Gene Details



DLAT and homologs in 1 species are found in 199 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 Human 4 Genes GS172116: HP:0002457 Abnormal head movements
Expand Tier I Human GO 77 Genes GS208956: GO:0006007 glucose catabolic process
Expand Tier I Human GO 741 Genes GS201250: GO:0044429 mitochondrial part
Expand Tier I Human GO 52 Genes GS210158: GO:0006084 acetyl-CoA metabolic process
Expand Tier I Human GO 63 Genes GS197596: GO:0006096 glycolysis
Expand Tier I Human GO 333 Genes GS204027: GO:0044708 single-organism behavior
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
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 173 Genes GS128223: Proteins found to be modified by at least two drugs of abuse
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
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 Tier I Human GO 6 Genes GS197577: GO:0016417 S-acyltransferase activity
Expand Tier I Human 1228 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human GO 1597 Genes GS207991: GO:0000003 reproduction
Expand Tier I Human GO 250 Genes GS201922: GO:0019318 hexose metabolic process
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human GO 3324 Genes GS210180: GO:0031326 regulation of cellular biosynthetic process
Expand Tier I Human GO 14 Genes GS206920: GO:0051196 regulation of coenzyme metabolic process
Expand Tier I Human GO 15 Genes GS210159: GO:0006085 acetyl-CoA biosynthetic process
Expand Tier I Human GO 590 Genes GS205780: GO:0044723 single-organism carbohydrate metabolic process
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 GO 450 Genes GS197593: GO:0006091 generation of precursor metabolites and energy
Expand Human 49 Genes GS222196: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_ARACHIDONIC_ACID_METABOLISM
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 8137 Genes GS202316: GO:0050789 regulation of biological process
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human GO 3354 Genes GS205622: GO:0009889 regulation of biosynthetic process
Expand Tier I Human GO 1592 Genes GS196196: GO:0022414 reproductive process
Expand Tier I Human 50 Genes GS173113: HP:0002186 Apraxia
Expand Tier I Human GO 93 Genes GS193942: GO:0035383 thioester metabolic process
Expand Tier I Human GO 3861 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 70 Genes GS209130: GO:0044704 single-organism reproductive behavior
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 Tier III Human 3178 Genes GS137407: Supplementary Table 2. Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human 344 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Human 255 Genes GS176610: HP:0003593 Infantile onset
Expand Tier I Human GO 12 Genes GS210160: GO:0006086 acetyl-CoA biosynthetic process from pyruvate
Expand Tier I Human GO 30 Genes GS197721: GO:0030431 sleep
Expand Tier I Human GO 810 Genes GS195897: GO:0044255 cellular lipid metabolic process
Expand Human 62 Genes GS219849: http://www.broadinstitute.org/gsea/msigdb/cards/EPIDERMIS_DEVELOPMENT
Expand Tier I Human 167 Genes GS171201: HP:0001941 Acidosis
Expand Tier I Human 14 Genes GS172228: HP:0002194 Delayed gross motor development
Expand Tier I Human 89 Genes GS176345: HP:0003128 Lactic acidosis
Expand Tier III Human 735 Genes GS1229: Differential gene expression among Heroin Abusers
Expand Tier I Human GO 403 Genes GS199550: GO:0032787 monocarboxylic acid metabolic process
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human GO 1 Genes GS207967: GO:0030523 dihydrolipoamide S-acyltransferase activity
Expand Tier I Human GO 507 Genes GS206091: GO:0007610 behavior
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human 472 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Human GO 202 Genes GS194778: GO:0042180 cellular ketone metabolic process
Expand Tier I Human 491 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Human GO 2 Genes GS197584: GO:0016418 S-acetyltransferase activity
Expand Tier I Human GO 2719 Genes GS199273: GO:0043233 organelle lumen
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 14 Genes GS206922: GO:0051193 regulation of cofactor metabolic process
Expand Tier I Human CTD 78 Genes GS126445: Dehydroepiandrosterone interacting genes (MeSH:D003687) in CTD
Expand Tier I Human 135 Genes GS172857: HP:0004305 Involuntary movements
Expand Tier I Human 45 Genes GS176166: HP:0001256 Intellectual disability, mild
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human CTD 527 Genes GS125792: Ethanol interacting genes (MeSH:D000431) in CTD
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human CTD 287 Genes GS123026: Haloperidol interacting genes (MeSH:D006220) in CTD
Expand Tier I Human 786 Genes GS176107: HP:0000929 Abnormality of the skull
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 280 Genes GS207949: GO:0005996 monosaccharide metabolic process
Expand Tier I Human 222 Genes GS173995: HP:0000508 Ptosis
Expand Tier I Human 31 Genes GS175341: HP:0100755 Abnormality of salivation
Expand Tier I Human 498 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 699 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human 472 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human GO 5223 Genes GS207857: GO:0009058 biosynthetic process
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 92 Genes GS197534: GO:0019320 hexose catabolic process
Expand Tier I Human GO 1138 Genes GS193812: GO:0006629 lipid metabolic process
Expand Tier I Human GO 4377 Genes GS210182: GO:0031323 regulation of cellular metabolic process
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 Human 4 Genes GS171945: HP:0002268 Paroxysmal dystonia
Expand Tier I Human GO 5 Genes GS201363: GO:0045254 pyruvate dehydrogenase complex
Expand Tier I Human GO 7336 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human GO 137 Genes GS205788: GO:0044724 single-organism carbohydrate catabolic process
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 106 Genes GS173246: HP:0001332 Dystonia
Expand Tier I Human 470 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier I Human GO 97 Genes GS197709: GO:0046365 monosaccharide catabolic process
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human GO 214 Genes GS208955: GO:0006006 glucose metabolic process
Expand Tier I Human GO 168 Genes GS195597: GO:0010565 regulation of cellular ketone metabolic process
Expand Human 62 Genes GS221415: http://www.broadinstitute.org/gsea/msigdb/cards/EPIDERMIS_DEVELOPMENT
Expand Tier I Human GO 133 Genes GS194442: GO:0051188 cofactor biosynthetic process
Expand Tier I Human 20 Genes GS176236: HP:0002307 Drooling
Expand Tier I Human 416 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human CTD 738 Genes GS126989: Hydralazine interacting genes (MeSH:D006830) in CTD
Expand Tier I Human CTD 5075 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Tier I Human GO 31 Genes GS197594: GO:0006090 pyruvate metabolic process
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 143 Genes GS176586: HP:0001270 Motor delay
Expand Tier I Human 543 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human GO 13 Genes GS194104: GO:0050812 regulation of acyl-CoA biosynthetic process
Expand Tier I Human 534 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier I Human GO 218 Genes GS200311: GO:0019216 regulation of lipid metabolic process
Expand Tier I Human 409 Genes GS175670: HP:0007364 Aplasia/Hypoplasia of the cerebrum
Expand Tier I Human 316 Genes GS170825: HP:0002167 Neurological speech impairment
Expand Tier I Human GO 4314 Genes GS204746: GO:0080090 regulation of primary metabolic process
Expand Tier I Human GO 3275 Genes GS199267: GO:0043234 protein complex
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 Tier I Human CTD 2047 Genes GS127205: Tamoxifen interacting genes (MeSH:D013629) in CTD
Expand Tier I Human GO 1216 Genes GS199495: GO:0051174 regulation of phosphorus metabolic process
Expand Tier I Human 261 Genes GS176172: HP:0001251 Ataxia
Expand Tier I Human GO 4811 Genes GS204612: GO:0019222 regulation of metabolic process
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
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 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 416 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human CTD 334 Genes GS122653: Clozapine interacting genes (MeSH:D003024) in CTD
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 Tier I Human GO 2494 Genes GS209235: GO:0006793 phosphorus metabolic process
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 175 Genes GS208737: GO:0016747 transferase activity, transferring acyl groups other than amino-acyl groups
Expand Tier I Human 35 Genes GS176798: HP:0001266 Choreoathetosis
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 CTD 323 Genes GS121837: bexarotene interacting genes (MeSH:C095105) in CTD
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 5047 Genes GS210357: GO:0044249 cellular biosynthetic process
Expand Tier I Human GO 953 Genes GS202555: GO:0043436 oxoacid metabolic process
Expand Human 62 Genes GS221166: http://www.broadinstitute.org/gsea/msigdb/cards/EPIDERMIS_DEVELOPMENT
Expand Tier I Human GO 6585 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human GO 1 Genes GS194890: GO:0004742 dihydrolipoyllysine-residue acetyltransferase activity
Expand Tier I Human 33 Genes GS172620: HP:0000657 Oculomotor apraxia
Expand Tier I Human GO 230 Genes GS208736: GO:0016746 transferase activity, transferring acyl groups
Expand Tier I Human GO 140 Genes GS195144: GO:0016052 carbohydrate catabolic process
Expand Tier I Human CTD 5725 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
Expand Tier I Human 416 Genes GS173146: HP:0011282 Abnormality of the hindbrain
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 GO 1 Genes GS195465: GO:0005967 mitochondrial pyruvate dehydrogenase complex
Expand Tier I Human GO 8702 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human GO 278 Genes GS194621: GO:0005759 mitochondrial matrix
Expand Tier I Human GO 84 Genes GS202961: GO:0019098 reproductive behavior
Expand Tier I Human GO 91 Genes GS201970: GO:0016407 acetyltransferase activity
Expand Tier I Human GO 257 Genes GS194434: GO:0051186 cofactor metabolic process
Expand Tier I Human 398 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 12 Genes GS208576: GO:0010510 regulation of acetyl-CoA biosynthetic process from pyruvate
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human GO 105 Genes GS202497: GO:0009108 coenzyme biosynthetic process
Expand Tier I Human 53 Genes GS175407: HP:0002072 Chorea
Expand Tier I Human GO 790 Genes GS199922: GO:0005975 carbohydrate metabolic process
Expand Tier I Human GO 971 Genes GS210163: GO:0006082 organic acid metabolic process
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 7689 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier I Human GO 1165 Genes GS206696: GO:0044702 single organism reproductive process
Expand Tier I Human GO 5321 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human GO 36 Genes GS194979: GO:0071616 acyl-CoA biosynthetic process
Expand Tier I Human GO 36 Genes GS193945: GO:0035384 thioester biosynthetic process
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 1 Genes GS176072: HP:0006961 Jerky head movements
Expand Tier I Human 5 Genes GS172653: HP:0002465 Poor speech
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 1736 Genes GS208734: GO:0016740 transferase activity
Expand Tier I Human 53 Genes GS173697: HP:0001319 Neonatal hypotonia
Expand Tier I Human GO 82 Genes GS200310: GO:0019217 regulation of fatty acid 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 Human GO 5152 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Tier I Human DRG 911 Genes provisional GS86977: Table S1: All transcripts significantly different in abundance between the majority of heroin subjects and their matched controls [DRG]
Expand Tier I Human GO 93 Genes GS198220: GO:0006637 acyl-CoA metabolic process
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 21 Genes GS176207: HP:0003781 Excessive salivation
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle