Gene Details



C9orf72 and homologs in 4 species are found in 131 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 459 Genes GS129071: anticardiolipin antibody 2 (Acla2 Published QTL Chr 4)
Expand Tier I Human 64 Genes GS174310: HP:0100705 Abnormality of the glial cells
Expand Tier I Mouse 378 Genes GS136480: plasmacytoma susceptibility 2 (Pcyts2, Published QTL Chr 4)
Expand Tier I Human 832 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Mouse 325 Genes GS136209: lupus BXSB x NZW 1 (Lxw1, Published QTL Chr 4)
Expand Tier I Human 10 Genes GS173117: HP:0100660 Dyskinesia
Expand Tier I Mouse 365 Genes GS135944: HDL QTL 10 (Hdlq10, Published QTL Chr 4)
Expand Tier I Human 50 Genes GS173113: HP:0002186 Apraxia
Expand Tier I Mouse 348 Genes GS135284: "alcohol preference locus 8, female specific" (Alcp8, Published QTL Chr 4)
Expand Tier I Mouse 356 Genes GS135525: body weight QTL 9 (Bwtq9, Published QTL Chr 4)
Expand Tier III Human 3178 Genes GS137407: Supplementary Table 2. Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier I Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Human 86 Genes GS172908: HP:0002450 Abnormality of the motor neurons
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human 44 Genes GS171083: HP:0001328 Specific learning disability
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Mouse 325 Genes GS136959: weight adult 1 (Wta1, Published QTL Chr 4)
Expand Tier I Human 140 Genes GS174860: HP:0010549 Paralysis due to lesions of the principle motor tracts
Expand Tier I Mouse 365 Genes GS136394: organ weight 3 (Org3, Published QTL Chr 4)
Expand Tier I Human 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Mouse 362 Genes GS135796: ethanol induced low dose activation 4 (Elda4, Published QTL Chr 4)
Expand Tier I Human 50 Genes GS173812: HP:0000738 Hallucinations
Expand Tier I Human 17 Genes GS174555: HP:0002385 Paraparesis
Expand Tier I Mouse 285 Genes GS128590: Average rotarod training latency Chr# 4
Expand Tier I Human 203 Genes GS171621: HP:0100851 Abnormal emotion/affect behavior
Expand Tier I Human 7 Genes GS171450: HP:0000605 Supranuclear gaze palsy
Expand Tier I Mouse 350 Genes GS136311: NZB and NZW autoimmunity 2 (Nbwa2, Published QTL Chr 4)
Expand Tier I Human 3 Genes GS176095: HP:0007308 Extrapyramidal dyskinesia
Expand Tier I Human 15 Genes GS172584: HP:0000741 Apathy
Expand Tier I Mouse DRG 919 Genes provisional GS86984: Table S2: The data provided represent genes showing differential expression using ANOVA. A. Genes showing main effect of strain. [DRG]
Expand Tier I Human 5 Genes GS173428: HP:0007354 Amyotrophic lateral sclerosis
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Mouse 378 Genes GS136715: susceptibility to lung cancer 18 (Sluc18, Published QTL Chr 4)
Expand Tier I Human 6 Genes GS173637: HP:0002366 Abnormality of the lower motor neuron
Expand Tier I Mouse DRG 919 Genes provisional GS87378: Table S2: The data provided represent genes showing differential expression using ANOVA. (Whole Table) [DRG]
Expand Tier I Mouse 365 Genes GS136230: mandible length 4 (Manln4, Published QTL Chr 4)
Expand Tier I Human 37 Genes GS174302: HP:0000716 Depression
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human 530 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Mouse 459 Genes GS129186: silicosis susceptibility 1 (Slcs1 Published QTL Chr 4)
Expand Tier I Mouse 325 Genes GS136640: salmonella enteritidis susceptibility 8 (Ses8, Published QTL Chr 4)
Expand Tier I Mouse 365 Genes GS136287: modifier of polycystic kidney disease progression 1 (Mopkd1, Published QTL Chr 4)
Expand Tier II Mouse 351 Genes GS84155: METH responses for climbing (Published QTL, Chr 4)
Expand Tier I Human 168 Genes GS175668: HP:0007369 Atrophy/Degeneration affecting the cerebrum
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse 459 Genes GS129188: spermatogenesis defect 1 (Spmd1 Published QTL Chr 4)
Expand Tier I Mouse 359 Genes GS135467: blood pressure QTL 3 (Bpq3, Published QTL Chr 4)
Expand Tier III Mouse 8003 Genes GS213041: Expression profiles of aging in C57BL/6 mouse hippocampal tissue
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Mouse 370 Genes GS136965: weight loss response 3 (Wtlr3, Published QTL Chr 4)
Expand Tier I Mouse 378 Genes GS135376: body length 6 (Bdln6, Published QTL Chr 4)
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Mouse 325 Genes GS136868: triglyceride QTL 1 (Triglq1, Published QTL Chr 4)
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human GO 5948 Genes GS195199: GO:0005634 nucleus
Expand Tier I Human 202 Genes GS174764: HP:0007367 Atrophy/Degeneration affecting the central nervous system
Expand Tier I Human 136 Genes GS171855: HP:0000597 Ophthalmoparesis
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human 185 Genes GS173065: HP:0003679 Pace of progression
