouse GO 1 Genes GS189706: GO:0006571 tyrosine biosynthetic process
Expand Tier I Mouse 537 Genes GS136454: postnatal body weight growth 16 (Pbwg16, Published QTL Chr 10)
Expand Tier III Mouse 2551 Genes GS866: Linear decrease in expression in both Pax6 (Sey) mutants and controls.
Expand Tier I Mouse GO 5650 Genes GS183848: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 17 Genes GS173032: HP:0007513 Generalized hypopigmentation
Expand Human 169 Genes GS219782: http://www.broadinstitute.org/gsea/msigdb/cards/CARBOXYLIC_ACID_METABOLIC_PROCESS
Expand Tier I Human 14 Genes GS172131: HP:0000635 Blue irides
Expand Tier I Human 882 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human GO 1684 Genes GS204629: GO:1901564 organonitrogen compound metabolic process
Expand Tier I Mouse 558 Genes GS135258: anti-erythrocyte autoantibody modifier 3 (Aem3, Published QTL Chr 10)
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Mouse 515 Genes GS135860: femur breaking strength 3 (Fembrs3, Published QTL Chr 10)
Expand Tier I Mouse 527 Genes GS136720: susceptibility to lung cancer 22 (Sluc22, Published QTL Chr 10)
Expand Tier I Human 41 Genes GS171926: HP:0007018 Attention deficit hyperactivity disorder
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Mouse GO 2260 Genes GS189855: GO:0043168 anion binding
Expand Tier I Mouse GO 8 Genes GS178920: GO:0006558 L-phenylalanine metabolic process
Expand Tier I Mouse 558 Genes GS135645: cardiac modifier of nmd 2 (Cmn2, Published QTL Chr 10)
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Mouse MP 183 Genes GS167630: MP:0000947 convulsive seizures
Expand Tier I Mouse GO 1822 Genes GS190997: GO:0044281 small molecule metabolic process
Expand Tier I Mouse GO 3537 Genes GS192041: GO:0043169 cation binding
Expand Tier I Human 94 Genes GS173846: HP:0003355 Aminoaciduria
Expand Tier I Human GO 434 Genes GS202416: GO:0044711 single-organism biosynthetic process
Expand Tier I Human 170 Genes GS174488: HP:0000525 Abnormality of the iris
Expand Tier I Mouse 537 Genes GS136079: juvenile cystic kidney modifier 1 (Jckm1, Published QTL Chr 10)
Expand Tier I Mouse GO 919 Genes GS178388: GO:0055114 oxidation-reduction process
Expand Tier I Human CTD 2424 Genes GS123265: Estradiol interacting genes (MeSH:D004958) in CTD
Expand Tier I Mouse GO 2223 Genes GS179830: GO:0006464 cellular protein modification process
Expand Tier I Mouse 406 Genes GS136249: mean corpuscular hemoglobin QTL 1 (Mchq1, Published QTL Chr 10)
Expand Tier I Mouse 515 Genes GS136052: IGF-1 serum levels 2 (Igf1sl2, Published QTL Chr 10)
Expand Tier I Mouse GO 4887 Genes GS188190: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human GO 2507 Genes GS196934: GO:0065008 regulation of biological quality
Expand Tier I Mouse 535 Genes GS135450: bone length and organs 6 (Bod6, Published QTL Chr 10)
Expand Tier I Human GO 566 Genes GS194646: GO:0042803 protein homodimerization activity
Expand Tier I Human GO 15 Genes GS210196: GO:0042423 catecholamine biosynthetic process
Expand Tier I Mouse GO 26 Genes GS189596: GO:0042558 pteridine-containing compound metabolic process
Expand Tier I Mouse GO 385 Genes GS185586: GO:0044711 single-organism biosynthetic process
Expand Tier I Human 1 Genes GS172504: HP:0004920 Phenylpyruvic acidemia
Expand Tier I Human 34 Genes GS174840: HP:0011358 Generalized hypopigmentation of hair
Expand Tier I Human GO 1099 Genes GS195083: GO:0007267 cell-cell signaling
Expand Human 132 Genes GS220917: http://www.broadinstitute.org/gsea/msigdb/cards/AMINE_METABOLIC_PROCESS
Expand Tier I Human 491 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Mouse MP 343 Genes GS166753: MP:0001935 decreased litter size
Expand Tier I Mouse GO 24 Genes GS183029: GO:0009072 aromatic amino acid family metabolic process
Expand Tier I Mouse GO 735 Genes GS181962: GO:0016491 oxidoreductase activity
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Mouse MP 214 Genes GS167898: MP:0009357 abnormal seizure response to inducing agent
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 786 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 80 Genes GS172801: HP:0000752 Hyperactivity
Expand Tier I Human GO 5223 Genes GS207857: GO:0009058 biosynthetic process
Expand Tier I Human GO 713 Genes GS204630: GO:1901565 organonitrogen compound catabolic process
Expand Tier I Mouse MP 648 Genes GS168389: MP:0001186 pigmentation phenotype
Expand Tier I Mouse GO 717 Genes GS185724: GO:0043436 oxoacid metabolic process
Expand Human 171 Genes GS219779: http://www.broadinstitute.org/gsea/msigdb/cards/ORGANIC_ACID_METABOLIC_PROCESS
Expand Tier I Mouse 535 Genes GS136650: skeletal size (tail length) 4 (Skl4, Published QTL Chr 10)
Expand Tier I Mouse MP 3019 Genes GS165466: MP:0003632 abnormal nervous system morphology
Expand Tier I Mouse MP 73 Genes GS170587: MP:0005408 hypopigmentation
Expand Tier I Mouse MP 2057 Genes GS169835: MP:0005389 reproductive system phenotype
Expand Tier I Mouse MP 28 Genes GS167519: MP:0002802 abnormal discrimination learning
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human CTD 2013 Genes GS126646: Carbon Tetrachloride interacting genes (MeSH:D002251) in CTD
Expand Tier I Mouse 500 Genes GS136165: leishmaniasis resistance 19 (Lmr19, Published QTL Chr 10)
Expand Tier I Human GO 2464 Genes GS196595: GO:0006464 cellular protein modification process
Expand Human 69 Genes GS221129: http://www.broadinstitute.org/gsea/msigdb/cards/AMINO_ACID_METABOLIC_PROCESS
Expand Tier I Mouse 558 Genes GS135790: epilepsy 3 (El3, Published QTL Chr 10)
Expand Tier I Human 473 Genes GS171893: HP:0011458 Abdominal symptom
Expand Tier I Mouse GO 3548 Genes GS184566: GO:0019538 protein metabolic process
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 739 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human GO 339 Genes GS195494: GO:0006520 cellular amino acid metabolic process
Expand Tier I Mouse MP 378 Genes GS167214: MP:0005319 abnormal enzyme/ coenzyme level
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human GO 1 Genes GS209728: GO:0009095 aromatic amino acid family biosynthetic process, prephenate pathway
Expand Tier I Mouse 536 Genes GS135751: experimental allergic encephalomyelitis susceptibility 17 (Eae17, Published QTL Chr 10)
Expand Tier I Human 1 Genes GS175609: HP:0005982 Reduced phenylalanine hydroxylase activity
Expand Tier I Mouse GO 3442 Genes GS181533: GO:0046872 metal ion binding
Expand Tier I Human GO 42 Genes GS198210: GO:0006584 catecholamine metabolic process
Expand Tier I Mouse 493 Genes GS136910: vertebral morphology and mechanical traits 15 (Vmmt15, Published QTL Chr 10)
Expand Tier I Mouse MP 1350 Genes GS165228: MP:0005382 craniofacial phenotype
Expand Tier I Mouse MP 169 Genes GS165461: MP:0001525 impaired balance
Expand Tier I Human 48 Genes GS176364: HP:0008034 Abnormal iris pigmentation
Expand Tier I Mouse GO 195 Genes GS182519: GO:0006732 coenzyme metabolic process
Expand Tier I Human 140 Genes GS174860: HP:0010549 Paralysis due to lesions of the principle motor tracts
Expand Tier I Mouse GO 691 Genes GS177311: GO:1901361 organic cyclic compound catabolic process
Expand Tier I Mouse MP 1082 Genes GS166660: MP:0001731 abnormal postnatal growth
Expand Tier II Mouse 526 Genes GS84243: METH responses for home cage activity (Published QTL, Chr 10)
Expand Tier I Mouse MP 985 Genes GS167025: MP:0003953 abnormal hormone level
Expand Tier I Mouse MP 814 Genes GS163226: MP:0003312 abnormal locomotor coordination
Expand Tier I Mouse GO 4114 Genes GS193414: GO:0044249 cellular biosynthetic process
Expand Tier I Human 344 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human 453 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Human GO 953 Genes GS202555: GO:0043436 oxoacid metabolic process
Expand Tier I Human GO 168 Genes GS197078: GO:0005506 iron ion binding
Expand Human 9 Genes GS220143: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PHENYLALANINE_METABOLISM
Expand Tier I Mouse GO 106 Genes GS180335: GO:0016597 amino acid binding
Expand Tier I Human 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Mouse 546 Genes GS135360: B.burgdorferi-associated arthritis 18 (Bbaa18, Published QTL Chr 10)
Expand Tier I Mouse MP 23 Genes GS167218: MP:0001496 audiogenic seizures
Expand Tier I Mouse GO 1518 Genes GS192074: GO:1901575 organic substance catabolic process
Expand Human 9 Genes GS219643: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PHENYLALANINE_METABOLISM
Expand Tier I Mouse GO 8414 Genes GS185585: GO:0044710 single-organism metabolic process
Expand Tier I Human 123 Genes GS173242: HP:0001337 Tremor
Expand Tier I Human 39 Genes GS174016: HP:0000717 Autism
Expand Tier I Mouse 531 Genes GS135778: endothelin receptor type B modifier 1 (Ednrbm1, Published QTL Chr 10)
Expand Tier I Human GO 4034 Genes GS208978: GO:0043169 cation binding
Expand Tier I Human GO 42 Genes GS199601: GO:0034311 diol metabolic process
Expand Tier I Human 56 Genes GS175220: HP:0009887 Abnormality of hair pigmentation
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human 117 Genes GS170989: HP:0010766 Ectopic calcification
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Mouse 537 Genes GS136122: life span 2 (Lifespan2, Published QTL Chr 10)
Expand Tier I Human GO 105 Genes GS204132: GO:0009063 cellular amino acid catabolic process
Expand Tier I Human 319 Genes GS176591: HP:0001276 Hypertonia
Expand Tier I Mouse 536 Genes GS136154: limb length QTL 4 (Lmblgq4, Published QTL Chr 10)
Expand Tier I Human GO 3 Genes GS196451: GO:0004505 phenylalanine 4-monooxygenase activity
Expand Tier I Mouse MP 186 Genes GS167222: MP:0005311 abnormal circulating amino acid level
Expand Tier I Mouse 515 Genes GS135323: apomorphine stress induced climbing 3 (Apsic3, Published QTL Chr 10)
Expand Tier I Human GO 3885 Genes GS201367: GO:0019538 protein metabolic process
Expand Tier II Mouse 34 Genes GS36417: Whole Brain Gene expression correlates of Open Field - Total rears 5-10 minutes in Males BXD
Expand Human 69 Genes GS221378: http://www.broadinstitute.org/gsea/msigdb/cards/AMINO_ACID_METABOLIC_PROCESS
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human GO 14 Genes GS205552: GO:0042136 neurotransmitter biosynthetic process
Expand Tier I Human GO 751 Genes GS202715: GO:0035637 multicellular organismal signaling
Expand Tier I Mouse MP 3543 Genes GS169828: MP:0005386 behavior/neurological phenotype
Expand Tier I Mouse 530 Genes GS136631: small effect CIA locus 5 (Secia5, Published QTL Chr 10)
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human GO 9 Genes GS195676: GO:0006558 L-phenylalanine metabolic process
Expand Tier I Human GO 2511 Genes GS207903: GO:0044281 small molecule metabolic process
Expand Tier I Human 123 Genes GS176672: HP:0000980 Pallor
Expand Tier I Mouse MP 1083 Genes GS167755: MP:0000783 abnormal forebrain morphology
Expand Tier I Mouse GO 6 Genes GS178921: GO:0006559 L-phenylalanine catabolic process
Expand Tier I Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Human 69 Genes GS219804: http://www.broadinstitute.org/gsea/msigdb/cards/AMINO_ACID_METABOLIC_PROCESS
Expand Tier I Human 60 Genes GS174300: HP:0000718 Aggressive behavior
Expand Tier I Mouse GO 4500 Genes GS186790: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Mouse GO 5225 Genes GS189860: GO:0043167 ion binding
Expand Tier I Mouse GO 6 Genes GS179652: GO:0018126 protein hydroxylation
Expand Tier I Human 177 Genes GS173540: HP:0002115 Sparse or absent hair
Expand Tier I Human GO 9 Genes GS195677: GO:0006559 L-phenylalanine catabolic process
Expand Tier I Human GO 186 Genes GS200970: GO:0031406 carboxylic acid binding
Expand Tier I Mouse GO 49 Genes GS191315: GO:0008652 cellular amino acid biosynthetic process
Expand Tier I Human 39 Genes GS174048: HP:0000729 Autism spectrum disorder
Expand Tier I Mouse MP 3716 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier I Human GO 5810 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human 358 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Mouse 537 Genes GS136004: hepatocarcinogen resistance 2 (Hpcr2, Published QTL Chr 10)
Expand Tier I Mouse 558 Genes GS135312: aortic lesion size 1 (Aorls1, Published QTL Chr 10)
Expand Tier I Mouse MP 956 Genes GS168336: MP:0000367 abnormal coat/ hair morphology
Expand Tier I Mouse GO 154 Genes GS180298: GO:0005506 iron ion binding
Expand Tier I Human GO 651 Genes GS195082: GO:0007268 synaptic transmission
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 Mouse MP 2406 Genes GS169391: MP:0002066 abnormal motor capabilities/coordination/movement
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Mouse MP 898 Genes GS169390: MP:0002067 abnormal sensory capabilities/reflexes/nociception
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human GO 7 Genes GS196821: GO:0016714 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced pteridine as one donor, and incorporation of one atom of oxygen
Expand Human 92 Genes GS220919: http://www.broadinstitute.org/gsea/msigdb/cards/AMINO_ACID_AND_DERIVATIVE_METABOLIC_PROCESS
Expand Tier I Human 699 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human 544 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Mouse GO 10879 Genes GS181473: GO:0005488 binding
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Mouse MP 497 Genes GS168996: MP:0009643 abnormal urine homeostasis
Expand Tier I Human GO 215 Genes GS199314: GO:0006732 coenzyme metabolic process
Expand Tier I Human GO 8622 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Mouse MP 797 Genes GS168155: MP:0005502 abnormal renal/urinary system physiology
Expand Tier I Mouse GO 5103 Genes GS192512: GO:0003824 catalytic activity
Expand Tier I Human 7 Genes GS174964: HP:0010893 Abnormality of phenylalanine metabolism
Expand Tier I Human CTD 129 Genes GS124163: Streptozocin interacting genes (MeSH:D013311) in CTD
Expand Tier I Mouse GO 254 Genes GS185538: GO:0048037 cofactor binding
Expand Tier I Human 130 Genes GS174137: HP:0002017 Nausea and vomiting
Expand Tier I Human GO 198 Genes GS195142: GO:0016054 organic acid catabolic process
Expand Tier I Mouse GO 235 Genes GS178395: GO:0016053 organic acid biosynthetic process
Expand Tier I Mouse GO 673 Genes GS181666: GO:0019439 aromatic compound catabolic process
Expand Tier I Human GO 422 Genes GS207919: GO:0044283 small molecule biosynthetic process
Expand Tier I Human 121 Genes GS172672: HP:0004337 Abnormality of amino acid metabolism
Expand Tier I Human GO 10 Genes GS206582: GO:0006570 tyrosine metabolic process
Expand Tier I Mouse MP 3437 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 709 Genes GS198755: GO:0016491 oxidoreductase activity
Expand Tier I Human GO 3626 Genes GS198456: GO:0019438 aromatic compound biosynthetic process
Expand Tier I Mouse GO 675 Genes GS187462: GO:0019752 carboxylic acid metabolic process
Expand Tier I Human GO 19 Genes GS199826: GO:0009074 aromatic amino acid family catabolic process
Expand Tier I Mouse MP 12 Genes GS167300: MP:0001460 abnormal olfactory -discrimination memory
Expand Tier I Mouse GO 2907 Genes GS181667: GO:0019438 aromatic compound biosynthetic process
Expand Tier III Rat 3441 Genes GS135132: bHR vs bLR genes different in Nucleus Acumbens
Expand Tier I Mouse GO 373 Genes GS191013: GO:0044283 small molecule biosynthetic process
Expand Tier I Mouse MP 88 Genes GS163714: MP:0000433 microcephaly
Expand Tier I Human GO 4593 Genes GS206355: GO:0023052 signaling
Expand Tier I Mouse MP 4173 Genes GS165527: MP:0005378 growth/size phenotype
Expand Tier I Human 177 Genes GS175431: HP:0011122 Abnormality of skin physiology
Expand Tier I Human CTD 1291 Genes GS125402: Diethylnitrosamine interacting genes (MeSH:D004052) in CTD
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human 17 Genes GS173405: HP:0002686 Prenatal maternal abnormality
Expand Tier I Human GO 3934 Genes GS198323: GO:0046872 metal ion binding
Expand Tier III Rat 3441 Genes GS135133: bHR vs bLR genes different in Hippocampus
Expand Tier I Human 268 Genes GS172365: HP:0003110 Abnormality of urine homeostasis
Expand Tier I Human GO 4719 Genes GS195977: GO:0007154 cell communication
Expand Tier I Mouse GO 2 Genes GS183030: GO:0009073 aromatic amino acid family biosynthetic process
Expand Tier II Mouse 528 Genes GS84242: ethanol withdrawal (Published QTL, Chr 10)
Expand Human 9 Genes GS220989: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PHENYLALANINE_METABOLISM
Expand Tier I Mouse MP 462 Genes GS169393: MP:0002064 seizures
Expand Tier I Mouse GO 933 Genes GS178813: GO:0046983 protein dimerization activity
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 793 Genes GS198455: GO:0019439 aromatic compound catabolic process
Expand Tier I Human GO 7311 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human GO 5047 Genes GS210357: GO:0044249 cellular biosynthetic process
Expand Tier I Mouse GO 7552 Genes GS180452: GO:0044237 cellular metabolic process
Expand Tier I Human 203 Genes GS174706: HP:0000553 Abnormality of the uvea
Expand Tier I Mouse 531 Genes GS136147: lithogenic gene 7 (Lith7, Published QTL Chr 10)
Expand Tier I Human GO 969 Genes GS195570: GO:0046983 protein dimerization activity
Expand Human 171 Genes GS220915: http://www.broadinstitute.org/gsea/msigdb/cards/ORGANIC_ACID_METABOLIC_PROCESS
Expand Tier I Mouse 536 Genes GS135339: atherosclerosis 17 (Ath17, Published QTL Chr 10)
Expand Tier I Mouse GO 2303 Genes GS177598: GO:0043412 macromolecule modification
Expand Tier I Mouse MP 1316 Genes GS165798: MP:0005367 renal/urinary system phenotype
Expand Tier I Mouse GO 3 Genes GS179692: GO:0004505 phenylalanine 4-monooxygenase activity
Expand Tier I Human 102 Genes GS173545: HP:0010647 Abnormal elasticity of skin
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 Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Mouse GO 215 Genes GS178736: GO:0006520 cellular amino acid metabolic process
Expand Tier I Mouse MP 1485 Genes GS166712: MP:0002161 abnormal fertility/fecundity
Expand Tier I Mouse MP 2663 Genes GS168995: MP:0009642 abnormal blood homeostasis
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Mouse GO 6435 Genes GS177531: GO:0043170 macromolecule metabolic process
Expand Tier I Human 607 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human GO 26 Genes GS205549: GO:0042133 neurotransmitter metabolic process
Expand Tier I Human GO 15 Genes GS199604: GO:0034312 diol biosynthetic process
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 II Mouse 70 Genes GS36372: Whole Brain Gene expression correlates of Open Field - Total rears 0-5 minutes in Males BXD
Expand Tier I Mouse GO 197 Genes GS185584: GO:0044712 single-organism catabolic process
Expand Tier I Mouse MP 363 Genes GS167748: MP:0000788 abnormal cerebral cortex morphology
Expand Tier I Mouse GO 1411 Genes GS187769: GO:1901564 organonitrogen compound metabolic process
Expand Tier I Human GO 29 Genes GS199831: GO:0009072 aromatic amino acid family metabolic process
Expand Tier I Human CTD 1760 Genes GS123048: Tretinoin interacting genes (MeSH:D014212) in CTD
Expand Tier I Mouse GO 2223 Genes GS182234: GO:0036211 protein modification process
Expand Tier I Human 32 Genes GS176416: HP:0100679 Lack of skin elasticity
Expand Tier I Human GO 257 Genes GS194434: GO:0051186 cofactor metabolic process
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Mouse GO 235 Genes GS183584: GO:0046394 carboxylic acid biosynthetic process
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human GO 5369 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Human 92 Genes GS219805: http://www.broadinstitute.org/gsea/msigdb/cards/AMINO_ACID_AND_DERIVATIVE_METABOLIC_PROCESS
Expand Tier I Mouse 537 Genes GS136778: systolic blood pressure 1 (Sysbp1, Published QTL Chr 10)
Expand Tier I Mouse 569 Genes GS135500: brain size control 1 (Bsc1, Published QTL Chr 10)
Expand Tier I Human 59 Genes GS175262: HP:0000964 Eczema
Expand Tier I Mouse GO 4218 Genes GS192073: GO:1901576 organic substance biosynthetic process
Expand Tier I Human GO 971 Genes GS210163: GO:0006082 organic acid metabolic process
Expand Tier I Mouse MP 2200 Genes GS165465: MP:0003633 abnormal nervous system physiology
Expand Tier I Mouse GO 189 Genes GS184168: GO:0031406 carboxylic acid binding
Expand Tier I Mouse GO 7644 Genes GS188399: GO:0044238 primary metabolic process
Expand Tier I Mouse GO 1648 Genes GS190954: GO:0009056 catabolic process
Expand Tier I Mouse MP 73 Genes GS166915: MP:0005322 abnormal serotonin level
Expand Tier I Human 567 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human GO 5321 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Mouse MP 360 Genes GS163635: MP:0001933 abnormal litter size
Expand Tier I Mouse GO 8072 Genes GS184218: GO:0071704 organic substance metabolic process
Expand Tier I Human GO 3254 Genes GS200602: GO:0044267 cellular protein metabolic process
Expand Tier I Mouse GO 4478 Genes GS184435: GO:0046483 heterocycle metabolic process
Expand Tier I Human GO 259 Genes GS202414: GO:0044712 single-organism catabolic process
Expand Tier I Human GO 3737 Genes GS194038: GO:1901362 organic cyclic compound biosynthetic process
Expand Tier I Human 10 Genes GS174749: HP:0004338 Abnormality of aromatic amino acid family metabolism
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Mouse MP 1302 Genes GS166719: MP:0010678 abnormal skin adnexa morphology
Expand Tier I Human 232 Genes GS176771: HP:0001000 Abnormality of skin pigmentation
Expand Tier I Mouse GO 2926 Genes GS183803: GO:0044267 cellular protein metabolic process
Expand Tier I Human CTD 4423 Genes GS123718: Ethinyl Estradiol interacting genes (MeSH:D004997) in CTD
Expand Tier I Mouse MP 220 Genes GS170240: MP:0001297 microphthalmia
Expand Tier I Mouse 514 Genes GS135247: adiposity 15 (Adip15, Published QTL Chr 10)
Expand Tier I Human CTD 1601 Genes GS123916: Aflatoxin B1 interacting genes (MeSH:D016604) in CTD
Expand Tier I Mouse 545 Genes GS136099: long bones 9 (Lbn9, Published QTL Chr 10)
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Mouse GO 4651 Genes GS177310: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Human 1228 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Mouse MP 3110 Genes GS167020: MP:0003956 abnormal body size
Expand Tier I Mouse GO 731 Genes GS193220: GO:0006082 organic acid metabolic process
Expand Tier I Mouse GO 148 Genes GS178392: GO:0016054 organic acid catabolic process
Expand Tier I Mouse 550 Genes GS135327: arthropathy in MRL and DBA/1 mice 1 (Artmd1, Published QTL Chr 10)
Expand Tier I Mouse GO 863 Genes GS177902: GO:0042802 identical protein binding
Expand Tier I Mouse GO 10 Genes GS189705: GO:0006570 tyrosine metabolic process
