Gene Details



HSD17B10 and homologs in 6 species are found in 356 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 GO 1684 Genes GS204629: GO:1901564 organonitrogen compound metabolic process
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 99 Genes GS175130: HP:0000750 Delayed speech and language development
Expand Tier I Human CTD 1392 Genes GS126475: tert-Butylhydroperoxide interacting genes (MeSH:D020122) in CTD
Expand Tier I Mouse GO 919 Genes GS178388: GO:0055114 oxidation-reduction process
Expand Tier I Human GO 200 Genes GS200597: GO:0008406 gonad development
Expand Tier I Mouse GO 361 Genes GS179795: GO:0019866 organelle inner membrane
Expand Tier I Human 491 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Human GO 2719 Genes GS199273: GO:0043233 organelle lumen
Expand Tier I Human 44 Genes GS174662: HP:0001423 X-linked dominant inheritance
Expand Tier I Human GO 713 Genes GS204630: GO:1901565 organonitrogen compound catabolic process
Expand Tier I Human GO 2625 Genes GS196343: GO:0036094 small molecule binding
Expand Tier I Mouse GO 8406 Genes GS177404: GO:0005737 cytoplasm
Expand Tier I Mouse GO 1 Genes GS180734: GO:0018454 acetoacetyl-CoA reductase activity
Expand Tier I Human GO 339 Genes GS195494: GO:0006520 cellular amino acid metabolic process
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Mouse GO 88 Genes GS189527: GO:0051262 protein tetramerization
Expand Tier I Mouse GO 3615 Genes GS178359: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human GO 3917 Genes GS203908: GO:0016070 RNA metabolic process
Expand Tier I Mouse GO 58 Genes GS190874: GO:0035258 steroid hormone receptor binding
Expand Tier I Human CTD 709 Genes GS126466: Quercetin interacting genes (MeSH:D011794) in CTD
Expand Tier I Human 1 Genes GS171632: HP:0009062 Infantile axial hypotonia
Expand Tier I Human GO 8 Genes GS208895: GO:0003857 3-hydroxyacyl-CoA dehydrogenase activity
Expand Tier I Human CTD 92 Genes GS125392: 4-tert-octylphenol interacting genes (MeSH:C105260) in CTD
Expand Tier I Human GO 4371 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Human GO 2432 Genes GS209108: GO:0000166 nucleotide binding
Expand Tier I Human GO 953 Genes GS202555: GO:0043436 oxoacid metabolic process
Expand Tier I Human GO 153 Genes GS205102: GO:0051427 hormone receptor binding
Expand Tier I Human 50 Genes GS173812: HP:0000738 Hallucinations
Expand Tier I Mouse GO 650 Genes GS191728: GO:0008289 lipid binding
Expand Tier I Human GO 85 Genes GS206397: GO:0051262 protein tetramerization
Expand Tier I Mouse GO 31 Genes GS186326: GO:0016229 steroid dehydrogenase activity
Expand Tier I Human 260 Genes GS170933: HP:0001288 Gait disturbance
Expand Tier I Mouse GO 1209 Genes GS178284: GO:0031090 organelle membrane
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human 35 Genes GS172453: HP:0008936 Muscular hypotonia of the trunk
Expand Tier I Mouse 3319 Genes GS127931: Olfactory bulb - Allen Mouse Brain Atlas
Expand Tier I Human GO 105 Genes GS204132: GO:0009063 cellular amino acid catabolic process
Expand Tier I Mouse GO 1172 Genes GS178426: GO:0005102 receptor binding
Expand Tier I Human 319 Genes GS176591: HP:0001276 Hypertonia
Expand Tier I Human 10 Genes GS174306: HP:0000713 Agitation
Expand Tier I Human 47 Genes GS175737: HP:0001238 Slender finger
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 384 Genes GS171708: HP:0000359 Abnormality of the inner ear
Expand Tier I Mouse GO 714 Genes GS182173: GO:0031967 organelle envelope
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Human GO 11 Genes GS203050: GO:0004303 estradiol 17-beta-dehydrogenase activity
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier III Mouse 6105 Genes GS213074: Genes with suggestive difference in (B6PF1) vs (PB6F1 + B6 + PWD) comparison
Expand Tier III Mouse 8003 Genes GS213041: Expression profiles of aging in C57BL/6 mouse hippocampal tissue
Expand Tier I Human 105 Genes GS171199: HP:0001943 Hypoglycemia
Expand Tier I Human 60 Genes GS174300: HP:0000718 Aggressive behavior
Expand Tier I Mouse 2963 Genes GS127934: Retrohippocampal region - Allen Mouse Brain Atlas
Expand Tier I Human GO 5452 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Human GO 4097 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human GO 102 Genes GS195263: GO:0008584 male gonad development