Expand Tier I Human 472 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Human 164 Genes GS174994: HP:0002059 Cerebral atrophy
Expand Tier I Human 399 Genes GS171100: HP:0000759 Abnormality of the peripheral nervous system
Expand Tier I Mouse 348 Genes GS135283: "alcohol preference locus 7, male specific" (Alcp7, Published QTL Chr 4)
Expand Tier I Human 7 Genes GS172173: HP:0002273 Tetraparesis
Expand Tier II Mouse 377 Genes GS84156: METH responses for body temperature (Published QTL, Chr 4)
Expand Tier I Human 50 Genes GS176914: HP:0002171 Gliosis
Expand Tier I Human 699 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human 346 Genes GS172989: HP:0001324 Muscle weakness
Expand Tier I Human 472 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human 42 Genes GS176071: HP:0010551 Paraplegia/paraparesis
Expand Tier I Mouse 364 Genes GS136239: macrophage-associated risk inflammatory factor 1 (Marif1, Published QTL Chr 4)
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier III Mouse 5726 Genes GS213077: Genes with suggestive difference in (PWD) vs (PB6F1 + B6PF1 + B6) comparison
Expand Tier I Mouse 378 Genes GS136620: sucrose consumption 1 (Scon1, Published QTL Chr 4)
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse 200 Genes GS129068: autoimmune aoritis in MRL mice 1 (Aaom1 Published QTL Chr 4)
Expand Tier I Human 543 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Mouse 459 Genes GS129177: splenomegaly-NZB x NZW 2 (Sbw2 Published QTL Chr 4)
Expand Tier I Human 3 Genes GS175955: HP:0002442 Dyscalculia
Expand Tier I Mouse 459 Genes GS129191: seizure susceptibility 2 (Szs2 Published QTL Chr 4)
Expand Tier III Mouse 936 Genes GS863: Differential expression across development in Sey Pax6 mutants and controls in an inverted-U (downward parabola).
Expand Tier I Mouse 362 Genes GS136775: synechia 1 (Synch1, Published QTL Chr 4)
Expand Tier I Human 6 Genes GS173865: HP:0002145 Frontotemporal dementia
Expand Tier I Human 21 Genes GS175360: HP:0002529 Neuronal loss in central nervous system
Expand Tier I Mouse 365 Genes GS135936: HDL level 36 (Hdl36, Published QTL Chr 4)
Expand Tier I Human 90 Genes GS171351: HP:0003581 Adult onset
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human 161 Genes GS176803: HP:0001260 Dysarthria
Expand Tier I Human 913 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Mouse 355 Genes GS135623: cholesterol 8 (Chol8, Published QTL Chr 4)
Expand Tier I Human GO 1697 Genes GS194905: GO:0008219 cell death
Expand Tier I Mouse 369 Genes GS136585: rapid eye movement sleep 1 (Remslp1, Published QTL Chr 4)
Expand Tier I Mouse 378 Genes GS136016: heart failure modifier 3 (Hrtfm3, Published QTL Chr 4)
Expand Tier I Human 25 Genes GS173064: HP:0003678 Rapidly progressive
Expand Tier I Human CTD 4389 Genes GS123768: Cyclosporine interacting genes (MeSH:D016572) in CTD
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Mouse 362 Genes GS135329: autoimmune renal vasculitis 1 (Arvm1, Published QTL Chr 4)
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 607 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human 38 Genes GS173459: HP:0001300 Parkinsonism
Expand Tier I Mouse 133 Genes GS135465: blood pressure QTL 22 (Bpq22, Published QTL Chr 4)
Expand Tier I Human 108 Genes GS176797: HP:0001268 Mental deterioration
Expand Tier I Mouse 359 Genes GS136067: immune response to AAV2 QTL 1 (Imraq1, Published QTL Chr 4)
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 73 Genes GS175408: HP:0002071 Abnormality of extrapyramidal motor function
Expand Tier I Mouse 363 Genes GS136744: spermatogenesis defect 2 (Spmd2, Published QTL Chr 4)
Expand Tier I Human 62 Genes GS174055: HP:0000726 Dementia
Expand Tier I Human 229 Genes GS175577: HP:0003202 Amyotrophy
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human GO 1699 Genes GS203755: GO:0016265 death
Expand Tier I Mouse 362 Genes GS136759: soft tissue heal 3 (Stheal3, Published QTL Chr 4)
Expand Tier I Human CTD 866 Genes GS126764: Calcitriol interacting genes (MeSH:D002117) in CTD
Expand Tier I Human 1006 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 12 Genes GS175877: HP:0007373 Atrophy/Degeneration involving motor neurons
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Mouse 333 Genes GS135304: angiogenesis due to FGF2 QTL 1 (Angfq1, Published QTL Chr 4)
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human 498 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Human 17 Genes GS172488: HP:0000746 Delusions
Expand Tier II Mouse 369 Genes GS84157: METH responses for chewing (Published QTL, Chr 4)
Expand Tier I Mouse 364 Genes GS135709: diabetes susceptibility QTL 6 (Dbsq6, Published QTL Chr 4)
Expand Tier I Human 316 Genes GS170825: HP:0002167 Neurological speech impairment
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment