Gene Details



Hs.164682 and homologs in 7 species are found in 851 GeneSets:


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

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier II Human 2152 Genes GS234139: [MeSH] Biophysical Processes : D055597
Expand Tier I Human 19 Genes GS176512: HP:0004492 Widely patent fontanelles and sutures
Expand Tier III Human 1987 Genes GS246374: Differential Expression Hippocampi Human Cocaine Addicts
Expand Tier I Mouse GO 641 Genes GS185985: GO:0016818 hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides
Expand Tier II Human 2683 Genes GS242156: [MeSH] CHO Cells : D016466
Expand Tier I Human GO 1821 Genes GS205510: GO:0001883 purine nucleoside binding
Expand Tier III Rat 306 Genes GS224661: Pristane induced arthritis QTL 2 (Pia2 Published QTL Chr 4)
Expand Tier I Human 195 Genes GS228237: MSigDB Geneset - GSE18791_CTRL_VS_NEWCASTLE_VIRUS_DC_6H_UP
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Mouse GO 2260 Genes GS189855: GO:0043168 anion binding
Expand Tier II Human 8606 Genes GS243926: [MeSH] Exons : D005091
Expand Tier I Mouse GO 2 Genes GS189367: GO:0060151 peroxisome localization
Expand Tier I Human 99 Genes GS173687: HP:0001643 Patent ductus arteriosus
Expand Tier I Human 20 Genes GS175316: HP:0000565 Esotropia
Expand Tier II Human 14353 Genes GS244882: [MeSH] Epithelial Cells : D004847
Expand Tier I Human 94 Genes GS173846: HP:0003355 Aminoaciduria
Expand Tier I Human 60 Genes GS175897: HP:0000939 Osteoporosis
Expand Tier I Human 267 Genes GS172261: HP:0000357 Abnormal location of ears
Expand Tier I Human GO 2 Genes GS206231: GO:0060151 peroxisome localization
Expand Tier II Human 11812 Genes GS236947: [MeSH] Brain : D001921
Expand Tier I Human 641 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 318 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier I Human 840 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human 110 Genes GS171784: HP:0001399 Hepatic failure
Expand Tier I Mouse GO 1774 Genes GS184984: GO:0032553 ribonucleotide binding
Expand Tier II Human 70216 Genes GS235234: [MeSH] Biochemical Phenomena : D001669
Expand Tier I Mouse GO 404 Genes GS190247: GO:0032403 protein complex binding
Expand Tier I Human 148 Genes GS174586: HP:0005930 Abnormality of the epiphyses
Expand Tier II Human 31959 Genes GS237114: [MeSH] Regulatory Elements, Transcriptional : D050436
Expand Tier II Human 450 Genes GS244122: [MeSH] Leukoencephalopathies : D056784
Expand Tier III Rat 258 Genes GS225003: Glucose level QTL 4 (Gluco4 Published QTL Chr 4)
Expand Tier II Mouse 349 Genes GS35852: Striatum Gene expression correlates of Cocaine CPP - difference in time spent relative to baseline drug exposure in Males BXD
Expand Tier I Mouse GO 345 Genes GS185190: GO:0006605 protein targeting
Expand Tier II Human 11446 Genes GS236912: [MeSH] Biological Transport : D001692
Expand Tier II Human 10106 Genes GS234071: [MeSH] Protein Modification, Translational : D046188
Expand Tier I Mouse GO 1765 Genes GS183645: GO:0017076 purine nucleotide binding
Expand Tier II Human 15702 Genes GS245264: [MeSH] Nervous System : D009420
Expand Tier I Human 47 Genes GS173284: HP:0000311 Round face
Expand Tier I Human 178 Genes GS176151: HP:0000256 Macrocephaly
Expand Tier I Human 104 Genes GS176638: HP:0011603 Congenital malformation of the great arteries
Expand Tier I Human 146 Genes GS170968: HP:0000156 High-arched palate
Expand Tier I Human 489 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier II Human 19 Genes GS238683: [MeSH] Adrenoleukodystrophy : D000326
Expand Tier I Human 12 Genes GS174286: HP:0002570 Steatorrhea
Expand Tier II Human 1685 Genes GS241253: [MeSH] Protein Folding : D017510
Expand Tier I Human 135 Genes GS170969: HP:0000157 Abnormality of the tongue
Expand Tier I Mouse GO 46 Genes GS191431: GO:0031903 microbody membrane
Expand Tier I Human 147 Genes GS175411: HP:0100871 Abnormality of the palm
Expand Tier II Human 446 Genes GS245783: [MeSH] Genetic Diseases, X-Linked : D040181
Expand Tier III Rat 243 Genes GS223370: Subcutaneous fat weight QTL 2 (Scfw2 Published QTL Chr 4)
Expand Tier I Human 782 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Mouse 170 Genes GS136452: postnatal body weight growth 14 (Pbwg14, Published QTL Chr 5)
Expand Tier I Human 222 Genes GS173995: HP:0000508 Ptosis
Expand Tier I Human 223 Genes GS232643: PC Geneset - "V$CDPCR3HD_01" pathway genes
Expand Tier II Mouse 354 Genes GS84167: METH responses for home cage activity (Published QTL, Chr 5)
Expand Tier I Human 423 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Human 323 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier I Human 146 Genes GS176098: HP:0000927 Abnormality of skeletal maturation
Expand Tier I Human 66 Genes GS176033: HP:0011039 Abnormality of the helix
Expand Tier I Human 197 Genes GS229463: MSigDB Geneset - GSE3982_BASOPHIL_VS_TH2_UP
Expand Tier I Human 472 Genes GS171893: HP:0011458 Abdominal symptom
Expand Tier I Human GO 2603 Genes GS196343: GO:0036094 small molecule binding
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier II Human 906 Genes GS235249: [MeSH] Demyelinating Diseases : D003711
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
Expand Tier II Human 53 Genes GS239504: [MeSH] Hereditary Central Nervous System Demyelinating Diseases : D020279
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 736 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Mouse GO 385 Genes GS180235: GO:0007017 microtubule-based process
Expand Tier I Human GO 54 Genes GS209150: GO:0005778 peroxisomal membrane
Expand Tier I Human GO 786 Genes GS210137: GO:0016462 pyrophosphatase activity
Expand Tier I Mouse GO 8406 Genes GS177404: GO:0005737 cytoplasm
Expand Tier I Mouse GO 3493 Genes GS177570: GO:0016043 cellular component organization
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human CTD 2048 Genes GS127205: Tamoxifen interacting genes (MeSH:D013629) in CTD
Expand Tier I Human 282 Genes GS172060: HP:0001508 Failure to thrive
Expand Tier II Human 888 Genes GS239294: [MeSH] Heredodegenerative Disorders, Nervous System : D020271
Expand Tier I Human 590 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Mouse GO 3615 Genes GS178359: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human 84 Genes GS174760: HP:0002376 Developmental regression
Expand Tier I Human 300 Genes GS172416: HP:0002242 Abnormality of the intestine
Expand Tier I Human 116 Genes GS172063: HP:0000107 Renal cysts
Expand Tier I Human 48 Genes GS176364: HP:0008034 Abnormal iris pigmentation
Expand Tier I Mouse GO 1380 Genes GS185054: GO:0008104 protein localization
Expand Tier I Mouse GO 209 Genes GS190368: GO:0042623 ATPase activity, coupled
Expand Tier I Human 484 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier II Human 3578 Genes GS243730: [MeSH] Cytoplasmic Vesicles : D022162
Expand Tier I Mouse GO 4001 Genes GS183543: GO:0051179 localization
Expand Tier I Mouse GO 602 Genes GS178909: GO:0017111 nucleoside-triphosphatase activity
Expand Tier II Human 9858 Genes GS242870: [MeSH] Polymorphism, Genetic : D011110
Expand Tier I Human GO 421 Genes GS197015: GO:0007017 microtubule-based process
Expand Tier II Mouse 307 Genes GS35867: Striatum Gene expression correlates of Cocaine CPP - difference in percent test time spent relative to preconditioning in Males BXD
Expand Tier I Human 389 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Mouse GO 12 Genes GS193189: GO:0016558 protein import into peroxisome matrix
Expand Tier I Mouse GO 2762 Genes GS178357: GO:0071842 cellular component organization at cellular level
Expand Tier I Human 181 Genes GS175907: HP:0004349 Reduced bone mineral density
Expand Tier II Human 37746 Genes GS240208: [MeSH] Amino Acid Sequence : D000595
Expand Tier II Human 1868 Genes GS242884: [MeSH] 3' Untranslated Regions : D020413
Expand Tier II Human 21236 Genes GS240239: [MeSH] Sequence Homology : D017385
Expand Tier I Mouse 362 Genes GS136259: muscle Gapd decay rate 2 (Mgdr2, Published QTL Chr 5)
Expand Tier I Human 174 Genes GS171806: HP:0005656 Positional foot deformities
Expand Tier II Human 7666 Genes GS239503: [MeSH] Ubiquitination : D054875
Expand Tier I Human 70 Genes GS172568: HP:0000348 High forehead
Expand Tier II Human 268 Genes GS236097: [MeSH] Microbodies : D008830
Expand Tier I Human 112 Genes GS228054: MSigDB Geneset - HALLMARK_BILE_ACID_METABOLISM
Expand Tier II Human 30100 Genes GS238002: [MeSH] Antisense Elements (Genetics) : D016375
Expand Tier II Human 3807 Genes GS242661: [MeSH] Endocrine System Diseases : D004700
Expand Tier I Human 18 Genes GS172543: HP:0000835 Adrenal hypoplasia
Expand Tier I Human 104 Genes GS175835: HP:0007759 Opacification of the corneal stroma
Expand Tier I Human CTD 1454 Genes GS121893: Vitamin E interacting genes (MeSH:D014810) in CTD
Expand Tier I Human 342 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human 15 Genes GS175977: HP:0006579 Prolonged neonatal jaundice
Expand Tier I Human GO 2410 Genes GS209108: GO:0000166 nucleotide binding
Expand Tier II Human 2845 Genes GS244436: [MeSH] Gene Frequency : D005787
Expand Tier I Mouse GO 361 Genes GS187220: GO:0033365 protein localization to organelle
Expand Tier I Human 236 Genes GS174292: HP:0011968 Feeding difficulties
Expand Tier I Mouse 356 Genes GS135231: activity-distance traveled 2 (Actd2, Published QTL Chr 5)
Expand Tier II Human 35836 Genes GS242639: [MeSH] Metabolic Phenomena : D055754
Expand Tier II Human 9151 Genes GS238044: [MeSH] Acid Anhydride Hydrolases : D017766
Expand Tier I Human 35 Genes GS176655: HP:0000056 Abnormality of the clitoris
Expand Tier I Human GO 2 Genes GS206228: GO:0060152 microtubule-based peroxisome localization
Expand Tier I Human 454 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier III Rat 291 Genes GS224783: Plasma insulin-like growth factor 1 level QTL 3 (Pigfal3 Published QTL Chr 4)
Expand Tier I Human 607 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human 156 Genes GS176612: HP:0000272 Malar flattening
Expand Tier I Human 101 Genes GS171997: HP:0001762 Talipes equinovarus
Expand Tier I Mouse 359 Genes GS136365: obesity QTL 11 (Obq11, Published QTL Chr 5)
Expand Tier II Human 12291 Genes GS238872: [MeSH] Central Nervous System : D002490
Expand Tier I Mouse GO 175 Genes GS183468: GO:0008022 protein C-terminus binding
Expand Tier II Human 4837 Genes GS241025: [MeSH] Ribonucleotides : D012265
Expand Tier I Mouse GO 650 Genes GS191728: GO:0008289 lipid binding
Expand Tier II Human 27 Genes GS242623: [MeSH] Zellweger Syndrome : D015211
Expand Tier I Human 242 Genes GS175909: HP:0004348 Abnormality of bone mineral density
Expand Tier I Human GO 77 Genes GS205614: GO:0044438 microbody part
Expand Tier I Human 207 Genes GS174857: HP:0200006 Slanting of the palpebral fissure
Expand Tier II Human 4140 Genes GS235830: [MeSH] Cardiovascular Diseases : D002318
Expand Tier I Mouse GO 1745 Genes GS188652: GO:0001882 nucleoside binding
Expand Tier I Human 12 Genes GS175932: HP:0000244 Brachyturricephaly
Expand Tier I Human 346 Genes GS176615: HP:0000277 Abnormality of the mandible
Expand Tier I Human 175 Genes GS173048: HP:0005557 Abnormality of the zygomatic arch
Expand Tier II Human 1734 Genes GS238836: [MeSH] Metalloproteases : D045726
Expand Tier II Human 61866 Genes GS235287: [MeSH] Proteins : D011506
Expand Tier I Human 395 Genes GS173137: HP:0011821 Abnormality of facial skeleton
Expand Tier I Mouse GO 1366 Genes GS193632: GO:0051649 establishment of localization in cell
Expand Tier I Human 397 Genes GS172134: HP:0000639 Nystagmus
Expand Tier II Human 46864 Genes GS243659: [MeSH] RNA, Messenger : D012333
Expand Tier III Rat 174 Genes GS223644: Serum triglyceride level QTL 10 (Stl10 Published QTL Chr 4)
Expand Tier I Mouse GO 78 Genes GS189791: GO:0072594 establishment of protein localization to organelle
Expand Tier I Human 737 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 199 Genes GS229557: MSigDB Geneset - GSE18791_CTRL_VS_NEWCASTLE_VIRUS_DC_16H_UP
Expand Tier I Human 487 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Mouse GO 1209 Genes GS178284: GO:0031090 organelle membrane
Expand Tier II Human 15116 Genes GS243569: [MeSH] Macromolecular Substances : D046911
Expand Tier I Human GO 1818 Genes GS201799: GO:0032550 purine ribonucleoside binding
Expand Tier I Human GO 1859 Genes GS201800: GO:0032553 ribonucleotide binding
Expand Tier II Human 56846 Genes GS235305: [MeSH] DNA, Complementary : D018076
Expand Tier II Human 12802 Genes GS237481: [MeSH] Recombination, Genetic : D011995
Expand Tier II Human 8660 Genes GS239079: [MeSH] Cell Membrane : D002462
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier II Human 6533 Genes GS244610: [MeSH] Nervous System Diseases : D009422
Expand Tier I Human 116 Genes GS170989: HP:0010766 Ectopic calcification
Expand Tier I Human 532 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier II Human 7053 Genes GS235866: [MeSH] Amino Acids, Diamino : D000599
Expand Tier II Human 4450 Genes GS236040: [MeSH] Nutritional and Metabolic Diseases : D009750
Expand Tier I Human 18 Genes GS174615: HP:0004359 Abnormality of fatty-acid metabolism
Expand Tier II Human 2398 Genes GS238126: [MeSH] Integumentary System : D034582
Expand Tier II Mouse 118 Genes GS35904: Neocortex Gene expression correlates of Handling induced convulsions 4 hrs after ethanol in Females & Males BXD
Expand Tier I Human 76 Genes GS174649: HP:0000954 Single transverse palmar crease
Expand Tier I Human 11 Genes GS175604: HP:0005989 Redundant neck skin
Expand Tier I Human 489 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Human 178 Genes GS176589: HP:0001273 Abnormality of the corpus callosum
Expand Tier I Human 317 Genes GS176591: HP:0001276 Hypertonia
Expand Tier I Human 177 Genes GS229283: MSigDB Geneset - GSE9988_LPS_VS_LOW_LPS_MONOCYTE_DN
Expand Tier I Mouse GO 1736 Genes GS188651: GO:0001883 purine nucleoside binding
Expand Tier II Human 39830 Genes GS245976: [MeSH] Cellular Structures : D022082
