Gene Details



SPATA7 and homologs in 6 species are found in 349 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 I Mouse GO 7755 Genes GS185131: GO:0044699 single-organism process
Expand Tier I Human 258 Genes GS232057: PC Geneset - "V$CREB_Q2" pathway genes
Expand Tier I Human 385 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Mouse 301 Genes GS136711: susceptibility to lung cancer 12 (Sluc12, Published QTL Chr 12)
Expand Tier II Human 703 Genes GS237881: [MeSH] Retinal Diseases : D012164
Expand Tier I Human 877 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human GO 7609 Genes GS201949: GO:0044699 single-organism process
Expand Tier II Human 22403 Genes GS244084: [MeSH] Phenotype : D010641
Expand Tier III Human 49 Genes GS221924: Capture panel of retinitis pigmentosa (RP) genes used to diagnose Chinese probands
Expand Tier III Rat 842 Genes GS224007: Urinary albumin excretion QTL 22 (Uae22 Published QTL Chr 6)
Expand Tier I Human 829 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 535 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Tier II Mouse 162 Genes GS33864: Striatum Gene expression correlates of Difference in distance traveled (cm) during the first five min (saline-ethanol) in Males BXD
Expand Tier I Mouse 344 Genes GS135735: delta power in slow-wave sleep 2 (Dps2, Published QTL Chr 12)
Expand Tier I Human 251 Genes GS227918: MSigDB Geneset - V$ER_Q6_02
Expand Tier I Human 248 Genes GS230204: MSigDB Geneset - V$T3R_Q6
Expand Tier II Human 70216 Genes GS235234: [MeSH] Biochemical Phenomena : D001669
Expand Tier III Human 3028 Genes GS137407: Supplementary Table 2. Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier II Human 31959 Genes GS237114: [MeSH] Regulatory Elements, Transcriptional : D050436
Expand Tier I Human 261 Genes GS230587: MSigDB Geneset - V$CREB_Q2
Expand Tier I Mouse 401 Genes GS135566: cytokine deficiency colitis susceptibility 8 (Cdcs8, Published QTL Chr 12)
Expand Tier I Human 267 Genes GS228307: MSigDB Geneset - V$CREB_Q4
Expand Tier I Mouse GO 23778 Genes GS193268: GO:0005575 cellular_component
Expand Tier II Human 4661 Genes GS238716: [MeSH] Genetic Linkage : D008040
Expand Tier I Mouse GO 123 Genes GS193046: GO:0050953 sensory perception of light stimulus
Expand Tier II Human 70252 Genes GS238030: [MeSH] Chemical Phenomena : D055598
Expand Tier I Human 120 Genes GS172358: HP:0003117 Abnormality of circulating hormone level
Expand Tier I Human GO 578 Genes GS195583: GO:0019953 sexual reproduction
Expand Tier I Human 156 Genes GS172363: HP:0004324 Increased body weight
Expand Tier I Human 598 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Human 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier II Human 1090 Genes GS238558: [MeSH] Tandem Repeat Sequences : D020080
Expand Tier I Human 144 Genes GS227123: MSigDB Geneset - CYTAGCAAY_UNKNOWN
Expand Tier I Human 191 Genes GS229803: MSigDB Geneset - GSE22886_NAIVE_CD8_TCELL_VS_MEMORY_TCELL_UP
Expand Tier I Human 782 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 636 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human 423 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Mouse 301 Genes GS135390: body growth early QTL 11 (Bgeq11, Published QTL Chr 12)
Expand Tier I Human 323 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier II Human 2184 Genes GS241321: [MeSH] Untranslated Regions : D020506
Expand Tier I Human 533 Genes GS229094: MSigDB Geneset - TGAYRTCA_V$ATF3_Q6
Expand Tier II Human 432 Genes GS236659: [MeSH] Codon, Terminator : D018388
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 136 Genes GS175674: HP:0007360 Aplasia/Hypoplasia of the cerebellum
Expand Tier I Human 262 Genes GS231708: PC Geneset - "V$CREB_01" pathway genes
Expand Human 195 Genes GS222320: Genes associated with high risk of intellectual disability.
