Gene Details



PRPS1 and homologs in 7 species are found in 510 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 GO 7755 Genes GS185131: GO:0044699 single-organism process
Expand Tier I Mouse GO 2 Genes GS191168: GO:0034418 urate biosynthetic process
Expand Tier I Human GO 1682 Genes GS204629: GO:1901564 organonitrogen compound metabolic process
Expand Tier III Rat 642 Genes GS223551: Stress response QTL 1 (Stresp1 Published QTL Chr X)
Expand Tier I Human GO 1821 Genes GS205510: GO:0001883 purine nucleoside binding
Expand Tier I Human GO 70 Genes GS210441: GO:0072527 pyrimidine-containing compound metabolic process
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 63 Genes GS175213: HP:0003693 Distal amyotrophy
Expand Tier I Mouse GO 2260 Genes GS189855: GO:0043168 anion binding
Expand Tier I Human 99 Genes GS175130: HP:0000750 Delayed speech and language development
Expand Tier I Mouse GO 1822 Genes GS190997: GO:0044281 small molecule metabolic process
Expand Tier I Human 641 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 840 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human CTD 2422 Genes GS123265: Estradiol interacting genes (MeSH:D004958) in CTD
Expand Tier I Mouse GO 1774 Genes GS184984: GO:0032553 ribonucleotide binding
Expand Tier I Human 17 Genes GS171261: HP:0002149 Hyperuricemia
Expand Tier I Human GO 762 Genes GS206251: GO:0016301 kinase activity
Expand Tier I Mouse GO 1765 Genes GS183645: GO:0017076 purine nucleotide binding
Expand Tier I Mouse GO 198 Genes GS177654: GO:0006164 purine nucleotide biosynthetic process
Expand Tier I Human GO 207 Genes GS194391: GO:0006164 purine nucleotide biosynthetic process
Expand Tier III Human 728 Genes GS1229: Differential gene expression among Heroin Abusers
Expand Tier I Mouse GO 89 Genes GS183586: GO:0046390 ribose phosphate biosynthetic process
Expand Tier I Mouse GO 92 Genes GS193433: GO:0009163 nucleoside biosynthetic process
Expand Tier I Human 489 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Human 357 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Mouse GO 4619 Genes GS191019: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Human 782 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier II Mouse 57 Genes GS34286: Striatum Gene expression correlates of Activity in 30 second interval post 3rd tone shock pairing in Females BXD
Expand Tier I Human 58 Genes GS171880: HP:0003134 Abnormality of peripheral nerve conduction
Expand Tier I Human 13 Genes GS174063: HP:0100732 Pancreatic fibrosis
Expand Tier I Human 157 Genes GS171718: HP:0002808 Kyphosis
Expand Tier I Mouse GO 4353 Genes GS192017: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Human GO 2603 Genes GS196343: GO:0036094 small molecule binding
Expand Human 195 Genes GS222320: Genes associated with high risk of intellectual disability.
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Mouse GO 3080 Genes GS177265: GO:0048731 system development
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier II Mouse 35 Genes GS36756: Neocortex Gene expression correlates of Vocalization Threshold - shock intensity (mA) in Females BXD
Expand Tier I Mouse GO 3597 Genes GS188142: GO:0048856 anatomical structure development
Expand Tier I Human GO 13 Genes GS200684: GO:0046112 nucleobase biosynthetic process
Expand Tier I Mouse GO 6 Genes GS178136: GO:0004749 ribose phosphate diphosphokinase activity
Expand Tier I Human 273 Genes GS174338: HP:0002719 Recurrent infections
Expand Tier I Mouse GO 32 Genes GS183055: GO:0019003 GDP binding
Expand Tier I Mouse GO 4114 Genes GS193414: GO:0044249 cellular biosynthetic process
Expand Tier I Human GO 2410 Genes GS209108: GO:0000166 nucleotide binding
Expand Tier I Human 454 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Mouse GO 676 Genes GS181721: GO:0006163 purine nucleotide metabolic process
Expand Tier II Mouse 35 Genes GS36751: Neocortex Gene expression correlates of Vocalization Threshold - shock intensity (mA) in Females & Males BXD
Expand Tier I Mouse GO 1745 Genes GS188652: GO:0001882 nucleoside binding
Expand Tier I Human 186 Genes GS173355: HP:0002205 Recurrent respiratory infections
Expand Tier I Human 122 Genes GS173242: HP:0001337 Tremor
Expand Tier I Human 737 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 260 Genes GS170933: HP:0001288 Gait disturbance
Expand Tier I Human 27 Genes GS171008: HP:0011096 Peripheral demyelination
Expand Tier I Human 13 Genes GS174887: HP:0001344 Absent speech
Expand Tier I Human GO 1818 Genes GS201799: GO:0032550 purine ribonucleoside binding
Expand Tier I Mouse GO 28 Genes GS177566: GO:0009167 purine ribonucleoside monophosphate metabolic process
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human 317 Genes GS176591: HP:0001276 Hypertonia
Expand Tier I Human 401 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 196 Genes GS174756: HP:0011947 Respiratory tract infection
Expand Tier I Human 53 Genes GS173697: HP:0001319 Neonatal hypotonia
Expand Tier I Human 9 Genes GS172693: HP:0002445 Tetraplegia
Expand Tier I Mouse GO 251 Genes GS177568: GO:0009165 nucleotide biosynthetic process
Expand Tier I Mouse GO 2565 Genes GS192299: GO:0006793 phosphorus metabolic process
Expand Tier I Human 201 Genes GS175171: HP:0001315 Reduced tendon reflexes
Expand Tier I Human 128 Genes GS173093: HP:0004372 Reduced consciousness/confusion
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Human GO 5623 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 1079 Genes GS178401: GO:0019637 organophosphate metabolic process
Expand Tier I Mouse GO 25 Genes GS193710: GO:0009124 nucleoside monophosphate biosynthetic process
Expand Tier III Mouse 6189 Genes GS213074: Genes with suggestive difference in (B6PF1) vs (PB6F1 + B6 + PWD) comparison
Expand Tier III Mouse 7843 Genes GS213041: Expression profiles of aging in C57BL/6 mouse hippocampal tissue
Expand Tier I Mouse GO 26 Genes GS187699: GO:0009112 nucleobase metabolic process
Expand Tier I Mouse GO 4500 Genes GS186790: GO:0006725 cellular aromatic compound metabolic process
Expand Tier III Rat 371 Genes GS224101: Memory QTL 15 (Memor15 Published QTL Chr X)
Expand Tier II Mouse 65 Genes GS34725: Striatum Gene expression correlates of Novel environment rears 15-30 min in the periphery in Males BXD
Expand Tier I Human GO 5400 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Human 232 Genes GS170999: HP:0000082 Abnormality of renal physiology
Expand Tier I Human 2 Genes GS172310: HP:0001980 Megaloblastic bone marrow
Expand Tier I Human 171 Genes GS173019: HP:0000819 Diabetes mellitus
Expand Tier I Human 10 Genes GS172451: HP:0007210 Lower limb amyotrophy
Expand Tier I Mouse GO 17 Genes GS193709: GO:0009127 purine nucleoside monophosphate biosynthetic process
Expand Tier I Human GO 5764 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human CTD 6287 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human 401 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Human 17 Genes GS173375: HP:0010832 Abnormality of pain sensation
Expand Tier I Mouse GO 10879 Genes GS181473: GO:0005488 binding
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 263 Genes GS175823: HP:0002093 Respiratory insufficiency
Expand Tier I Mouse GO 5892 Genes GS180036: GO:0032501 multicellular organismal process
Expand Tier I Human GO 10 Genes GS206776: GO:0009113 purine nucleobase biosynthetic process
Expand Tier I Mouse GO 5103 Genes GS192512: GO:0003824 catalytic activity
Expand Tier I Mouse GO 1736 Genes GS180644: GO:0032549 ribonucleoside binding
Expand Tier III Rat 47 Genes GS14945: Upregulated gene expression in CNS of alcohol-preferring (iP) and non-alcohol preferring (iNP) rats.
Expand Tier I Human 780 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier II Mouse 135 Genes GS35430: Whole Brain Gene expression correlates of Distance traveled (cm) during the second five minute bin after saline in Females BXD
Expand Tier I Mouse GO 541 Genes GS182665: GO:0042278 purine nucleoside metabolic process
Expand Tier I Human GO 1722 Genes GS198004: GO:0007399 nervous system development
Expand Tier I Mouse GO 3 Genes GS188129: GO:0046101 hypoxanthine biosynthetic process
Expand Tier I Mouse GO 84 Genes GS180133: GO:0046129 purine ribonucleoside biosynthetic process
Expand Tier I Human GO 5 Genes GS194884: GO:0004749 ribose phosphate diphosphokinase activity
Expand Tier I Mouse GO 160 Genes GS179388: GO:0000287 magnesium ion binding
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 3603 Genes GS198456: GO:0019438 aromatic compound biosynthetic process
Expand Tier I Mouse GO 373 Genes GS191013: GO:0044283 small molecule biosynthetic process
Expand Tier I Human 53 Genes GS171305: HP:0012145 Abnormality of multiple cell lineages in the bone marrow
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 95 Genes GS174135: HP:0002015 Dysphagia
Expand Tier I Human 205 Genes GS176283: HP:0009830 Peripheral neuropathy
Expand Tier I Human GO 3902 Genes GS198323: GO:0046872 metal ion binding
Expand Tier I Mouse GO 207 Genes GS193490: GO:0072522 purine-containing compound biosynthetic process
Expand Tier I Human GO 4 Genes GS200386: GO:0046391 5-phosphoribose 1-diphosphate metabolic process
Expand Tier I Mouse GO 933 Genes GS178813: GO:0046983 protein dimerization activity
Expand Tier I Mouse GO 13 Genes GS184225: GO:0016208 AMP binding
Expand Tier I Human GO 42 Genes GS207105: GO:0006220 pyrimidine nucleotide metabolic process
Expand Tier III Mouse 8331 Genes GS128199: Alcohol Preference union of 86 Gene Sets
Expand Tier I Mouse GO 581 Genes GS189897: GO:0009116 nucleoside metabolic process
Expand Tier I Human GO 2374 Genes GS206737: GO:0043168 anion binding
Expand Tier III Rat 535 Genes GS224235: Collagen induced arthritis QTL 19 (Cia19 Published QTL Chr X)
Expand Tier I Mouse GO 354 Genes GS183592: GO:0032561 guanyl ribonucleotide binding
Expand Tier I Human 382 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Mouse GO 719 Genes GS193489: GO:0072521 purine-containing compound metabolic process
Expand Tier I Mouse 310 Genes GS136739: small testis weight 2 (Smtw2, Published QTL Chr X)
Expand Tier I Human GO 709 Genes GS210435: GO:0072521 purine-containing compound metabolic process
Expand Tier I Human 7 Genes GS173338: HP:0004369 Decreased purine levels
Expand Tier I Human GO 39 Genes GS194308: GO:0009161 ribonucleoside monophosphate metabolic process
Expand Tier I Mouse 299 Genes GS136144: lithogenic gene 4 (Lith4, Published QTL Chr X)
Expand Tier I Mouse GO 816 Genes GS191700: GO:0006753 nucleoside phosphate metabolic process
Expand Tier I Human 604 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human 160 Genes GS175806: HP:0001417 X-linked inheritance
Expand Tier I Human 160 Genes GS175556: HP:0011675 Arrhythmia
Expand Tier I Human 313 Genes GS176568: HP:0000486 Strabismus
Expand Tier I Human 469 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Mouse GO 33 Genes GS177571: GO:0009161 ribonucleoside monophosphate metabolic process
Expand Tier I Human GO 4 Genes GS209561: GO:0006015 5-phosphoribose 1-diphosphate biosynthetic process
Expand Tier I Human 27 Genes GS171447: HP:0000601 Hypotelorism
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human GO 5337 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier I Mouse GO 4218 Genes GS192073: GO:1901576 organic substance biosynthetic process
Expand Tier I Mouse GO 7644 Genes GS188399: GO:0044238 primary metabolic process
Expand Tier I Human 62 Genes GS172355: HP:0002460 Distal muscle weakness
Expand Tier I Human 511 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Mouse GO 49 Genes GS191479: GO:0042440 pigment metabolic process
Expand Tier I Mouse GO 4478 Genes GS184435: GO:0046483 heterocycle metabolic process
Expand Tier III Mouse 1993 Genes GS865: Sey_Pax6_Age_Reduced_Linear_Incr
Expand Tier I Human 229 Genes GS175577: HP:0003202 Amyotrophy
Expand Tier I Human GO 13 Genes GS206730: GO:0046415 urate metabolic process
Expand Tier I Human GO 39 Genes GS203278: GO:0006144 purine nucleobase metabolic process
Expand Tier I Mouse GO 2439 Genes GS179580: GO:0036094 small molecule binding
Expand Tier I Human GO 3714 Genes GS194038: GO:1901362 organic cyclic compound biosynthetic process
Expand Tier I Human GO 1496 Genes GS201792: GO:0032559 adenyl ribonucleotide binding
Expand Tier I Rat DRG 3886 Genes provisional GS86769: Table S2: HIPPOCAMPUS MGC MICROARRAY [DRG]
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human GO 2 Genes GS208080: GO:0034418 urate biosynthetic process
Expand Tier I Human CTD 4424 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 Mouse DRG 646 Genes provisional GS87421: Table S5: Lists of complete results of correlation analysis between the transcriptional response to morphine and opioid-related traits (Whole Table) [DRG]
Expand Tier I Human 411 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human 541 Genes GS174385: HP:0002088 Abnormality of the lung
Expand Tier I Human 27 Genes GS172613: HP:0003477 Peripheral axonal neuropathy
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 56 Genes GS174922: HP:0000762 Decreased nerve conduction velocity
Expand Tier I Mouse GO 4651 Genes GS177310: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Human GO 4 Genes GS204989: GO:0046100 hypoxanthine metabolic process
Expand Tier III Mouse 169 Genes GS821: UCSD_CEREBELLUM_Interaction_Geno_Age_Time_Pattern_No_Change_4th
Expand Tier I Human 1222 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Mouse GO 731 Genes GS193220: GO:0006082 organic acid metabolic process
Expand Tier I Human 33 Genes GS173067: HP:0000444 Convex nasal ridge
Expand Tier I Mouse GO 863 Genes GS177902: GO:0042802 identical protein binding
Expand Tier I Human 407 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human GO 1832 Genes GS205511: GO:0001882 nucleoside binding
Expand Tier I Mouse 288 Genes GS136623: Stem cell proliferation 11 (Scpro11, Published QTL Chr X)
Expand Tier I Human 1002 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier I Mouse GO 10 Genes GS178221: GO:0046033 AMP metabolic process
Expand Tier I Human GO 2364 Genes GS207365: GO:0005829 cytosol
Expand Tier I Human 139 Genes GS171000: HP:0000083 Renal insufficiency
Expand Tier I Human 158 Genes GS174814: HP:0001639 Hypertrophic cardiomyopathy
Expand Tier I Human 375 Genes GS176038: HP:0002795 Functional respiratory abnormality
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Mouse GO 1451 Genes GS180305: GO:0016310 phosphorylation
Expand Tier I Human 86 Genes GS174810: HP:0001635 Congestive heart failure
Expand Tier I Human CTD 1151 Genes GS121437: Fluorouracil interacting genes (MeSH:D005472) in CTD
Expand Tier I Mouse DRG 609 Genes provisional GS87381: Table S1: Additional data file 1 is a table listing the results of two-way ANOVA (FDR < 1%). (Whole Table) [DRG]
Expand Tier I Human 936 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human CTD 1593 Genes GS124695: arsenic trioxide interacting genes (MeSH:C006632) in CTD
Expand Tier I Mouse GO 36 Genes GS188768: GO:0046148 pigment biosynthetic process
Expand Tier I Human 496 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Mouse GO 17 Genes GS177573: GO:0009168 purine ribonucleoside monophosphate biosynthetic process
Expand Tier I Human GO 277 Genes GS205826: GO:1901293 nucleoside phosphate biosynthetic process
Expand Tier I Human 43 Genes GS176250: HP:0002788 Recurrent upper respiratory tract infections
Expand Tier I Human 521 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Mouse GO 551 Genes GS189900: GO:0009119 ribonucleoside metabolic process
Expand Tier I Human GO 7308 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 404 Genes GS173743: HP:0001999 Abnormal facial shape
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 60 Genes GS170970: HP:0000154 Wide mouth
Expand Tier I Mouse GO 905 Genes GS188061: GO:0016772 transferase activity, transferring phosphorus-containing groups
Expand Tier I Human 44 Genes GS176540: HP:0002721 Immunodeficiency
Expand Tier I Human GO 37 Genes GS210658: GO:0009124 nucleoside monophosphate biosynthetic process
Expand Tier III Rat 371 Genes GS224556: Memory QTL 1 (Memor1 Published QTL Chr X)
Expand Tier I Human GO 1500 Genes GS203649: GO:0030554 adenyl nucleotide binding
Expand Tier I Mouse GO 84 Genes GS189346: GO:0042451 purine nucleoside biosynthetic process
Expand Tier I Human 20 Genes GS176236: HP:0002307 Drooling
Expand Tier I Human 413 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier I Mouse GO 219 Genes GS179910: GO:0030246 carbohydrate binding
Expand Tier I Human 284 Genes GS175594: HP:0011014 Abnormal glucose homeostasis
Expand Tier I Mouse GO 5879 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Human 44 Genes GS174918: HP:0000764 Peripheral axonal degeneration
Expand Tier I Mouse GO 2981 Genes GS177761: GO:0044271 cellular nitrogen compound biosynthetic process
Expand Tier III Mouse 238 Genes GS835: Sey_Pax6_Add_Linear_Decrease
Expand Tier I Mouse GO 3605 Genes GS190682: GO:0007275 multicellular organismal development
Expand Tier I Human 886 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 315 Genes GS170825: HP:0002167 Neurological speech impairment
Expand Tier I Human 189 Genes GS174579: HP:0002031 Abnormality of the esophagus
Expand Tier I Human GO 58 Genes GS208406: GO:0042440 pigment metabolic process
Expand Tier I Human 259 Genes GS176172: HP:0001251 Ataxia
Expand Tier I Human 187 Genes GS174247: HP:0000539 Abnormality of refraction
Expand Tier I Mouse GO 354 Genes GS183053: GO:0019001 guanyl nucleotide binding
Expand Tier I Mouse GO 487 Genes GS187771: GO:1901566 organonitrogen compound biosynthetic process
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier II Mouse 59 Genes GS35445: Whole Brain Gene expression correlates of Distance traveled (cm) during the fourth five minute bin after saline in Females BXD
Expand Tier I Human GO 667 Genes GS198511: GO:0006163 purine nucleotide metabolic process
Expand Tier I Mouse GO 25 Genes GS184671: GO:0043531 ADP binding
Expand Tier I Mouse GO 518 Genes GS190496: GO:0009150 purine ribonucleotide metabolic process
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Mouse GO 1444 Genes GS184976: GO:0032559 adenyl ribonucleotide binding
Expand Tier I Human 90 Genes GS172611: HP:0003474 Sensory impairment
Expand Tier I Human 525 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human 837 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier III Rat 49 Genes GS14947: Differential expression of ethanol non-alcohol preferring (iNP) rats vs. inbred alcohol-preferring (iP) rats with greater expression iNP rats than in iP rats
Expand Tier I Human 34 Genes GS176240: HP:0010932 Abnormality of nucleobase metabolism
Expand Tier I Human 542 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Mouse GO 253 Genes GS188963: GO:1901293 nucleoside phosphate biosynthetic process
Expand Tier I Human 159 Genes GS175096: HP:0000286 Epicanthus
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 5928 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Mouse GO 6204 Genes GS184629: GO:0005515 protein binding
Expand Tier I Human 733 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human GO 809 Genes GS208636: GO:0006753 nucleoside phosphate metabolic process
Expand Tier I Human 46 Genes GS171759: HP:0002936 Distal sensory impairment
Expand Tier I Human CTD 5732 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
Expand Tier I Human 8 Genes GS173736: HP:0001997 Gout
Expand Tier I Human GO 856 Genes GS194645: GO:0042802 identical protein binding
Expand Tier I Human 83 Genes GS172024: HP:0001369 Arthritis
Expand Tier I Mouse GO 1724 Genes GS185881: GO:0035639 purine ribonucleoside triphosphate binding
Expand Tier I Human 97 Genes GS173091: HP:0004374 Hemiplegia/hemiparesis
Expand Tier I Human 27 Genes GS175179: HP:0001310 Dysmetria
Expand Tier I Human 317 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier III Rat 354 Genes GS223550: Stress response QTL 3 (Stresp3 Published QTL Chr X)
Expand Tier I Human 2 Genes GS171441: HP:0003157 Progressive axonal neuropathy with demyelinization on electroneurography
Expand Tier I Human 576 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human GO 1809 Genes GS202716: GO:0035639 purine ribonucleoside triphosphate binding
Expand Tier III Mouse 244 Genes GS830: UCSD_CEREBELLUM_Reduced_Age_Cub
Expand Tier I Human 598 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human 173 Genes GS173901: HP:0002007 Frontal bossing
Expand Tier I Human GO 4554 Genes GS196806: GO:0032502 developmental process
Expand Tier I Mouse GO 532 Genes GS187633: GO:0019693 ribose phosphate metabolic process
Expand Tier I Human 803 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Mouse GO 1398 Genes GS181215: GO:0007399 nervous system development
Expand Tier I Mouse GO 3 Genes GS192621: GO:0006015 5-phosphoribose 1-diphosphate biosynthetic process
Expand Tier I Human 529 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human GO 1718 Genes GS208734: GO:0016740 transferase activity
Expand Tier I Human GO 1851 Genes GS200446: GO:0017076 purine nucleotide binding
Expand Tier I Mouse GO 13 Genes GS186432: GO:0006144 purine nucleobase metabolic process
Expand Tier I Human GO 6743 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human 1203 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 10 Genes GS176338: HP:0003481 Segmental peripheral demyelination/remyelination
Expand Tier I Human GO 5120 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Tier I Mouse GO 78 Genes GS191136: GO:0009152 purine ribonucleotide biosynthetic process
Expand Tier I Human 2 Genes GS171246: HP:0003142 Excessive purine production
Expand Tier I Mouse GO 4286 Genes GS190949: GO:0009058 biosynthetic process
Expand Tier I Mouse GO 1733 Genes GS184983: GO:0032550 purine ribonucleoside binding
Expand Tier I Mouse 288 Genes GS135733: dietary obesity 7 (Dob7, Published QTL Chr X)
Expand Tier I Human 676 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human 21 Genes GS176207: HP:0003781 Excessive salivation
Expand Tier I Human 274 Genes GS172372: HP:0000648 Optic atrophy
Expand Tier I Mouse GO 2263 Genes GS192174: GO:0000166 nucleotide binding
Expand Tier I Mouse GO 3005 Genes GS177308: GO:1901362 organic cyclic compound biosynthetic process
Expand Tier I Human GO 1202 Genes GS194505: GO:1901135 carbohydrate derivative metabolic process
Expand Tier I Human GO 853 Genes GS209614: GO:0055086 nucleobase-containing small molecule metabolic process
Expand Tier I Human 56 Genes GS174179: HP:0002514 Cerebral calcification
Expand Tier I Mouse 223 Genes GS135779: exercise endurance QTL 1 (Eeq1, Published QTL Chr X)
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human 27 Genes GS176587: HP:0001271 Polyneuropathy
Expand Tier I Human GO 15151 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human 596 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Human 322 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier I Mouse GO 23359 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Human GO 4 Genes GS204988: GO:0046101 hypoxanthine biosynthetic process
Expand Tier I Human 341 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Mouse GO 4588 Genes GS177309: GO:1901363 heterocyclic compound binding
Expand Tier I Human 395 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 193 Genes GS174813: HP:0001638 Cardiomyopathy
Expand Tier I Human 3 Genes GS171618: HP:0003537 Hypouricemia
Expand Tier I Mouse GO 9049 Genes GS180166: GO:0008152 metabolic process
Expand Tier I Human 52 Genes GS171719: HP:0000787 Nephrolithiasis
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 112 Genes GS200385: GO:0046390 ribose phosphate biosynthetic process
Expand Tier I Human GO 2411 Genes GS203886: GO:1901265 nucleoside phosphate binding
Expand Tier I Human GO 646 Genes GS204631: GO:1901566 organonitrogen compound biosynthetic process
Expand Tier I Human 104 Genes GS171336: HP:0001732 Abnormality of the pancreas
Expand Tier I Mouse GO 4637 Genes GS177382: GO:0097159 organic cyclic compound binding
Expand Tier I Human 396 Genes GS171100: HP:0000759 Abnormality of the peripheral nervous system
Expand Tier I Human 31 Genes GS175341: HP:0100755 Abnormality of salivation
Expand Tier I Human 390 Genes GS175537: HP:0011277 Abnormality of the urinary system physiology
Expand Tier II Mouse 94 Genes GS36362: Whole Brain Gene expression correlates of Open Field - Total rears 0-5 minutes in Females & Males BXD
Expand Tier I Human 141 Genes GS172281: HP:0000822 Hypertension
Expand Tier I Mouse GO 1759 Genes GS184978: GO:0032555 purine ribonucleotide binding
Expand Tier I Human 344 Genes GS172989: HP:0001324 Muscle weakness
Expand Tier I Human 469 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Mouse GO 580 Genes GS177903: GO:0042803 protein homodimerization activity
Expand Tier I Human GO 273 Genes GS194305: GO:0009165 nucleotide biosynthetic process
Expand Tier I Mouse GO 987 Genes GS177766: GO:1901135 carbohydrate derivative metabolic process
Expand Tier I Mouse GO 3 Genes GS183587: GO:0046391 5-phosphoribose 1-diphosphate metabolic process
Expand Tier II Mouse 71 Genes GS36367: Whole Brain Gene expression correlates of Open Field - Total rears 0-5 minutes in Females BXD
Expand Tier I Human 583 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Mouse GO 1418 Genes GS188322: GO:0005524 ATP binding
Expand Tier I Human 776 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Mouse GO 92 Genes GS189349: GO:0042455 ribonucleoside biosynthetic process
Expand Tier I Human 614 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse GO 4073 Genes GS180034: GO:0032502 developmental process
Expand Tier I Human 143 Genes GS176586: HP:0001270 Motor delay
Expand Tier I Human 542 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human GO 1844 Genes GS201794: GO:0032555 purine ribonucleotide binding
Expand Tier I Mouse GO 362 Genes GS177764: GO:1901137 carbohydrate derivative biosynthetic process
Expand Tier I Human 173 Genes GS171148: HP:0011218 Abnormal shape of the frontal region
Expand Tier I Human GO 5347 Genes GS203642: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Human 621 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Human 381 Genes GS175714: HP:0011389 Functional abnormality of the inner ear
Expand Tier I Human GO 5567 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 120 Genes GS171607: HP:0011337 Abnormality of mouth size
Expand Tier I Human 40 Genes GS176115: HP:0000540 Hypermetropia
Expand Tier I Mouse GO 2507 Genes GS192296: GO:0006796 phosphate-containing compound metabolic process
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 6 Genes GS204917: GO:0016778 diphosphotransferase activity
Expand Tier I Human GO 5526 Genes GS194040: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Rat DRG 4750 Genes GS86932: Table S3: CORTEX 17K MICROARRAY [DRG]
Expand Tier I Human 413 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Human GO 1179 Genes GS195151: GO:0019637 organophosphate metabolic process
Expand Tier I Human 90 Genes GS171351: HP:0003581 Adult onset
Expand Tier I Mouse GO 2917 Genes GS190067: GO:0018130 heterocycle biosynthetic process
Expand Tier I Mouse GO 527 Genes GS191870: GO:0009259 ribonucleotide metabolic process
Expand Tier I Mouse GO 1449 Genes GS186798: GO:0030554 adenyl nucleotide binding
Expand Tier I Human 368 Genes GS170971: HP:0000407 Sensorineural hearing impairment
Expand Tier I Human 79 Genes GS171446: HP:0000600 Abnormality of the pharynx
Expand Tier I Human GO 2486 Genes GS209235: GO:0006793 phosphorus metabolic process
Expand Tier I Human 267 Genes GS172365: HP:0003110 Abnormality of urine homeostasis
Expand Tier I Human 87 Genes GS173938: HP:0001679 Abnormality of the aorta
Expand Tier I Human 2 Genes GS172823: HP:0003240 Increased phosphoribosylpyrophosphate (PRPP) synthetase
Expand Tier I Human GO 523 Genes GS204496: GO:0019693 ribose phosphate metabolic process
Expand Tier I Human 356 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Human 308 Genes GS172100: HP:0000587 Abnormality of the optic nerve
Expand Tier I Human GO 5014 Genes GS210357: GO:0044249 cellular biosynthetic process
Expand Tier I Human 316 Genes GS175597: HP:0011013 Abnormality of carbohydrate metabolism/homeostasis
Expand Tier I Mouse GO 7552 Genes GS180452: GO:0044237 cellular metabolic process
Expand Tier I Human GO 65 Genes GS204559: GO:0009112 nucleobase metabolic process
Expand Tier I Human 513 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human 50 Genes GS173052: HP:0000325 Triangular face
Expand Tier I Human 49 Genes GS171306: HP:0003130 Abnormal peripheral myelination
Expand Tier I Mouse GO 2991 Genes GS182469: GO:0043234 protein complex
Expand Tier I Mouse GO 5 Genes GS193174: GO:0006167 AMP biosynthetic process
Expand Tier I Human GO 966 Genes GS195570: GO:0046983 protein dimerization activity
Expand Tier I Human GO 3617 Genes GS206953: GO:0018130 heterocycle biosynthetic process
Expand Tier I Human 1046 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human GO 3697 Genes GS194499: GO:0044271 cellular nitrogen compound biosynthetic process
Expand Tier I Human CTD 4391 Genes GS123768: Cyclosporine interacting genes (MeSH:D016572) in CTD
Expand Tier I Mouse GO 23849 Genes GS180164: GO:0008150 biological_process
Expand Tier I Human 34 Genes GS172548: HP:0001522 Death in infancy
Expand Tier I Human 198 Genes GS174812: HP:0001637 Abnormality of the myocardium
Expand Tier I Human 917 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human GO 521 Genes GS194460: GO:0090407 organophosphate biosynthetic process
Expand Tier I Human GO 38 Genes GS210431: GO:0072528 pyrimidine-containing compound biosynthetic process
Expand Tier I Human 82 Genes GS175765: HP:0001419 X-linked recessive inheritance
Expand Tier I Human GO 1466 Genes GS205179: GO:0005524 ATP binding
Expand Tier I Human GO 8645 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 985 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Mouse GO 3583 Genes GS180236: GO:0032991 macromolecular complex
Expand Tier I Human 97 Genes GS176756: HP:0011420 Death
Expand Tier I Mouse GO 1411 Genes GS187769: GO:1901564 organonitrogen compound metabolic process
Expand Tier I Human GO 801 Genes GS206780: GO:0009117 nucleotide metabolic process
Expand Tier III Rat 409 Genes GS224100: Memory QTL 14 (Memor14 Published QTL Chr X)
Expand Tier I Mouse GO 86 Genes GS187546: GO:0009260 ribonucleotide biosynthetic process
Expand Tier I Human GO 2423 Genes GS209232: GO:0006796 phosphate-containing compound metabolic process
Expand Tier I Human 170 Genes GS173476: HP:0002311 Incoordination
Expand Tier I Human GO 549 Genes GS194503: GO:1901137 carbohydrate derivative biosynthetic process
Expand Tier I Human GO 786 Genes GS199922: GO:0005975 carbohydrate metabolic process
Expand Tier I Human GO 970 Genes GS210163: GO:0006082 organic acid metabolic process
Expand Tier I Human GO 5280 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Mouse GO 8072 Genes GS184218: GO:0071704 organic substance metabolic process
Expand Tier I Mouse GO 29 Genes GS193708: GO:0009126 purine nucleoside monophosphate metabolic process
Expand Tier I Rat DRG 3886 Genes provisional GS86945: Table S4: CORTEX MGC MICROARRAY [DRG]
Expand Tier I Human 95 Genes GS170930: HP:0001284 Areflexia
Expand Tier I Human 32 Genes GS172731: HP:0011463 Childhood onset
Expand Tier I Mouse GO 2855 Genes GS186757: GO:0034654 nucleobase-containing compound biosynthetic process
Expand Tier I Human 10 Genes GS173162: HP:0003323 Progressive muscle weakness
Expand Tier I Mouse GO 400 Genes GS177722: GO:0090407 organophosphate biosynthetic process
Expand Tier I Human GO 7609 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human GO 5184 Genes GS208954: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Human 829 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 535 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Tier III Rat 353 Genes GS224809: Glomerulus QTL 1 (Glom1 Published QTL Chr X)
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Mouse GO 3537 Genes GS192041: GO:0043169 cation binding
Expand Tier I Human 166 Genes GS171901: HP:0010985 Gonosomal inheritance
Expand Tier I Human 179 Genes GS175391: HP:0011004 Abnormality of the systemic arterial tree
Expand Tier I Human GO 434 Genes GS202416: GO:0044711 single-organism biosynthetic process
Expand Tier III Rat 985 Genes GS224236: Collagen induced arthritis QTL 18 (Cia18 Published QTL Chr X)
Expand Tier I Human 3 Genes GS171706: HP:0000791 Uric acid nephrolithiasis
Expand Tier I Human GO 46 Genes GS210654: GO:0009123 nucleoside monophosphate metabolic process
Expand Tier I Mouse DRG 609 Genes provisional GS86911: Table S1: Additional data file 1 is a table listing the results of two-way ANOVA (FDR < 1%). Lists of probe sets and gene names altered by morphine treatment (661). [DRG]
Expand Tier I Mouse GO 23778 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Human GO 5348 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Human GO 176 Genes GS196154: GO:0000287 magnesium ion binding
Expand Tier I Mouse GO 4887 Genes GS188190: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human 116 Genes GS173868: HP:0002143 Abnormality of the spinal cord
Expand Tier I Human GO 565 Genes GS194646: GO:0042803 protein homodimerization activity
Expand Tier I Mouse GO 385 Genes GS185586: GO:0044711 single-organism biosynthetic process
Expand Tier I Mouse DRG 646 Genes provisional GS86782: Table S5: Lists of complete results of correlation analysis between the transcriptional response to morphine and opioid-related traits [DRG]
Expand Tier I Human 372 Genes GS175815: HP:0011025 Abnormality of cardiovascular system physiology
Expand Tier I Human GO 4061 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human 86 Genes GS172908: HP:0002450 Abnormality of the motor neurons
Expand Tier I Human 24 Genes GS175065: HP:0004352 Abnormality of purine metabolism
Expand Tier I Human 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Mouse GO 7 Genes GS188059: GO:0016778 diphosphotransferase activity
Expand Tier I Human GO 4014 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human GO 1822 Genes GS197443: GO:0032549 ribonucleoside binding
Expand Tier I Mouse DRG 347 Genes provisional GS86515: Table S2: Additional data file 2 - Lists of probe sets of genes with expression altered by acute and chronic morphine (ANOVA; FDR < 1%). DBA/2J [DRG]
Expand Tier I Human 530 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier I Mouse GO 3 Genes GS188130: GO:0046100 hypoxanthine metabolic process
Expand Tier I Human 636 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Rat DRG 4750 Genes GS86494: Table S1: Hippocampus 17 K microarray data. [DRG]
Expand Tier I Mouse GO 11 Genes GS189848: GO:0046415 urate metabolic process
Expand Tier I Mouse GO 537 Genes GS180134: GO:0046128 purine ribonucleoside metabolic process
Expand Tier I Human GO 5190 Genes GS207857: GO:0009058 biosynthetic process
Expand Tier I Mouse GO 858 Genes GS192672: GO:0055086 nucleobase-containing small molecule metabolic process
Expand Tier I Human 3 Genes GS171239: HP:0003149 Hyperuricosuria
Expand Tier I Human GO 8948 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human GO 224 Genes GS210436: GO:0072522 purine-containing compound biosynthetic process
Expand Tier I Human CTD 2048 Genes GS127205: Tamoxifen interacting genes (MeSH:D013629) in CTD
Expand Tier I Human 590 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Mouse GO 3442 Genes GS181533: GO:0046872 metal ion binding
Expand Tier III 776 Genes GS213757: GenAge aging-associated genes in baker's yeast
Expand Tier I Human 484 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Mouse GO 39 Genes GS193706: GO:0009123 nucleoside monophosphate metabolic process
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human 140 Genes GS174860: HP:0010549 Paralysis due to lesions of the principle motor tracts
Expand Tier I Human 607 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human GO 3550 Genes GS203607: GO:0034654 nucleobase-containing compound biosynthetic process
Expand Tier I Human 12 Genes GS175367: HP:0002522 Areflexia of lower limbs
Expand Tier I Human 413 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier I Mouse GO 8414 Genes GS185585: GO:0044710 single-organism metabolic process
Expand Tier I Human 75 Genes GS173155: HP:0005561 Abnormality of bone marrow cell morphology
Expand Tier I Human 58 Genes GS171341: HP:0001739 Abnormality of the nasopharynx
Expand Tier I Human 17 Genes GS176514: HP:0007328 Impaired pain sensation
Expand Tier I Human CTD 109 Genes GS122740: hydroxytamoxifen interacting genes (MeSH:C475919) in CTD
Expand Tier I Human 397 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Human GO 4003 Genes GS208978: GO:0043169 cation binding
Expand Tier I Mouse GO 780 Genes GS189388: GO:0016301 kinase activity
Expand Tier I Human 487 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human GO 1859 Genes GS201800: GO:0032553 ribonucleotide binding
Expand Tier I Human 116 Genes GS170989: HP:0010766 Ectopic calcification
Expand Tier I Mouse GO 1736 Genes GS188651: GO:0001883 purine nucleoside binding
Expand Tier I Human 9 Genes GS171322: HP:0008944 Distal lower limb amyotrophy
Expand Tier I Human 33 Genes GS173194: HP:0012090 Abnormality of pancreas morphology
Expand Tier I Human DRG 868 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 9155 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human GO 30 Genes GS207107: GO:0006221 pyrimidine nucleotide biosynthetic process
Expand Tier I Human GO 2509 Genes GS207903: GO:0044281 small molecule metabolic process
Expand Tier I Human GO 9088 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human 47 Genes GS171072: HP:0000572 Visual loss
Expand Tier I Mouse GO 5225 Genes GS189860: GO:0043167 ion binding
Expand Tier I Human 17 Genes GS173339: HP:0004368 Increased purine levels
Expand Tier I Human 401 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Mouse GO 6 Genes GS189892: GO:0009113 purine nucleobase biosynthetic process
Expand Tier I Human 825 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Mouse GO 9 Genes GS183884: GO:0046112 nucleobase biosynthetic process
Expand Tier I Mouse GO 4 Genes GS192951: GO:0002189 ribose phosphate diphosphokinase complex
Expand Tier I Human 82 Genes GS172000: HP:0001761 Pes cavus
Expand Tier I Human 136 Genes GS171855: HP:0000597 Ophthalmoparesis
Expand Tier I Mouse GO 1686 Genes GS191796: GO:0016740 transferase activity
Expand Tier I Human GO 583 Genes GS206781: GO:0009116 nucleoside metabolic process