Expand Tier I Human GO 258 Genes GS197043: GO:0044282 small molecule catabolic process
Expand Tier I Human 49 Genes GS173815: HP:0000736 Short attention span
Expand Tier I Mouse MP 42 Genes GS167884: MP:0009358 environmentally induced seizures
Expand Tier I Human 30 Genes GS176897: HP:0002354 Memory impairment
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human GO 61 Genes GS208235: GO:0008652 cellular amino acid biosynthetic process
Expand Tier I Human 489 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human GO 2368 Genes GS207365: GO:0005829 cytosol
Expand Tier I Human 3 Genes GS172206: HP:0100324 Scleroderma
Expand Human 9 Genes GS221238: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PHENYLALANINE_METABOLISM
Expand Tier I Human GO 29 Genes GS206467: GO:0042558 pteridine-containing compound metabolic process
Expand Tier I Human GO 65 Genes GS208542: GO:0018958 phenol-containing compound metabolic process
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Mouse GO 143 Genes GS189214: GO:0004497 monooxygenase activity
Expand Tier I Human CTD 180 Genes GS122888: beta-Naphthoflavone interacting genes (MeSH:D019324) in CTD
Expand Tier I Human CTD 82 Genes GS123580: ciprofibrate interacting genes (MeSH:C019304) in CTD
Expand Tier I Mouse MP 403 Genes GS169080: MP:0002075 abnormal coat/hair pigmentation
Expand Tier I Mouse 558 Genes GS135635: collagen induced arthritis QTL 8 (Cia8, Published QTL Chr 10)
Expand Tier I Mouse MP 2199 Genes GS165244: MP:0010771 integument phenotype
Expand Tier I Human 941 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Mouse 545 Genes GS135699: directional asymmetry QTL 6 (Daq6, Published QTL Chr 10)
Expand Tier I Mouse MP 14488 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Mouse MP 661 Genes GS169386: MP:0002063 abnormal learning/memory/conditioning
Expand Tier I Human GO 260 Genes GS195145: GO:0016053 organic acid biosynthetic process
Expand Tier I Human 81 Genes GS174550: HP:0000958 Dry skin
Expand Tier I Human 498 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Mouse MP 663 Genes GS163398: MP:0005266 abnormal metabolism
Expand Tier I Mouse GO 13 Genes GS183024: GO:0009074 aromatic amino acid family catabolic process
Expand Tier I Human GO 4593 Genes GS204007: GO:0044700 single organism signaling
Expand Tier I Human GO 102 Genes GS197118: GO:0016597 amino acid binding
Expand Tier I Human GO 7336 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 113 Genes GS173647: HP:0012072 Aciduria
Expand Tier I Mouse 536 Genes GS135438: bone mineral density 38 (Bmd38, Published QTL Chr 10)
Expand Tier I Human 470 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier I Human 215 Genes GS176973: HP:0001072 Thickened skin
Expand Tier I Human 52 Genes GS177055: HP:0005599 Hypopigmentation of hair
Expand Tier I Mouse 515 Genes GS136941: vertebral trabecular bone trait 9 (Vtbt9, Published QTL Chr 10)
Expand Tier I Human CTD 5075 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Tier I Human CTD 291 Genes GS124722: kojic acid interacting genes (MeSH:C011890) in CTD
Expand Tier I Mouse 442 Genes GS135845: femoral cross-sectional area 3 (Fcsa3, Published QTL Chr 10)
Expand Tier I Human 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 409 Genes GS175670: HP:0007364 Aplasia/Hypoplasia of the cerebrum
Expand Tier I Mouse MP 98 Genes GS165787: MP:0001522 impaired swimming
Expand Tier I Mouse GO 8 Genes GS188766: GO:0046146 tetrahydrobiopterin metabolic process
Expand Tier I Mouse GO 487 Genes GS187771: GO:1901566 organonitrogen compound biosynthetic process
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human GO 162 Genes GS202464: GO:0016705 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
Expand Tier I Mouse 406 Genes GS136582: red blood cell QTL 4 (Rbcq4, Published QTL Chr 10)
Expand Tier I Mouse GO 148 Genes GS183585: GO:0046395 carboxylic acid catabolic process
Expand Tier I Mouse MP 951 Genes GS165427: MP:0000432 abnormal head morphology
Expand Tier I Human GO 735 Genes GS204608: GO:0019226 transmission of nerve impulse
Expand Tier I Human GO 260 Genes GS200383: GO:0046394 carboxylic acid biosynthetic process
Expand Tier I Human GO 846 Genes GS204326: GO:0019752 carboxylic acid metabolic process
Expand Tier I Human 273 Genes GS172516: HP:0001347 Hyperreflexia
Expand Tier I Human 545 Genes GS175015: HP:0001627 Abnormality of the heart
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 Mouse MP 1672 Genes GS165260: MP:0001392 abnormal locomotor behavior
Expand Tier I Human 65 Genes GS170884: HP:0006919 Abnormal aggressive, impulsive or violent behavior
Expand Tier I Mouse GO 6204 Genes GS184629: GO:0005515 protein binding
Expand Tier I Mouse MP 865 Genes GS167759: MP:0000787 abnormal telencephalon morphology
Expand Tier I Human 737 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Mouse GO 650 Genes GS187770: GO:1901565 organonitrogen compound catabolic process
Expand Human 169 Genes GS220916: http://www.broadinstitute.org/gsea/msigdb/cards/CARBOXYLIC_ACID_METABOLIC_PROCESS
Expand Tier I Human GO 2241 Genes GS209291: GO:0046914 transition metal ion binding
Expand Tier I Human 134 Genes GS175172: HP:0004354 Abnormality of carboxylic acid metabolism
Expand Tier I Mouse MP 1385 Genes GS163971: MP:0002092 abnormal eye morphology
Expand Tier I Human CTD 5725 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
Expand Tier I Human GO 858 Genes GS194645: GO:0042802 identical protein binding
Expand Tier I Mouse 493 Genes GS135614: circulating hormone level QTL 6 (Chlq6, Published QTL Chr 10)
Expand Tier I Human GO 1 Genes GS206583: GO:0006571 tyrosine biosynthetic process
Expand Tier I Human 203 Genes GS171621: HP:0100851 Abnormal emotion/affect behavior
Expand Tier I Human 21 Genes GS174052: HP:0000722 Obsessive-compulsive disorder
Expand Tier I Human CTD 1 Genes GS121745: peroxovanadate interacting genes (MeSH:C069276) in CTD
Expand Tier I Mouse 406 Genes GS136252: mean corpuscular volume QTL 3 (Mcvq3, Published QTL Chr 10)
Expand Tier I Human CTD 670 Genes GS121369: Clofibric Acid interacting genes (MeSH:D002995) in CTD
Expand Tier I Human 97 Genes GS173091: HP:0004374 Hemiplegia/hemiparesis
Expand Tier I Human GO 15 Genes GS199994: GO:0009713 catechol-containing compound biosynthetic process
Expand Tier I Mouse MP 2606 Genes GS165397: MP:0001265 decreased body size
Expand Tier I Mouse GO 1395 Genes GS185366: GO:0044248 cellular catabolic process
Expand Tier I Human GO 821 Genes GS194041: GO:1901361 organic cyclic compound catabolic process
Expand Tier I Human 12 Genes GS175233: HP:0002286 Fair hair
Expand Tier I Human GO 42 Genes GS196963: GO:0009712 catechol-containing compound metabolic process
Expand Tier I Mouse GO 1572 Genes GS192354: GO:0046914 transition metal ion binding
Expand Tier I Mouse MP 3543 Genes GS169095: MP:0004924 abnormal behavior
Expand Tier I Human GO 198 Genes GS200384: GO:0046395 carboxylic acid catabolic process
Expand Tier I Human GO 1236 Genes GS202899: GO:0050877 neurological system process
Expand Mouse 1153 Genes GS216490: Differential expression of the liver after chronic ethanol exposure in mice.
Expand Tier I Human 182 Genes GS173028: HP:0004360 Abnormality of acid-base homeostasis
Expand Tier I Mouse MP 238 Genes GS170688: MP:0002697 abnormal eye size
Expand Tier I Human GO 5 Genes GS196413: GO:0018126 protein hydroxylation
Expand Tier II Mouse 521 Genes GS84241: alcohol preference (Published QTL, Chr 10)
Expand Tier I Mouse MP 633 Genes GS163101: MP:0008540 abnormal cerebrum morphology
Expand Tier I Human GO 262 Genes GS202364: GO:0048037 cofactor binding
Expand Tier I Mouse 514 Genes GS136397: organ weight 6 (Org6, Published QTL Chr 10)
Expand Tier II Mouse 33 Genes GS36407: Whole Brain Gene expression correlates of Open Field - Total rears 5-10 minutes in Females & Males BXD
Expand Tier I Mouse GO 232 Genes GS177696: GO:0051186 cofactor metabolic process
Expand Tier I Human GO 6769 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Mouse 558 Genes GS136076: insulin QTL 9 (Insq9, Published QTL Chr 10)
Expand Tier I Human GO 5152 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Tier I Mouse GO 4286 Genes GS190949: GO:0009058 biosynthetic process
Expand Tier I Mouse MP 4592 Genes GS165537: MP:0005376 homeostasis/metabolism phenotype
Expand Tier I Mouse MP 1848 Genes GS167622: MP:0002152 abnormal brain morphology
Expand Tier I Human GO 1693 Genes GS209960: GO:0003008 system process
Expand Tier I Mouse MP 233 Genes GS166598: MP:0005332 abnormal amino acid level
Expand Tier I Mouse GO 3005 Genes GS177308: GO:1901362 organic cyclic compound biosynthetic process
Expand Tier I Human CTD 3171 Genes GS127127: Benzo(a)pyrene interacting genes (MeSH:D001564) in CTD
Expand Tier I Mouse MP 1007 Genes GS164742: MP:0001732 postnatal growth retardation
Expand Tier I Human 57 Genes GS174179: HP:0002514 Cerebral calcification
Expand Tier I Human GO 93 Genes GS206081: GO:0004497 monooxygenase activity
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 Mouse 539 Genes GS135326: age related thymic involution 2 (Arti2, Published QTL Chr 10)
Expand Tier I Human 24 Genes GS174509: HP:0100716 Autoagression
Expand Tier I Mouse MP 932 Genes GS166585: MP:0001510 abnormal coat appearance
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Mouse MP 119 Genes GS165472: MP:0003638 abnormal response/metabolism to endogenous compounds
Expand Tier I Mouse MP 129 Genes GS168632: MP:0000371 diluted coat color
Expand Tier I Human GO 2464 Genes GS199032: GO:0036211 protein modification process
Expand Tier I Mouse 539 Genes GS135585: cholesterol absorption 2 (Chab2, Published QTL Chr 10)
Expand Tier I Mouse GO 196 Genes GS180264: GO:0044282 small molecule catabolic process
Expand Tier I Human 167 Genes GS171201: HP:0001941 Acidosis
Expand Tier I Mouse 532 Genes GS136072: insulin QTL 4 (Insq4, Published QTL Chr 10)
Expand Tier I Human 258 Genes GS172272: HP:0001197 Abnormality of prenatal development or birth
Expand Tier I Human GO 2558 Genes GS194336: GO:0043412 macromolecule modification
Expand Tier I Mouse GO 9049 Genes GS180166: GO:0008152 metabolic process
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Human 132 Genes GS219791: http://www.broadinstitute.org/gsea/msigdb/cards/AMINE_METABOLIC_PROCESS
Expand Tier I Human GO 7 Genes GS205626: GO:0046146 tetrahydrobiopterin metabolic process
Expand Tier I Human GO 645 Genes GS204631: GO:1901566 organonitrogen compound biosynthetic process
Expand Tier I Mouse MP 1013 Genes GS164724: MP:0001516 abnormal motor coordination/ balance
Expand Tier I Mouse 551 Genes GS136151: "lupus in MRL and B6 F2 cross, QTL 4" (Lmb4, Published QTL Chr 10)
Expand Tier II Mouse 101 Genes GS36362: Whole Brain Gene expression correlates of Open Field - Total rears 0-5 minutes in Females & Males BXD
Expand Tier I Mouse MP 1476 Genes GS169531: MP:0005391 vision/eye phenotype
Expand Tier I Human 391 Genes GS175537: HP:0011277 Abnormality of the urinary system physiology
Expand Tier I Human 472 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Mouse GO 68 Genes GS187274: GO:0009063 cellular amino acid catabolic process
Expand Tier I Human 95 Genes GS176560: HP:0001010 Hypopigmentation of the skin
Expand Tier I Mouse GO 580 Genes GS177903: GO:0042803 protein homodimerization activity
Expand Tier I Mouse GO 7 Genes GS180048: GO:0016714 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced pteridine as one donor, and incorporation of one atom of oxygen
Expand Tier I Mouse MP 1825 Genes GS168956: MP:0003491 abnormal voluntary movement
Expand Tier II Mouse 73 Genes GS36367: Whole Brain Gene expression correlates of Open Field - Total rears 0-5 minutes in Females BXD
Expand Tier I Human GO 15 Genes GS206167: GO:0046189 phenol-containing compound biosynthetic process
Expand Tier I Mouse 537 Genes GS136675: skull morphology 14 (Skull14, Published QTL Chr 10)
Expand Tier I Mouse 535 Genes GS136235: mandible length 9 (Manln9, Published QTL Chr 10)
Expand Tier I Human GO 137 Genes GS201740: GO:0001505 regulation of neurotransmitter levels
Expand Tier I Mouse 493 Genes GS135606: circulating hormone level QTL 15 (Chlq15, Published QTL Chr 10)
Expand Tier I Human 616 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse MP 3924 Genes GS163934: MP:0001764 abnormal homeostasis
Expand Tier I Human 144 Genes GS175128: HP:0011123 Inflammatory abnormality of the skin
Expand Tier I Human GO 6651 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human GO 1 Genes GS199832: GO:0009073 aromatic amino acid family biosynthetic process
Expand Tier I Human 543 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human 5 Genes GS172502: HP:0004923 Hyperphenylalaninemia
Expand Human 69 Genes GS220918: http://www.broadinstitute.org/gsea/msigdb/cards/AMINO_ACID_METABOLIC_PROCESS
Expand Mouse 1153 Genes GS216461: Differential expression of the liver after chronic ethanol exposure in mice.
Expand Tier I Mouse GO 1 Genes GS192782: GO:0009095 aromatic amino acid family biosynthetic process, prephenate pathway
Expand Tier I Human GO 5379 Genes GS203642: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Mouse GO 165 Genes GS185632: GO:0016705 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
Expand Tier I Mouse MP 1688 Genes GS168174: MP:0001919 abnormal reproductive system physiology
Expand Tier I Mouse MP 111 Genes GS170039: MP:0011496 abnormal head size
Expand Tier I Human GO 5601 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human 346 Genes GS171309: HP:0000252 Microcephaly
Expand Tier I Human GO 5558 Genes GS194040: GO:1901360 organic cyclic compound metabolic process