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 736 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human 590 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human GO 204 Genes GS210485: GO:0007601 visual perception
Expand Tier II Human 9858 Genes GS242870: [MeSH] Polymorphism, Genetic : D011110
Expand Tier I Human 389 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Human 140 Genes GS174860: HP:0010549 Paralysis due to lesions of the principle motor tracts
Expand Tier II Human 37746 Genes GS240208: [MeSH] Amino Acid Sequence : D000595
Expand Tier I Mouse 537 Genes GS136679: skull morphology 18 (Skull18, Published QTL Chr 12)
Expand Tier III Rat 269 Genes GS223176: Blood pressure QTL 213 (Bp213 Published QTL Chr 6)
Expand Tier II Human 30100 Genes GS238002: [MeSH] Antisense Elements (Genetics) : D016375
Expand Tier I Human 342 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human GO 493 Genes GS209225: GO:0007600 sensory perception
Expand Tier II Mouse 417 Genes GS84266: METH responses for home cage activity (Published QTL, Chr 12)
Expand Tier III Rat 606 Genes GS224248: Ventilatory control QTL 5 (Vencon5 Published QTL Chr 6)
Expand Tier II Mouse 374 Genes GS83982: cocaine related behavior 13 (Cocrb13, Published QTL, Chr 12)
Expand Human 70 Genes GS221898: RetNet genes linked to retinitis pigmentosa (RP)
Expand Tier I Human 652 Genes GS227892: MSigDB Geneset - GTGACGY_V$E4F1_Q6
Expand Tier I Mouse 479 Genes GS136071: insulin QTL 10 (Insq10, Published QTL Chr 12)
Expand Tier I Human 413 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier I Human 103 Genes GS173741: HP:0100699 Scarring
Expand Tier II Human 61866 Genes GS235287: [MeSH] Proteins : D011506
Expand Tier I Human 397 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Human GO 501 Genes GS207582: GO:0007276 gamete generation
Expand Tier II Human 46864 Genes GS243659: [MeSH] RNA, Messenger : D012333
Expand Tier II Human 56846 Genes GS235305: [MeSH] DNA, Complementary : D018076
Expand Tier II Human 24839 Genes GS237194: [MeSH] Physiological Phenomena : D010829
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 1164 Genes GS206696: GO:0044702 single organism reproductive process
Expand Tier I Human 532 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier II Mouse 95 Genes GS26217: Neocortex Gene expression correlates of Thermal Nociception Hargreaves' Test in Females & Males BXD
Expand Tier I Human 489 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Mouse 359 Genes GS135368: B.burgdorferi-associated arthritis 6 (Bbaa6, Published QTL Chr 12)
Expand Tier II Human 39830 Genes GS245976: [MeSH] Cellular Structures : D022082
Expand Tier I Human 124 Genes GS175492: HP:0000512 Abnormal electroretinogram
Expand Tier II Human 67553 Genes GS240572: [MeSH] DNA : D004247
Expand Tier II Human 31495 Genes GS241930: [MeSH] Mutation : D009154
Expand Tier III Rat 706 Genes GS223844: Urinary albumin excretion QTL 33 (Uae33 Published QTL Chr 6)
Expand Tier I Human 532 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier II Human 20510 Genes GS237794: [MeSH] Oligodeoxyribonucleotides : D009838
Expand Tier II Human 43280 Genes GS236911: [MeSH] Transcription, Genetic : D014158
Expand Tier II Human 65203 Genes GS235942: [MeSH] Genetic Processes : D039361
Expand Tier I Human GO 637 Genes GS207720: GO:0048609 multicellular organismal reproductive process
Expand Tier II Human 849 Genes GS236202: [MeSH] Microsatellite Repeats : D018895
Expand Tier II Human 253 Genes GS236399: [MeSH] Consanguinity : D003241
Expand Tier I Human GO 5623 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 195 Genes GS227441: MSigDB Geneset - GSE22886_NAIVE_CD8_TCELL_VS_NKCELL_UP
Expand Tier I Human 384 Genes GS171708: HP:0000359 Abnormality of the inner ear
Expand Tier I Human 528 Genes GS231724: PC Geneset - "TGAYRTCA_V$ATF3_Q6" pathway genes
Expand Tier I Human 177 Genes GS171047: HP:0008736 Hypoplasia of penis
Expand Tier II Human 480 Genes GS235824: [MeSH] 5' Untranslated Regions : D020121
Expand Tier I Mouse 402 Genes GS136846: thymic lymphoma suppressor region 6 (Tlsr6, Published QTL Chr 12)
Expand Tier II Human 79329 Genes GS243722: [MeSH] Genetic Structures : D040342
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 Mouse 12 Genes GS36802: Whole Brain Gene expression correlates of Zero Maze - total time in open quadrants in Females BXD
Expand Tier I Human 280 Genes GS176231: HP:0010938 Abnormality of the external nose
Expand Tier I Human 89 Genes GS176988: HP:0008046 Abnormality of the retinal vasculature
Expand Tier II Human 59585 Genes GS234621: [MeSH] Chemical Actions and Uses : D020164
Expand Tier II Human 62071 Genes GS235061: [MeSH] Amino Acids, Peptides, and Proteins : D000602
Expand Tier I Human 401 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Human GO 393 Genes GS205650: GO:0048232 male gamete generation
Expand Tier II Human 1439 Genes GS235662: [MeSH] CpG Islands : D018899
Expand Tier II Human 8099 Genes GS236751: [MeSH] Polymorphism, Single Nucleotide : D020641
Expand Tier III Rat 842 Genes GS223840: Urinary albumin excretion QTL 37 (Uae37 Published QTL Chr 6)
Expand Tier I Human 171 Genes GS173019: HP:0000819 Diabetes mellitus
Expand Tier II Human 47536 Genes GS236298: [MeSH] Gene Expression : D015870
Expand Tier I Human 136 Genes GS171855: HP:0000597 Ophthalmoparesis
Expand Tier I Mouse 401 Genes GS135565: cytokine deficiency colitis susceptibility 7 (Cdcs7, Published QTL Chr 12)
Expand Tier I Human 122 Genes GS171946: HP:0002269 Abnormality of neuronal migration
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 Mouse 543 Genes GS135771: ear healing QTL 3 (Earheal3, Published QTL Chr 12)
Expand Tier II Human 36279 Genes GS241850: [MeSH] Genetic Variation : D014644
Expand Tier II Human 38809 Genes GS236076: [MeSH] Protein Conformation : D011487
Expand Tier II Human 19302 Genes GS236470: [MeSH] DNA-Binding Proteins : D004268
Expand Tier II Human 9078 Genes GS239596: [MeSH] Expressed Sequence Tags : D020224
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 III Rat 667 Genes GS223501: Urinary albumin excretion QTL 14 (Uae14 Published QTL Chr 6)
Expand Tier I Human 246 Genes GS231723: PC Geneset - "V$ER_Q6_02" pathway genes
Expand Tier III Rat 574 Genes GS224662: Pristane induced arthritis QTL 3 (Pia3 Published QTL Chr 6)
Expand Tier III Rat 706 Genes GS223777: Proteinuria QTL 8 (Pur8 Published QTL Chr 6)
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 I Human 541 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier III Rat 446 Genes GS224521: Anxiety related response QTL 28 (Anxrr28 Published QTL Chr 6)
Expand Tier I Human 510 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Mouse GO 5892 Genes GS180036: GO:0032501 multicellular organismal process
Expand Tier II Mouse 22 Genes GS36782: Whole Brain Gene expression correlates of Zero Maze - Time in Closed Arms in Females & Males BXD
Expand Tier III Rat 520 Genes GS224350: Anxiety related response QTL 5 (Anxrr5 Published QTL Chr 6)
Expand Tier I Human 532 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier II Human 50108 Genes GS239769: [MeSH] Gene Library : D015723
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 95 Genes GS176989: HP:0008047 Abnormality of the vasculature of the eye
Expand Tier I Mouse 438 Genes GS136123: life span 3 (Lifespan3, Published QTL Chr 12)
Expand Tier I Human 381 Genes GS175714: HP:0011389 Functional abnormality of the inner ear
Expand Tier I Mouse 301 Genes GS136064: immunoregulatory 6 (Im6, Published QTL Chr 12)
Expand Tier I Human CTD 530 Genes GS122992: nitrosobenzylmethylamine interacting genes (MeSH:C014707) in CTD
Expand Tier III Rat 433 Genes GS223175: Blood pressure QTL 212 (Bp212 Published QTL Chr 6)
Expand Tier II Human 83226 Genes GS241072: [MeSH] Genetic Phenomena : D055614
Expand Tier I Human 266 Genes GS231722: PC Geneset - "V$ER_Q6_01" pathway genes
Expand Tier II Human 60093 Genes GS243325: [MeSH] Base Sequence : D001483
Expand Tier II Human 158 Genes GS234599: [MeSH] Retinal Dystrophies : D058499
Expand Tier I Human 187 Genes GS171512: HP:0007703 Abnormal retinal pigmentation
Expand Tier II Human 20421 Genes GS237820: [MeSH] DNA Primers : D017931
Expand Tier II Human 24024 Genes GS240200: [MeSH] Transcription Initiation Site : D024363
Expand Tier I Human 413 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Mouse GO 6947 Genes GS192918: GO:0050896 response to stimulus
Expand Tier I Human 12 Genes GS174650: HP:0001133 Constricted visual fields
Expand Tier I Mouse GO 2138 Genes GS186067: GO:0050877 neurological system process
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 182 Genes GS176955: HP:0000431 Wide nasal bridge
Expand Tier I Human 198 Genes GS228912: MSigDB Geneset - GSE22886_CD8_VS_CD4_NAIVE_TCELL_UP
Expand Tier I Human 368 Genes GS170971: HP:0000407 Sensorineural hearing impairment
Expand Tier I Human 442 Genes GS175423: HP:0010461 Abnormality of the male genitalia
Expand Tier III Rat 350 Genes GS223475: Pristane induced arthritis QTL 24 (Pia24 Published QTL Chr 6)
Expand Tier I Human 267 Genes GS227233: MSigDB Geneset - V$ER_Q6_01
Expand Tier I Human 197 Genes GS227906: MSigDB Geneset - GSE3982_EOSINOPHIL_VS_EFF_MEMORY_CD4_TCELL_DN
Expand Tier I Mouse GO 2498 Genes GS193018: GO:0003008 system process
Expand Tier II Human 393 Genes GS239233: [MeSH] Codon, Nonsense : D018389
Expand Tier III Rat 570 Genes GS224675: Viral induced encephalitis QTL 3 (Vie3 Published QTL Chr 6)
Expand Tier I Human 120 Genes GS171657: HP:0000613 Photophobia
Expand Tier II Human 73736 Genes GS238575: [MeSH] Nucleic Acids : D009696
Expand Tier I Human 64 Genes GS172899: HP:0011815 Cephalocele
Expand Tier II Human 11815 Genes GS238961: [MeSH] Nerve Tissue Proteins : D009419
Expand Tier I Human 308 Genes GS172100: HP:0000587 Abnormality of the optic nerve
Expand Tier I Human 316 Genes GS175597: HP:0011013 Abnormality of carbohydrate metabolism/homeostasis
Expand Tier I Human 382 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Human GO 6548 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human 513 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human 230 Genes GS227979: MSigDB Geneset - TGACGTCA_V$ATF3_Q6
Expand Tier II Human 16 Genes GS238722: [MeSH] Leber Congenital Amaurosis : D057130
Expand Tier II Mouse 12 Genes GS36787: Whole Brain Gene expression correlates of Zero Maze - Time in Closed Arms in Females BXD
Expand Tier II Human 58261 Genes GS239502: [MeSH] Nucleic Acid Probes : D015341
Expand Tier I Human 197 Genes GS229990: MSigDB Geneset - GSE15659_NAIVE_CD4_TCELL_VS_NONSUPPRESSIVE_TCELL_DN
Expand Tier I Human 199 Genes GS176660: HP:0000050 Hypoplastic genitalia
Expand Tier I Human 260 Genes GS232035: PC Geneset - "V$CREB_Q4" pathway genes
Expand Tier I Mouse GO 23849 Genes GS180164: GO:0008150 biological_process
Expand Tier II Human 30111 Genes GS244835: [MeSH] Chromosomes : D002875
Expand Tier I Mouse 401 Genes GS136023: hereditary spherocytosis modifer 1 (Hsm1, Published QTL Chr 12)
Expand Tier I Human 381 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Human 917 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier II Human 52165 Genes GS242059: [MeSH] Cells : D002477
Expand Tier I Human 196 Genes GS228638: MSigDB Geneset - GSE29618_LAIV_VS_TIV_FLU_VACCINE_DAY7_MONOCYTE_UP
Expand Tier I Human 196 Genes GS229295: MSigDB Geneset - GSE3982_CENT_MEMORY_CD4_TCELL_VS_TH1_UP
Expand Tier I Mouse 401 Genes GS136424: pulmonary adenoma resistance 3 (Par3, Published QTL Chr 12)
Expand Tier II Human 161 Genes GS238585: [MeSH] Retinitis Pigmentosa : D012174
Expand Tier I Human 985 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier II Human 73996 Genes GS244482: [MeSH] Nucleic Acids, Nucleotides, and Nucleosides : D009706
Expand Tier I Human 609 Genes GS228458: MSigDB Geneset - WTGAAAT_UNKNOWN
Expand Tier I Mouse 438 Genes GS135873: femur geometry 10 (Fmgty10, Published QTL Chr 12)
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 Human 386 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Human 261 Genes GS229685: MSigDB Geneset - V$CREB_01
Expand Tier II Human 41481 Genes GS234192: [MeSH] Gene Expression Regulation : D005786
Expand Tier II Human 58023 Genes GS235242: [MeSH] Biochemical Processes : D055438
Expand Tier I Human 511 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Mouse 409 Genes GS135498: BSB obesity 4 (Bsbob4, Published QTL Chr 12)
Expand Tier II Human 52588 Genes GS245685: [MeSH] RNA : D012313
Expand Tier I Human GO 205 Genes GS209987: GO:0050953 sensory perception of light stimulus
Expand Tier I Mouse 408 Genes GS135978: wound healing/regeneration 5 (Heal5, Published QTL Chr 12)
Expand Tier II Human 1451 Genes GS238954: [MeSH] GC Rich Sequence : D020862
Expand Tier I Human 194 Genes GS228092: MSigDB Geneset - GSE15659_CD45RA_NEG_CD4_TCELL_VS_RESTING_TREG_DN
Expand Tier II Human 20860 Genes GS239302: [MeSH] Oligonucleotides : D009841
Expand Tier III Mouse 2256 Genes GS216489: Genes that are binding sites of CREB and zif268, transcription factors mediating neuronal activity and plasticity, in Mus musculus.
Expand Tier II Human 1026 Genes GS246010: [MeSH] Codon : D003062
Expand Tier I Human 64 Genes GS174379: HP:0002084 Encephalocele
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Mouse 389 Genes GS136450: postnatal body weight growth 12 (Pbwg12, Published QTL Chr 12)
Expand Tier I Human 42 Genes GS174449: HP:0001123 Visual field defect
Expand Tier I Human 220 Genes GS171791: HP:0000370 Abnormality of the middle ear
Expand Tier I Mouse 366 Genes GS136930: vertebral trabecular bone trait 14 (Vtbt14, Published QTL Chr 12)
Expand Tier I Human 411 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Mouse 199 Genes GS228724: MSigDB Geneset - GSE27786_LIN_NEG_VS_BCELL_UP
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 1222 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human 260 Genes GS227186: MSigDB Geneset - V$AFP1_Q6
Expand Tier I Mouse 359 Genes GS135226: antibody mediated myocarditis (Abmm, Published QTL Chr 12)
Expand Tier I Human 230 Genes GS232155: PC Geneset - "TGACGTCA_V$ATF3_Q6" pathway genes
Expand Tier II Human 3012 Genes GS234181: [MeSH] Retina : D012160
Expand Tier II Human 231 Genes GS235766: [MeSH] Chromosomes, Human, Pair 14 : D002883
Expand Tier I Human 288 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier I Human 1002 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier III Rat 495 Genes GS223695: Stress Responsive Cort QTL 4 (Srcrt4 Published QTL Chr 6)
Expand Tier II Human 630 Genes GS238471: [MeSH] Chromosomes, Human, 13-15 : D002901
Expand Tier III Rat 235 Genes GS224301: Insulin dependent diabetes mellitus QTL 18 (Iddm18 Published QTL Chr 6)
Expand Tier I Mouse 479 Genes GS135713: diabesity 3 (Dbsty3, Published QTL Chr 12)
Expand Tier I Mouse 537 Genes GS136399: organ weight 8 (Org8, Published QTL Chr 12)
Expand Tier I Human 256 Genes GS232439: PC Geneset - "V$CREBP1CJUN_01" pathway genes
Expand Tier III Rat 707 Genes GS224025: Urinary albumin excretion QTL 7 (Uae7 Published QTL Chr 6)
Expand Tier I Human 88 Genes GS230138: MSigDB Geneset - GGCCAGT,MIR-193A,MIR-193B
Expand Tier II Human 58766 Genes GS243866: [MeSH] Laboratory Chemicals : D019995
Expand Tier I Human 209 Genes GS173206: HP:0003241 Genital hypoplasia
Expand Tier I Human 157 Genes GS171968: HP:0000405 Conductive hearing impairment
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 158 Genes GS171900: HP:0011452 Functional abnormality of the middle ear
Expand Tier III Rat 406 Genes GS224339: Insulin dependent diabetes mellitus QTL 8 (Iddm8 Published QTL Chr 6)
Expand Tier I Mouse 302 Genes GS135531: Cyp7a1 mRNA level QTL (C7mlq, Published QTL Chr 12)
Expand Tier III Rat 605 Genes GS224361: Glomerulus QTL 8 (Glom8 Published QTL Chr 6)
Expand Tier II Human 58901 Genes GS243233: [MeSH] Specialty Uses of Chemicals : D020313
Expand Tier I Mouse 738 Genes GS128594: Average rotarod training latency Chr# 12
Expand Tier I Human 496 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier II Human 482 Genes GS235047: [MeSH] Retinal Degeneration : D012162
Expand Tier I Human 66 Genes GS173753: HP:0000510 Retinitis pigmentosa
Expand Tier I Human 413 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Human 62 Genes GS221933: Mutations of 60 known causative genes in 157 families with retinitis pigmentosa (RP) based on exome sequencing
Expand Tier II Human 36882 Genes GS236241: [MeSH] Protein Structure, Tertiary : D017434
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 886 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 184 Genes GS230814: MSigDB Geneset - GSE11864_CSF1_VS_CSF1_IFNG_IN_MAC_UP
Expand Tier I Human 209 Genes GS175990: HP:0000463 Anteverted nares
Expand Tier II Human 14570 Genes GS237160: [MeSH] Repetitive Sequences, Nucleic Acid : D012091
Expand Tier I Mouse 537 Genes GS135254: adiposity 6 (Adip6, Published QTL Chr 12)
Expand Tier III Mouse 174 Genes GS1072: ZM_ACTIVITY_Chr12_98.000000-112.000000
Expand Tier I Mouse 302 Genes GS135262: acute functional tolerance to ethanol QTL 1 (Afteq1, Published QTL Chr 12)
Expand Tier I Human 95 Genes GS176616: HP:0000662 Night blindness
Expand Tier II Human 7137 Genes GS234179: [MeSH] DNA, Intergenic : D021901
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier II Human 357 Genes GS237228: [MeSH] Eye Diseases, Hereditary : D015785
Expand Tier I Human 264 Genes GS232632: PC Geneset - "V$AFP1_Q6" pathway genes
Expand Tier II Human 5871 Genes GS237484: [MeSH] Congenital, Hereditary, and Neonatal Diseases and Abnormalities : D009358
Expand Tier II Human 73356 Genes GS238415: [MeSH] Genome Components : D040481
Expand Tier I Human 837 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier II Human 1689 Genes GS240795: [MeSH] Eye Diseases : D005128
Expand Tier I Human 273 Genes GS172516: HP:0001347 Hyperreflexia
Expand Tier I Mouse GO 1550 Genes GS192290: GO:0007600 sensory perception
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human 646 Genes GS232529: PC Geneset - "GTGACGY_V$E4F1_Q6" pathway genes
Expand Tier II Human 39556 Genes GS238930: [MeSH] Molecular Conformation : D008968
Expand Tier I Human 78 Genes GS172553: HP:0100689 Decreased corneal thickness
Expand Tier II Human 58262 Genes GS240750: [MeSH] Molecular Probes : D015335
Expand Tier I Human 200 Genes GS227386: MSigDB Geneset - GSE29618_PRE_VS_DAY7_POST_LAIV_FLU_VACCINE_MONOCYTE_DN
Expand Tier I Human 169 Genes GS230772: MSigDB Geneset - TAAYNRNNTCC_UNKNOWN
Expand Tier I Human GO 637 Genes GS196811: GO:0032504 multicellular organism reproduction
Expand Tier II Human 4244 Genes GS234130: [MeSH] Genetic Diseases, Inborn : D030342
Expand Tier I Human 77 Genes GS173703: HP:0000842 Hyperinsulinemia
Expand Tier I Human 97 Genes GS173091: HP:0004374 Hemiplegia/hemiparesis
Expand Tier II Human 55514 Genes GS238409: [MeSH] Gene Components : D040461
Expand Tier I Mouse 573 Genes GS129193: tibia bone quality traits 3 (Tbqt3 Published QTL Chr 12)
Expand Tier III Rat 714 Genes GS223178: Blood pressure QTL 211 (Bp211 Published QTL Chr 6)
Expand Tier II Human 4020 Genes GS237150: [MeSH] Eye : D005123
Expand Tier I Human GO 1235 Genes GS202899: GO:0050877 neurological system process
Expand Tier I Human 79 Genes GS175373: HP:0011486 Abnormality of corneal thickness
Expand Tier II Mouse 22 Genes GS36797: Whole Brain Gene expression correlates of Zero Maze - total time in open quadrants in Females & Males BXD
Expand Tier II Mouse 436 Genes GS84265: nicotine sensitivity (Published QTL, Chr 12)
Expand Tier I Human 576 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier III Rat 342 Genes GS223483: Mammary carcinoma susceptibility QTL 26 (Mcs26 Published QTL Chr 6)
Expand Tier I Human 435 Genes GS173024: HP:0000811 Abnormal external genitalia
Expand Tier II Human 8519 Genes GS243346: [MeSH] Chromosomes, Human : D002877
Expand Tier II Human 73890 Genes GS239190: [MeSH] Genome : D016678
Expand Tier I Mouse 401 Genes GS135680: Crhr1 transcript abundance QTL 2 (Crhr1taq2, Published QTL Chr 12)
Expand Tier I Mouse 438 Genes GS135608: circulating hormone level QTL 17 (Chlq17, Published QTL Chr 12)
Expand Tier I Human 271 Genes GS230601: MSigDB Geneset - V$ER_Q6
Expand Tier II Human 32928 Genes GS234668: [MeSH] Open Reading Frames : D016366
Expand Tier II Human 4961 Genes GS242610: [MeSH] Sense Organs : D012679
Expand Tier I Human 1203 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier II Human 13292 Genes GS238111: [MeSH] Genotype : D005838
Expand Tier I Mouse 196 Genes GS229800: MSigDB Geneset - GSE32423_CTRL_VS_IL7_MEMORY_CD8_TCELL_UP
Expand Tier I Human GO 1691 Genes GS209960: GO:0003008 system process
Expand Tier I Human 274 Genes GS172372: HP:0000648 Optic atrophy
Expand Tier I Mouse GO 123 Genes GS193540: GO:0007601 visual perception
Expand Tier I Mouse 409 Genes GS136274: multigenic obesity QTL 3 (Mobq3, Published QTL Chr 12)
Expand Tier I Human GO 1596 Genes GS207991: GO:0000003 reproduction
Expand Tier II Human 56931 Genes GS241744: [MeSH] DNA, Single-Stranded : D004277
Expand Tier I Human 274 Genes GS232428: PC Geneset - "V$ER_Q6" pathway genes
Expand Tier II Human 20981 Genes GS241565: [MeSH] Polynucleotides : D011119
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human 100 Genes GS176744: HP:0000987 Atypical scarring of skin
Expand Tier I Human GO 1591 Genes GS196196: GO:0022414 reproductive process
Expand Tier I Mouse GO 23359 Genes GS177356: GO:0003674 molecular_function
Expand Tier II Human 73218 Genes GS245795: [MeSH] Genes : D005796
Expand Tier I Human 201 Genes GS171631: HP:0008051 Abnormality of the retinal pigment epithelium
Expand Tier II Human 33265 Genes GS237679: [MeSH] Genetic Code : D005815
Expand Tier I Human 194 Genes GS229857: MSigDB Geneset - GSE3982_EFF_MEMORY_VS_CENT_MEMORY_CD4_TCELL_UP
Expand Tier I Human 85 Genes GS173666: HP:0005978 Type II diabetes mellitus
Expand Tier I Human 30 Genes GS229171: MSigDB Geneset - chr14q31
Expand Tier I Mouse 200 Genes GS230672: MSigDB Geneset - GSE11924_TFH_VS_TH1_CD4_TCELL_DN
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 392 Genes GS203862: GO:0007283 spermatogenesis
Expand Tier I Human 550 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Mouse 396 Genes GS135991: Hfe modifier 4 (Hfem4, Published QTL Chr 12)
Expand Tier I Human 258 Genes GS228752: MSigDB Geneset - V$CREBP1CJUN_01
Expand Tier I Mouse 344 Genes GS135681: Crh transcript abundance QTL 2 (Crhtaq2, Published QTL Chr 12)
Expand Tier II Human 22746 Genes GS237337: [MeSH] Nucleotides : D009711
Expand Tier I Human 469 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier II Human 9287 Genes GS243335: [MeSH] Chromosomes, Mammalian : D033481
Expand Tier II Human 30749 Genes GS236775: [MeSH] RNA, Untranslated : D022661
Expand Tier I Human 220 Genes GS171139: HP:0005288 Abnormality of the nares
Expand Tier II Human 283 Genes GS244540: [MeSH] Lod Score : D008126
Expand Tier I Human 614 Genes GS176171: HP:0001250 Seizures
Expand Human 54 Genes GS221925: Capture panel of retinitis pigmentosa (RP) genes used to diagnose Irish probands
Expand Tier I Mouse 433 Genes GS136529: prion disease incubation time 4 (Prdt4, Published QTL Chr 12)
Expand Tier I Human 148 Genes GS172295: HP:0001513 Obesity
Expand Tier II Human 28680 Genes GS238990: [MeSH] Mathematical Concepts : D055641
Expand Tier II Human 8327 Genes GS244452: [MeSH] Organ Specificity : D009928