Expand Tier I Human 124 Genes GS175492: HP:0000512 Abnormal electroretinogram
Expand Tier I Human 62 Genes GS176804: HP:0001850 Abnormality of the tarsal bones
Expand Tier II Human 67553 Genes GS240572: [MeSH] DNA : D004247
Expand Tier II Human 31495 Genes GS241930: [MeSH] Mutation : D009154
Expand Tier I Human 1871 Genes GS227896: MSigDB Geneset - TGGAAA_V$NFAT_Q4_01
Expand Tier III Rat 513 Genes GS224296: Renal function QTL 60 (Rf60 Published QTL Chr 4)
Expand Tier I Human 532 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier I Human 401 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 36 Genes GS174701: HP:0000556 Retinal dystrophy
Expand Tier I Human GO 19 Genes GS207128: GO:0072662 protein localization to peroxisome
Expand Tier II Human 1993 Genes GS238940: [MeSH] Urologic Diseases : D014570
Expand Tier II Human 16067 Genes GS239024: [MeSH] Cytoplasmic Structures : D022083
Expand Tier II Human 43280 Genes GS236911: [MeSH] Transcription, Genetic : D014158
Expand Tier I Mouse GO 46 Genes GS192217: GO:0005778 peroxisomal membrane
Expand Tier II Human 65203 Genes GS235942: [MeSH] Genetic Processes : D039361
Expand Tier I Human 201 Genes GS175171: HP:0001315 Reduced tendon reflexes
Expand Tier I Human 101 Genes GS177035: HP:0001928 Abnormality of coagulation
Expand Tier I Human GO 2104 Genes GS209928: GO:0006996 organelle organization
Expand Tier I Human 155 Genes GS176639: HP:0011356 Regional abnormality of skin
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Human 384 Genes GS171708: HP:0000359 Abnormality of the inner ear
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier II Human 15724 Genes GS239132: [MeSH] Gene Expression Regulation, Developmental : D018507
Expand Tier I Human 153 Genes GS175880: HP:0007370 Aplasia/Hypoplasia of the corpus callosum
Expand Tier I Human GO 167 Genes GS210585: GO:0051640 organelle localization
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier II Human 480 Genes GS235824: [MeSH] 5' Untranslated Regions : D020121
Expand Tier II Human 79329 Genes GS243722: [MeSH] Genetic Structures : D040342
Expand Tier I Mouse GO 17 Genes GS177096: GO:0006625 protein targeting to peroxisome
Expand Tier III Mouse 6189 Genes GS213074: Genes with suggestive difference in (B6PF1) vs (PB6F1 + B6 + PWD) comparison
Expand Tier II Human 67130 Genes GS241889: [MeSH] Molecular Structure : D015394
Expand Tier I Human 169 Genes GS173988: HP:0000501 Glaucoma
Expand Tier I Human 248 Genes GS176844: HP:0000429 Abnormality of the nasal alae
Expand Tier II Human 57 Genes GS242694: [MeSH] Peroxisomal Disorders : D018901
Expand Tier I Human 576 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier II Human 2242 Genes GS241209: [MeSH] Leupeptins : D007976
Expand Tier I Human 121 Genes GS175588: HP:0001311 Neurophysiological abnormality
Expand Tier II Human 8187 Genes GS234648: [MeSH] Alleles : D000483
Expand Tier I Human GO 9088 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human 280 Genes GS176231: HP:0010938 Abnormality of the external nose
Expand Tier I Human 15 Genes GS175060: HP:0001088 Brushfield spots
Expand Tier II Human 4098 Genes GS235532: [MeSH] Central Nervous System Diseases : D002493
Expand Tier II Human 3036 Genes GS241690: [MeSH] Female Urogenital Diseases : D052776
Expand Tier II Human 15 Genes GS243333: [MeSH] PHEX Phosphate Regulating Neutral Endopeptidase : D053402
Expand Tier I Mouse 356 Genes GS136236: mandible asymmetry 3 (Many3, Published QTL Chr 5)
Expand Tier I Human GO 20 Genes GS200896: GO:0043574 peroxisomal transport
Expand Tier II Human 59585 Genes GS234621: [MeSH] Chemical Actions and Uses : D020164
Expand Tier I Human GO 1965 Genes GS210586: GO:0051641 cellular localization
Expand Tier II Human 62071 Genes GS235061: [MeSH] Amino Acids, Peptides, and Proteins : D000602
Expand Tier III Rat 278 Genes GS223343: Hepatocarcinoma resistance QTL 13 (Hcar13 Published QTL Chr 4)
Expand Tier I Human 65 Genes GS174481: HP:0010576 Intracranial cystic lesion
Expand Tier I Human GO 5400 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Mouse GO 5225 Genes GS189860: GO:0043167 ion binding
Expand Tier II Human 3554 Genes GS244384: [MeSH] Female Urogenital Diseases and Pregnancy Complications : D005261
Expand Tier II Human 16797 Genes GS241667: [MeSH] Cytoplasm : D003593
Expand Tier I Human 262 Genes GS171645: HP:0011843 Abnormality of skeletal physiology
Expand Tier I Human 401 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Mouse GO 2190 Genes GS191129: GO:0016787 hydrolase activity
Expand Tier I Human 825 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Mouse GO 57 Genes GS188755: GO:0044438 microbody part
Expand Tier II Human 1439 Genes GS235662: [MeSH] CpG Islands : D018899
Expand Tier II Human 758 Genes GS236541: [MeSH] Cytoplasmic Granules : D003594
Expand Tier II Human 8099 Genes GS236751: [MeSH] Polymorphism, Single Nucleotide : D020641
Expand Tier I Human 10 Genes GS175077: HP:0001401 Intrahepatic biliary dysgenesis
Expand Tier II Human 23706 Genes GS235056: [MeSH] Peptides : D010455
Expand Tier II Human 47536 Genes GS236298: [MeSH] Gene Expression : D015870
Expand Tier II Human 6357 Genes GS243210: [MeSH] Lysine : D008239
Expand Tier I Human 55 Genes GS175055: HP:0001080 Biliary tract abnormality
Expand Tier I Human GO 5908 Genes GS195199: GO:0005634 nucleus
Expand Tier II Human 3287 Genes GS237404: [MeSH] Chromosomes, Human, 6-12 and X : D002906
Expand Tier I Human GO 4085 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human 169 Genes GS171752: HP:0001713 Abnormality of cardiac ventricle
Expand Tier I Human 280 Genes GS172572: HP:0000347 Micrognathia
Expand Tier I Human GO 4134 Genes GS200341: GO:0051179 localization
Expand Tier I Human GO 5764 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human 122 Genes GS171946: HP:0002269 Abnormality of neuronal migration
Expand Tier I Human 25 Genes GS176654: HP:0000057 Clitoromegaly
Expand Tier I Human 356 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Human 471 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Human 68 Genes GS176572: HP:0008064 Ichthyosiform abnormality of the skin
Expand Tier II Human 36279 Genes GS241850: [MeSH] Genetic Variation : D014644
Expand Tier I Human GO 794 Genes GS202828: GO:0016817 hydrolase activity, acting on acid anhydrides
Expand Tier II Human 1652 Genes GS237456: [MeSH] Kidney Diseases : D007674
Expand Tier I Mouse GO 17 Genes GS190231: GO:0072662 protein localization to peroxisome
Expand Tier II Human 38809 Genes GS236076: [MeSH] Protein Conformation : D011487
Expand Tier II Human 191 Genes GS239679: [MeSH] Adrenal Gland Diseases : D000307
Expand Tier II Human 15356 Genes GS234761: [MeSH] Reproductive Physiological Processes : D055704
Expand Tier II Human 4298 Genes GS241873: [MeSH] Glycoconjugates : D006001
Expand Tier I Human 199 Genes GS227128: MSigDB Geneset - GSE22886_NAIVE_CD4_TCELL_VS_12H_ACT_TH1_UP
Expand Tier I Human 361 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human CTD 6287 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier II Human 1039 Genes GS243748: [MeSH] Metabolism, Inborn Errors : D008661
Expand Tier III Mouse 171 Genes GS35878: Hippocampus Gene expression correlates of Number of entries into closed arms of plus maze [Ethanol] in Females BXD
Expand Tier I Mouse GO 30 Genes GS188256: GO:0007031 peroxisome organization
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 1068 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 695 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier II Human 3936 Genes GS245455: [MeSH] Metabolic Diseases : D008659
Expand Tier I Human 541 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier III Rat 1227 Genes GS224494: Blood pressure QTL 330 (Bp330 Published QTL Chr 4)
Expand Tier I Human 53 Genes GS175935: HP:0000248 Brachycephaly
Expand Tier I Mouse GO 10879 Genes GS181473: GO:0005488 binding
Expand Tier II Human 3784 Genes GS235626: [MeSH] Brain Diseases : D001927
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 510 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Human 263 Genes GS175823: HP:0002093 Respiratory insufficiency
Expand Tier III Rat 291 Genes GS223615: Anxiety related response QTL 48 (Anxrr48 Published QTL Chr 4)
Expand Tier II Human 7632 Genes GS241002: [MeSH] Amino Acids, Essential : D000601
Expand Tier I Mouse GO 5103 Genes GS192512: GO:0003824 catalytic activity
Expand Tier I Human 15 Genes GS176370: HP:0000262 Turricephaly
Expand Tier I Human 10 Genes GS172004: HP:0003455 Elevated long chain fatty acids
Expand Tier I Mouse GO 1736 Genes GS180644: GO:0032549 ribonucleoside binding
Expand Tier I Human GO 7717 Genes GS207616: GO:0016020 membrane
Expand Tier III Rat 467 Genes GS223647: Serum triglyceride level QTL 19 (Stl19 Published QTL Chr 4)
Expand Tier I Human 780 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 433 Genes GS175979: HP:0009115 Aplasia/Hypoplasia involving the skeleton
Expand Tier I Mouse 1585 Genes GS128591: Average rotarod training latency Chr# 5
Expand Tier I Human GO 19 Genes GS207127: GO:0072663 establishment of protein localization to peroxisome
Expand Tier I Human 231 Genes GS173288: HP:0000316 Hypertelorism
Expand Tier I Mouse GO 2 Genes GS189364: GO:0060152 microtubule-based peroxisome localization
Expand Tier I Human 56 Genes GS171030: HP:0010946 Dilatation of the renal pelvis
Expand Tier I Human GO 120 Genes GS209169: GO:0005777 peroxisome
Expand Tier I Human 66 Genes GS175160: HP:0002538 Abnormality of the cerebral cortex
Expand Tier I Human 532 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier II Human 50108 Genes GS239769: [MeSH] Gene Library : D015723
Expand Tier I Human 513 Genes GS229037: MSigDB Geneset - WTTGKCTG_UNKNOWN
Expand Tier II Human 58105 Genes GS242107: [MeSH] Chemical Processes : D055599
Expand Tier II Human 32929 Genes GS243578: [MeSH] Reading Frames : D016364
Expand Tier I Human 121 Genes GS172672: HP:0004337 Abnormality of amino acid metabolism
Expand Tier II Human 14459 Genes GS239072: [MeSH] Recombinant Proteins : D011994
Expand Tier I Human 263 Genes GS172415: HP:0002240 Hepatomegaly
Expand Tier II Human 29996 Genes GS237597: [MeSH] Cell Physiological Processes : D055648
Expand Tier I Mouse 200 Genes GS230089: MSigDB Geneset - GSE27786_BCELL_VS_ERYTHROBLAST_UP
Expand Tier I Human 46 Genes GS174388: HP:0002089 Pulmonary hypoplasia
Expand Tier I Human 300 Genes GS176029: HP:0009116 Aplasia/Hypoplasia involving bones of the skull
Expand Tier I Human 73 Genes GS176571: HP:0008067 Abnormally lax or hyperextensible skin
Expand Tier II Human 12085 Genes GS240544: [MeSH] Pregnancy : D011247
Expand Tier I Human 61 Genes GS175742: HP:0011733 Abnormality of adrenal physiology
Expand Tier I Human 309 Genes GS174899: HP:0100886 Abnormality of globe location
Expand Tier II Human 47 Genes GS238318: [MeSH] Adrenal Insufficiency : D000309
Expand Tier I Human 57 Genes GS171029: HP:0010944 Abnormality of the renal pelvis
Expand Tier I Human 121 Genes GS176695: HP:0009811 Abnormality of the elbow
Expand Tier III Rat 3415 Genes GS135132: bHR vs bLR genes different in Nucleus Acumbens
Expand Tier I Human 93 Genes GS228635: MSigDB Geneset - chr7q21
Expand Tier II Human 1833 Genes GS241820: [MeSH] Fatty Acids : D005227
Expand Mouse 99 Genes GS225469: Chronic cocaine mouse RNASeq NAc
Expand Tier I Human 125 Genes GS230126: MSigDB Geneset - chr7q11
Expand Tier I Human GO 499 Genes GS204077: GO:0033365 protein localization to organelle
Expand Tier II Human 23569 Genes GS235276: [MeSH] Signal Transduction : D015398
Expand Tier I Human 190 Genes GS227643: MSigDB Geneset - PIGF_UP.V1_UP
Expand Tier II Human 14819 Genes GS244426: [MeSH] Tumor Cells, Cultured : D014407
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier III Rat 3415 Genes GS135133: bHR vs bLR genes different in Hippocampus
Expand Tier I Human 205 Genes GS176283: HP:0009830 Peripheral neuropathy
Expand Tier II Human 2517 Genes GS246018: [MeSH] Heart Diseases : D006331
Expand Tier I Human 81 Genes GS171786: HP:0001396 Cholestasis
Expand Tier II Human 7823 Genes GS235095: [MeSH] Digestive System : D004064
Expand Tier I Mouse GO 939 Genes GS190471: GO:0005829 cytosol
Expand Tier I Human 250 Genes GS171634: HP:0008050 Abnormality of the palpebral fissures
Expand Tier I Human 33 Genes GS174910: HP:0000543 Optic disc pallor
Expand Tier II Human 13237 Genes GS241118: [MeSH] Binding Sites : D001665
Expand Tier I Human 222 Genes GS175459: HP:0009484 Deviation of the hand or of fingers of the hand
Expand Tier I Human 11 Genes GS174568: HP:0011040 Abnormality of the intrahepatic bile duct
Expand Tier I Human 187 Genes GS171167: HP:0000235 Abnormality of the fontanelles and cranial sutures
Expand Tier I Human 16 Genes GS171264: HP:0002630 Fat malabsorption
Expand Tier I Mouse GO 134 Genes GS192236: GO:0005777 peroxisome
Expand Tier III Mouse 8331 Genes GS128199: Alcohol Preference union of 86 Gene Sets
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Human GO 2374 Genes GS206737: GO:0043168 anion binding
Expand Tier II Human 12343 Genes GS236576: [MeSH] Promoter Regions, Genetic : D011401
Expand Tier II Human 350 Genes GS238362: [MeSH] Brain Diseases, Metabolic : D001928
Expand Tier II Human 413 Genes GS237651: [MeSH] Heart Valve Diseases : D006349
Expand Tier I Human 394 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human 60 Genes GS175162: HP:0002536 Abnormal cortical gyration
Expand Tier I Mouse GO 2872 Genes GS178360: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Human 70 Genes GS173601: HP:0010827 Abnormality of the seventh cranial nerve
Expand Tier I Human 194 Genes GS173872: HP:0011368 Epidermal thickening
Expand Tier II Human 58261 Genes GS239502: [MeSH] Nucleic Acid Probes : D015341
Expand Tier I Human 51 Genes GS172610: HP:0010864 Intellectual disability, severe
Expand Tier II Mouse 33 Genes GS34915: Whole Brain Gene expression correlates of Open Field - Total distance traveled 0-5 minutes in Males BXD
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier II Human 30111 Genes GS244835: [MeSH] Chromosomes : D002875
Expand Tier II Human 7624 Genes GS241772: [MeSH] Carbohydrates : D002241
Expand Tier I Human 233 Genes GS174257: HP:0000309 Abnormality of the midface
Expand Tier I Human 381 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier II Human 3385 Genes GS237069: [MeSH] Congenital Abnormalities : D000013
Expand Tier II Human 2834 Genes GS245072: [MeSH] Pseudogenes : D011544
Expand Tier I Human 20 Genes GS173959: HP:0001582 Redundant skin
Expand Tier I Human 136 Genes GS171202: HP:0100627 Displacement of the external urethral meatus
Expand Tier I Human 604 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human GO 77 Genes GS205613: GO:0044439 peroxisomal part
Expand Tier I Human GO 2361 Genes GS195036: GO:0031090 organelle membrane
Expand Tier I Human 219 Genes GS172288: HP:0000358 Posteriorly rotated ears
Expand Tier I Mouse GO 1598 Genes GS188957: GO:0033036 macromolecule localization
Expand Tier I Human 62 Genes GS174527: HP:0000952 Jaundice
Expand Tier I Human 160 Genes GS175556: HP:0011675 Arrhythmia
Expand Tier I Human 313 Genes GS176568: HP:0000486 Strabismus
Expand Tier II Human 73996 Genes GS244482: [MeSH] Nucleic Acids, Nucleotides, and Nucleosides : D009706
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 II Human 9240 Genes GS237965: [MeSH] Peptide Hydrolases : D010447
Expand Tier II Human 331 Genes GS240546: [MeSH] Brain Diseases, Metabolic, Inborn : D020739
Expand Tier I Human 17 Genes GS172788: HP:0000803 Renal cortical cysts
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier II Human 5171 Genes GS245493: [MeSH] Purines : D011687
Expand Tier I Human 514 Genes GS174081: HP:0004322 Short stature
Expand Tier I Mouse 83 Genes GS233522: KEGG Geneset - "Peroxisome" pathway genes
Expand Tier II Human 58105 Genes GS235797: [MeSH] DNA Probes : D015342
Expand Tier II Human 29719 Genes GS237296: [MeSH] RNA, Antisense : D016372
Expand Tier I Mouse 360 Genes GS136628: small effect CIA locus 1 (Secia1, Published QTL Chr 5)
Expand Tier I Mouse GO 134 Genes GS181579: GO:0042579 microbody
Expand Tier I Human 386 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier II Human 41481 Genes GS234192: [MeSH] Gene Expression Regulation : D005786
Expand Tier I Human 511 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier II Human 52588 Genes GS245685: [MeSH] RNA : D012313
Expand Tier I Human 229 Genes GS175577: HP:0003202 Amyotrophy
Expand Tier I Human 123 Genes GS175583: HP:0010438 Abnormality of the ventricular septum
Expand Tier II Human 10324 Genes GS234406: [MeSH] Multiprotein Complexes : D046912
Expand Tier II Human 1451 Genes GS238954: [MeSH] GC Rich Sequence : D020862
Expand Tier I Human GO 3402 Genes GS195113: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Mouse GO 133 Genes GS193638: GO:0051640 organelle localization
Expand Tier I Mouse GO 2439 Genes GS179580: GO:0036094 small molecule binding
Expand Tier I Human 34 Genes GS171863: HP:0008365 Abnormality of the talus
Expand Tier I Human GO 1496 Genes GS201792: GO:0032559 adenyl ribonucleotide binding
Expand Tier I Mouse GO 827 Genes GS180025: GO:0046907 intracellular transport
Expand Tier I Human 53 Genes GS170905: HP:0004400 Abnormality of the pylorus
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier II Human 13987 Genes GS237817: [MeSH] Cell Line, Tumor : D045744
Expand Tier I Mouse GO 1686 Genes GS184220: GO:0071702 organic substance transport
Expand Tier I Human 260 Genes GS172033: HP:0000369 Low-set ears
Expand Tier II Human 2308 Genes GS237932: [MeSH] Skin : D012867
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 II Human 376 Genes GS244358: [MeSH] Aortic Valve Stenosis : D001024
Expand Tier I Human 197 Genes GS227214: MSigDB Geneset - GSE3982_DC_VS_BASOPHIL_DN
Expand Tier II Human 28877 Genes GS238592: [MeSH] Cells, Cultured : D002478
Expand Tier I Human 81 Genes GS171773: HP:0000532 Chorioretinal abnormality
Expand Tier III Rat 276 Genes GS223577: Body weight QTL2 (Bw2 Published QTL Chr 4)
Expand Tier I Human 411 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human 82 Genes GS172098: HP:0000582 Upslanted palpebral fissure
Expand Tier I Human 92 Genes GS171656: HP:0000610 Abnormality of the choroid
Expand Tier I Human 541 Genes GS174385: HP:0002088 Abnormality of the lung
Expand Tier I Human 31 Genes GS173968: HP:0008207 Primary adrenal insufficiency
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human GO 354 Genes GS208384: GO:0016887 ATPase activity
Expand Tier II Human 3413 Genes GS245483: [MeSH] Male Urogenital Diseases : D052801
Expand Tier I Human 1222 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Mouse GO 263 Genes GS191457: GO:0016887 ATPase activity
Expand Tier I Human 70 Genes GS177025: HP:0010628 Facial palsy
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Human 132 Genes GS171835: HP:0011329 Abnormality of cranial sutures
Expand Tier I Human 550 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human 407 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human 16 Genes GS175019: HP:0001623 Breech presentation
Expand Tier I Human GO 1832 Genes GS205511: GO:0001882 nucleoside binding
Expand Tier I Human GO 158 Genes GS200264: GO:0008022 protein C-terminus binding
Expand Tier I Mouse GO 5247 Genes GS178448: GO:0005634 nucleus
Expand Tier II Human 23211 Genes GS235538: [MeSH] Protein Binding : D011485
Expand Tier I Human 288 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier II Human 8081 Genes GS245560: [MeSH] Ubiquitin : D025801
Expand Tier I Human 11 Genes GS171425: HP:0002416 Subependymal cysts
Expand Tier I Human 1002 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human 28 Genes GS176794: HP:0002967 Cubitus valgus
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier II Human 10133 Genes GS235960: [MeSH] Connective Tissue Cells : D003239
Expand Tier II Human 6306 Genes GS235691: [MeSH] Multienzyme Complexes : D009097
Expand Tier II Human 10298 Genes GS238960: [MeSH] Membrane Glycoproteins : D008562
Expand Tier I Human 486 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human 56 Genes GS175070: HP:0000973 Cutis laxa
Expand Tier I Human GO 2364 Genes GS207365: GO:0005829 cytosol
Expand Tier I Human 283 Genes GS175125: HP:0000028 Cryptorchidism
Expand Tier III Rat 104 Genes GS224177: Body weight QTL 144 (Bw144 Published QTL Chr 4)
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 1157 Genes GS228342: MSigDB Geneset - GATTGGY_V$NFY_Q6_01
Expand Tier I Human 105 Genes GS175571: HP:0011492 Abnormality of corneal stroma
Expand Tier II Human 4906 Genes GS239789: [MeSH] Adenosine Triphosphatases : D000251
Expand Tier II Human 650 Genes GS243363: [MeSH] Polymorphism, Single-Stranded Conformational : D018807
Expand Tier II Human 1649 Genes GS242013: [MeSH] Gene Duplication : D020440
Expand Tier III Mouse 8151 Genes GS213076: Genes with suggestive difference in (B6) vs (B6PF1 + PB6F1 + PWD) comparison
Expand Tier II Human 4900 Genes GS245843: [MeSH] Proteasome Endopeptidase Complex : D046988
Expand Tier I Human GO 1123 Genes GS196794: GO:0046907 intracellular transport
Expand Tier II Human 58766 Genes GS243866: [MeSH] Laboratory Chemicals : D019995
Expand Tier I Human 12202 Genes GS232685: PC Geneset - "Homo sapiens" pathway genes
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 II Human 15342 Genes GS242876: [MeSH] Proteome : D020543
Expand Tier I Human 99 Genes GS171649: HP:0011849 Abnormal bone ossification
Expand Tier I Mouse GO 17 Genes GS184095: GO:0043574 peroxisomal transport
Expand Tier I Mouse 360 Genes GS136070: immune response to Factor IX QTL 1 (Imrfq1, Published QTL Chr 5)
Expand Tier I Mouse 252 Genes GS136042: insulin dependent diabetes susceptibility 15 (Idd15, Published QTL Chr 5)
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human 10 Genes GS171161: HP:0004734 Renal cortical microcysts
Expand Tier II Human 5168 Genes GS244578: [MeSH] Liver : D008099
Expand Tier I Human 187 Genes GS176449: HP:0001671 Abnormality of the cardiac septa
Expand Tier I Human 243 Genes GS176694: HP:0009810 Abnormality of the joints of the upper limbs
Expand Tier II Human 58901 Genes GS243233: [MeSH] Specialty Uses of Chemicals : D020313
Expand Tier I Human 199 Genes GS228459: MSigDB Geneset - GSE360_LOW_DOSE_B_MALAYI_VS_M_TUBERCULOSIS_DC_DN
Expand Tier I Human 21 Genes GS175210: HP:0010537 Wide cranial sutures
Expand Tier I Human 496 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Human GO 6347 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human 233 Genes GS230280: MSigDB Geneset - V$CDPCR3HD_01
Expand Tier III Rat 291 Genes GS224080: Body weight QTL 155 (Bw155 Published QTL Chr 4)
Expand Tier I Human 521 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier II Human 2584 Genes GS235299: [MeSH] Physical Processes : D055586
Expand Tier I Human GO 7308 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 113 Genes GS173647: HP:0012072 Aciduria
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 66 Genes GS173753: HP:0000510 Retinitis pigmentosa
Expand Tier I Human 11 Genes GS174890: HP:0001341 Olfactory lobe agenesis
Expand Tier I Human 468 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier I Human 213 Genes GS176973: HP:0001072 Thickened skin