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 CTD 238 Genes GS121381: fumonisin B1 interacting genes (MeSH:C056933) in CTD
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 GO 5103 Genes GS192512: GO:0003824 catalytic activity
Expand Tier I Human GO 7808 Genes GS207616: GO:0016020 membrane
Expand Tier I Human GO 655 Genes GS197734: GO:0006396 RNA processing
Expand Tier I Human 784 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human GO 198 Genes GS195142: GO:0016054 organic acid catabolic process
Expand Tier I Human GO 505 Genes GS198971: GO:0031966 mitochondrial membrane
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 351 Genes GS198058: GO:0005743 mitochondrial inner membrane
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 271 Genes GS202998: GO:0061458 reproductive system development
Expand Tier I Human GO 1518 Genes GS194138: GO:0005739 mitochondrion
Expand Tier I Human 35 Genes GS176798: HP:0001266 Choreoathetosis
Expand Tier I Human GO 204 Genes GS210307: GO:0034470 ncRNA processing
Expand Tier I Mouse 3267 Genes GS127938: Striatum - Allen Mouse Brain Atlas
Expand Tier II Mouse 41 Genes GS35394: Whole Brain Gene expression correlates of Mechanical Sensitivity-Von Frey Threshold in Males BXD
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Human GO 1993 Genes GS207862: GO:0009056 catabolic process
Expand Tier I Mouse 310 Genes GS136739: small testis weight 2 (Smtw2, Published QTL Chr X)
Expand Tier I Human GO 2545 Genes GS203335: GO:0048513 organ development
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Human GO 73 Genes GS204316: GO:0007569 cell aging
Expand Tier I Mouse 299 Genes GS136144: lithogenic gene 4 (Lith4, Published QTL Chr X)
Expand Tier I Human 46 Genes GS175267: HP:0001166 Arachnodactyly
Expand Tier I Mouse GO 229 Genes GS189525: GO:0051260 protein homooligomerization
Expand Tier I Human GO 230 Genes GS209107: GO:0045137 development of primary sexual characteristics
Expand Tier I Human GO 2373 Genes GS195036: GO:0031090 organelle membrane
Expand Tier I Human 160 Genes GS175806: HP:0001417 X-linked inheritance
Expand Tier I Human GO 278 Genes GS194621: GO:0005759 mitochondrial matrix
Expand Tier I Human GO 774 Genes GS208730: GO:0070271 protein complex biogenesis
Expand Tier I Human 108 Genes GS176797: HP:0001268 Mental deterioration
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 116 Genes GS198446: GO:0016616 oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 53 Genes GS175407: HP:0002072 Chorea
Expand Tier I Human GO 5369 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier I Human 388 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Human GO 259 Genes GS202414: GO:0044712 single-organism catabolic process
Expand Tier I Mouse GO 67 Genes GS187387: GO:0005496 steroid binding
Expand Tier I Human GO 741 Genes GS201250: GO:0044429 mitochondrial part
Expand Tier I Human GO 66 Genes GS207778: GO:0035258 steroid hormone receptor binding
Expand Tier I Mouse GO 26 Genes GS189007: GO:0033764 steroid dehydrogenase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
Expand Tier I Mouse GO 2439 Genes GS179580: GO:0036094 small molecule binding
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
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 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 1228 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human GO 1544 Genes GS195733: GO:0022607 cellular component assembly
Expand Tier I Mouse GO 863 Genes GS177902: GO:0042802 identical protein binding
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Human 215 Genes GS176167: HP:0001257 Spasticity
Expand Tier I Human 553 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human GO 337 Genes GS202075: GO:0051259 protein oligomerization
Expand Tier I Human GO 258 Genes GS197043: GO:0044282 small molecule catabolic process
Expand Tier I Human GO 135 Genes GS207783: GO:0035257 nuclear hormone receptor binding
Expand Tier I Mouse 288 Genes GS136623: Stem cell proliferation 11 (Scpro11, Published QTL Chr X)
Expand Tier I Mouse 3096 Genes GS127928: Lateral septal complex - Allen Mouse Brain Atlas
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 I Mouse 2918 Genes GS127935: Striatum dorsal region - Allen Mouse Brain Atlas
Expand Tier I Mouse GO 50 Genes GS182722: GO:0051287 NAD binding
Expand Tier I Human GO 25 Genes GS205871: GO:0033764 steroid dehydrogenase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier III Mouse 8107 Genes GS213076: Genes with suggestive difference in (B6) vs (B6PF1 + PB6F1 + PWD) comparison
Expand Tier I Mouse GO 98 Genes GS190879: GO:0035257 nuclear hormone receptor binding
Expand Tier I Mouse GO 180 Genes GS185926: GO:0050662 coenzyme binding
Expand Tier I Human GO 260 Genes GS195560: GO:0007548 sex differentiation
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 Human GO 893 Genes GS203289: GO:0071822 protein complex subunit organization
Expand Tier I Human GO 819 Genes GS198970: GO:0031967 organelle envelope
Expand Tier I Human GO 4283 Genes GS197009: GO:0005886 plasma membrane
Expand Tier I Human 498 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human GO 7336 Genes GS201431: GO:0005515 protein binding
Expand Tier I Mouse GO 727 Genes GS179828: GO:0006461 protein complex assembly
Expand Tier I Human GO 29 Genes GS203172: GO:0016229 steroid dehydrogenase activity
Expand Tier I Human GO 2824 Genes GS209411: GO:0048869 cellular developmental process
Expand Tier I Human CTD 5075 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Tier I Human 287 Genes GS175594: HP:0011014 Abnormal glucose homeostasis
Expand Tier I Human GO 173 Genes GS206159: GO:0033218 amide binding
Expand Tier I Human 316 Genes GS170825: HP:0002167 Neurological speech impairment
Expand Tier I Human 35 Genes GS173309: HP:0002938 Lumbar hyperlordosis
Expand Tier I Mouse GO 4224 Genes GS193059: GO:0044446 intracellular organelle part
Expand Tier II Mouse 150 Genes GS35294: Whole Brain Gene expression correlates of Prepulse inhibition at 85db in Females BXD
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 50 Genes GS175148: HP:0010511 Long toe
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Mouse GO 58 Genes GS182720: GO:0051289 protein homotetramerization
Expand Tier I Human 529 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human GO 846 Genes GS204326: GO:0019752 carboxylic acid metabolic process
Expand Tier II Mouse 150 Genes GS35314: Whole Brain Gene expression correlates of Acoustic Startle Response Percentage of maximum response at 85 db in Females BXD
Expand Tier I Human 273 Genes GS172516: HP:0001347 Hyperreflexia
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 65 Genes GS170884: HP:0006919 Abnormal aggressive, impulsive or violent behavior
Expand Tier I Human 10 Genes GS171329: HP:0008947 Infantile muscular hypotonia
Expand Tier I Mouse GO 6204 Genes GS184629: GO:0005515 protein binding
Expand Tier I Human GO 738 Genes GS208665: GO:0008289 lipid binding
Expand Tier I Human GO 119 Genes GS195315: GO:0046546 development of primary male sexual characteristics
Expand Tier I Human 33 Genes GS174504: HP:0000709 Psychosis
Expand Tier I Human GO 78 Genes GS204583: GO:0008033 tRNA processing
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 Human GO 543 Genes GS200514: GO:0048610 cellular process involved in reproduction
Expand Tier I Human 203 Genes GS171621: HP:0100851 Abnormal emotion/affect behavior
Expand Tier I Human 78 Genes GS172684: HP:0003307 Hyperlordosis
Expand Tier I Mouse GO 949 Genes GS189780: GO:0043933 macromolecular complex subunit organization
Expand Tier I Human GO 198 Genes GS200384: GO:0046395 carboxylic acid catabolic process
Expand Tier I Human 578 Genes GS172030: HP:0000365 Hearing impairment
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 Human GO 4567 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human GO 262 Genes GS202364: GO:0048037 cofactor binding
Expand Tier I Mouse 3375 Genes GS127927: Hypothalamus - Allen Mouse Brain Atlas
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 4713 Genes GS205364: GO:0010467 gene expression
Expand Tier I Human GO 271 Genes GS196165: GO:0048608 reproductive structure development
Expand Tier I Human GO 126 Genes GS197729: GO:0006399 tRNA metabolic process
Expand Tier I Human GO 772 Genes GS196593: GO:0006461 protein complex assembly
Expand Tier I Human GO 6769 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human GO 1 Genes GS197531: GO:0018454 acetoacetyl-CoA reductase activity
Expand Tier I Human GO 186 Genes GS202764: GO:0050662 coenzyme binding
Expand Tier I Mouse 288 Genes GS135733: dietary obesity 7 (Dob7, Published QTL Chr X)
Expand Tier I Mouse GO 2263 Genes GS192174: GO:0000166 nucleotide binding
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human GO 1597 Genes GS207991: GO:0000003 reproduction
Expand Tier I Human GO 6278 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Mouse 3289 Genes GS127924: Cerebral cortex - Allen Mouse Brain Atlas
Expand Tier I Mouse 3384 Genes GS127925: Hippocampal formation - Allen Mouse Brain Atlas
Expand Tier I Mouse 223 Genes GS135779: exercise endurance QTL 1 (Eeq1, Published QTL Chr X)
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 599 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Human GO 55 Genes GS199519: GO:0051289 protein homotetramerization
Expand Tier I Human GO 1592 Genes GS196196: GO:0022414 reproductive process
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Mouse GO 868 Genes GS180149: GO:0065003 macromolecular complex assembly
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 289 Genes GS199289: GO:0034660 ncRNA metabolic process
Expand Tier I Mouse GO 120 Genes GS188247: GO:0051427 hormone receptor binding
Expand Tier I Mouse GO 4588 Genes GS177309: GO:1901363 heterocyclic compound binding
Expand Tier I Human 398 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Human 255 Genes GS176610: HP:0003593 Infantile onset
Expand Tier I Human GO 1 Genes GS199031: GO:0008709 cholate 7-alpha-dehydrogenase activity
Expand Tier I Human GO 48 Genes GS199521: GO:0051287 NAD binding
Expand Tier I Human 167 Genes GS171201: HP:0001941 Acidosis
Expand Tier I Mouse GO 342 Genes GS181270: GO:0005743 mitochondrial inner membrane
Expand Tier I Human 89 Genes GS176345: HP:0003128 Lactic acidosis
Expand Tier I Human GO 27 Genes GS204046: GO:0001540 beta-amyloid binding
Expand Tier I Human 263 Genes GS176145: HP:0001780 Abnormality of toe
Expand Tier I Mouse GO 9049 Genes GS180166: GO:0008152 metabolic process
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 2433 Genes GS203886: GO:1901265 nucleoside phosphate binding
Expand Tier I Human GO 4446 Genes GS203072: GO:0090304 nucleic acid metabolic process
Expand Tier I Human GO 424 Genes GS209955: GO:0003006 developmental process involved in reproduction
Expand Tier I Mouse GO 1149 Genes GS179957: GO:0005783 endoplasmic reticulum
Expand Tier I Mouse GO 4637 Genes GS177382: GO:0097159 organic cyclic compound binding
Expand Tier I Mouse 2944 Genes GS127937: Striatum-like amygdalar nuclei - Allen Mouse Brain Atlas
Expand Tier I Human GO 226 Genes GS206395: GO:0051260 protein homooligomerization
Expand Tier I Human GO 73 Genes GS204249: GO:0005496 steroid binding
Expand Tier I Human 426 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Mouse 2962 Genes GS127936: Striatum ventral region - Allen Mouse Brain Atlas
Expand Tier I Human 19 Genes GS171042: HP:0002344 Progressive neurologic deterioration
Expand Tier I Human 472 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human 50 Genes GS171198: HP:0001942 Metabolic acidosis
Expand Tier I Human GO 1685 Genes GS199112: GO:0044085 cellular component biogenesis
Expand Tier I Human GO 2673 Genes GS205543: GO:0070013 intracellular organelle lumen
Expand Tier I Human 51 Genes GS174123: HP:0100807 Long fingers
Expand Tier I Human GO 1138 Genes GS193812: GO:0006629 lipid metabolic process
Expand Tier I Mouse GO 182 Genes GS182661: GO:0042277 peptide binding
Expand Tier I Mouse GO 8145 Genes GS190714: GO:0016020 membrane
Expand Tier I Mouse GO 138 Genes GS181655: GO:0016614 oxidoreductase activity, acting on CH-OH group of donors
Expand Tier I Human 780 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
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 GO 4333 Genes GS184452: GO:0044422 organelle part
Expand Tier I Human GO 4213 Genes GS195112: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human GO 6651 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 143 Genes GS176586: HP:0001270 Motor delay
Expand Tier I Human 543 Genes GS175673: HP:0100022 Abnormality of movement
Expand Mouse 1153 Genes GS216461: Differential expression of the liver after chronic ethanol exposure in mice.
Expand Human 1417 Genes GS219730: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Tier I Human GO 1160 Genes GS206657: GO:0043933 macromolecular complex subunit organization
Expand Tier I Human GO 5379 Genes GS203642: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Human 381 Genes GS175714: HP:0011389 Functional abnormality of the inner ear
Expand Tier I Human GO 5601 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Mouse GO 2263 Genes GS187023: GO:1901265 nucleoside phosphate binding
Expand Tier I Human GO 163 Genes GS199456: GO:0042277 peptide binding
Expand Tier I Mouse GO 189 Genes GS189291: GO:0033218 amide binding
Expand Tier I Human GO 13 Genes GS201824: GO:0033327 Leydig cell differentiation
Expand Tier III Mouse 470 Genes GS216882: Co-expression cluster of haloperidol-induced catalepsy genes in striatum of HS mice short term selected lines. Dark Grey Cluster
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 5558 Genes GS194040: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Human GO 128 Genes GS198444: GO:0016614 oxidoreductase activity, acting on CH-OH group of donors
Expand Tier I Rat DRG 4920 Genes GS86932: Table S3: CORTEX 17K MICROARRAY [DRG]
Expand Tier I Human 368 Genes GS170971: HP:0000407 Sensorineural hearing impairment
Expand Tier I Human CTD 746 Genes GS125403: Diethylstilbestrol interacting genes (MeSH:D004054) in CTD
Expand Tier I Human GO 7311 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human 320 Genes GS175597: HP:0011013 Abnormality of carbohydrate metabolism/homeostasis
Expand Tier I Human 515 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Mouse GO 482 Genes GS181271: GO:0005740 mitochondrial envelope
Expand Tier I Human CTD 766 Genes GS124457: Mustard Gas interacting genes (MeSH:D009151) in CTD
Expand Tier I Human GO 127 Genes GS206630: GO:0046661 male sex differentiation
Expand Tier I Human CTD 4389 Genes GS123768: Cyclosporine interacting genes (MeSH:D016572) in CTD
Expand Tier I Mouse GO 1334 Genes GS178975: GO:0022607 cellular component assembly
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Human 82 Genes GS175765: HP:0001419 X-linked recessive inheritance
Expand Tier I Human GO 8702 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human CTD 22 Genes GS125385: prochloraz interacting genes (MeSH:C045362) in CTD
Expand Tier I Human GO 1211 Genes GS195176: GO:0005102 receptor binding
Expand Tier I Mouse GO 30 Genes GS180381: GO:0030331 estrogen receptor binding
Expand Tier I Human GO 971 Genes GS210163: GO:0006082 organic acid metabolic process
Expand Tier I Human GO 5321 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Human GO 381 Genes GS196559: GO:0019866 organelle inner membrane
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human GO 5216 Genes GS208954: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Human 832 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 537 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Tier I Mouse GO 5588 Genes GS193061: GO:0044444 cytoplasmic part
Expand Tier I Mouse GO 8630 Genes GS192624: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse GO 8650 Genes GS186743: GO:0043227 membrane-bounded organelle
Expand Tier I Human 166 Genes GS171901: HP:0010985 Gonosomal inheritance
Expand Tier I Human GO 19 Genes GS197214: GO:0009083 branched-chain amino acid catabolic process
Expand Tier I Human 17 Genes GS172163: HP:0000711 Restlessness
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 Mouse GO 728 Genes GS191792: GO:0070271 protein complex biogenesis
Expand Tier I Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Human GO 5400 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Human GO 2661 Genes GS207797: GO:0030154 cell differentiation
Expand Tier I Human GO 4070 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Mouse GO 735 Genes GS181962: GO:0016491 oxidoreductase activity
Expand Tier I Mouse GO 766 Genes GS186442: GO:0071822 protein complex subunit organization
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 4024 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human GO 1668 Genes GS202188: GO:0044248 cellular catabolic process
Expand Tier I Rat DRG 4920 Genes GS86494: Table S1: Hippocampus 17 K microarray data. [DRG]
Expand Tier I Human 490 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Mouse GO 1464 Genes GS182313: GO:0044085 cellular component biogenesis
Expand Tier I Human GO 28 Genes GS197166: GO:0030331 estrogen receptor binding
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
Expand Tier I Mouse GO 459 Genes GS182174: GO:0031966 mitochondrial membrane
Expand Tier I Mouse GO 3493 Genes GS177570: GO:0016043 cellular component organization
Expand Tier I Mouse GO 11 Genes GS186207: GO:0004303 estradiol 17-beta-dehydrogenase activity
Expand Tier I Human 592 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human GO 23 Genes GS197212: GO:0009081 branched-chain amino acid metabolic process
Expand Tier I Human 84 Genes GS174760: HP:0002376 Developmental regression
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human 13 Genes GS176058: HP:0002136 Broad-based gait
Expand Tier I Human GO 2764 Genes GS194555: GO:0031974 membrane-enclosed lumen
Expand Tier I Human GO 1 Genes GS206344: GO:0047015 3-hydroxy-2-methylbutyryl-CoA dehydrogenase activity
Expand Tier I Mouse GO 8414 Genes GS185585: GO:0044710 single-organism metabolic process
Expand Tier I Human GO 211 Genes GS204315: GO:0007568 aging
Expand Tier I Human GO 1281 Genes GS196726: GO:0005783 endoplasmic reticulum
Expand Tier I Human 398 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Human 489 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human GO 1165 Genes GS206696: GO:0044702 single organism reproductive process
Expand Tier I Mouse GO 128 Genes GS181657: GO:0016616 oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
Expand Tier III Mouse 398 Genes GS1140: Differential expression in brain of 22TNJ, a high alcohol-induced locomotor activation mutant
Expand Tier I Human GO 527 Genes GS198059: GO:0005740 mitochondrial envelope
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human GO 2511 Genes GS207903: GO:0044281 small molecule metabolic process
Expand Tier I Mouse 3289 Genes GS127932: Pallidum - Allen Mouse Brain Atlas
Expand Tier I Human 579 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Mouse GO 366 Genes GS185254: GO:0051259 protein oligomerization
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human GO 832 Genes GS194556: GO:0031975 envelope
Expand Tier I Human GO 994 Genes GS196927: GO:0065003 macromolecular complex assembly
Expand Tier I Human 34 Genes GS174909: HP:0000546 Retinal degeneration
Expand Tier I Human 472 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Mouse GO 726 Genes GS177814: GO:0031975 envelope
Expand Tier I Human 135 Genes GS172857: HP:0004305 Involuntary movements
Expand Tier I Mouse GO 590 Genes GS184446: GO:0044429 mitochondrial part
Expand Tier I Mouse GO 25 Genes GS187185: GO:0001540 beta-amyloid binding
Expand Tier I Human 699 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier III Mouse 107 Genes GS837: Sey_Pax6_Add_Up_Para
Expand Tier II Mouse 91 Genes GS34767: Whole Brain Gene expression correlates of Novel environment vertical activity counts minutes 45-60 in Females & Males BXD
Expand Tier I Human 512 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Mouse 301 Genes GS136883: testis weight (Tswt, Published QTL Chr X)
Expand Tier I Mouse GO 254 Genes GS185538: GO:0048037 cofactor binding
Expand Tier I Human 534 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Human 1985 Genes GS219747: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Human 334 Genes GS219678: http://www.broadinstitute.org/gsea/msigdb/cards/MITOCHONDRION
Expand Tier I Human GO 3513 Genes GS193991: GO:0048731 system development
Expand Tier I Human 114 Genes GS175593: HP:0011015 Abnormality of blood glucose concentration
Expand Tier I Mouse GO 1603 Genes GS177409: GO:0005739 mitochondrion
Expand Tier I Mouse 685 Genes GS128586: Rotarod Baseline Chr# X
Expand Tier III Mouse 41 Genes GS26277: Whole Brain Gene expression correlates of Mechanical Sensitivity-Von Frey Threshold [Pain] in Males BXD
Expand Tier I Human 161 Genes GS176803: HP:0001260 Dysarthria