Gene Details



CHMP2B and homologs in 1 species are found in 136 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 Human GO 406 Genes GS199582: GO:0016044 cellular membrane organization
Expand Tier I Human 64 Genes GS174310: HP:0100705 Abnormality of the glial cells
Expand Tier I Human 201 Genes GS175171: HP:0001315 Reduced tendon reflexes
Expand Tier I Human 829 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Human GO 1745 Genes GS210579: GO:0051649 establishment of localization in cell
Expand Tier I Human 3 Genes GS172299: HP:0002483 Bulbar signs
Expand Tier I Human 10 Genes GS173117: HP:0100660 Dyskinesia
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 3 Genes GS172560: HP:0000743 Frontal release signs
Expand Tier I Human 168 Genes GS175668: HP:0007369 Atrophy/Degeneration affecting the cerebrum
Expand Tier I Human GO 9526 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human GO 1692 Genes GS203755: GO:0016265 death
Expand Tier I Human 9 Genes GS171971: HP:0002300 Mutism
Expand Tier I Human GO 6256 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 15151 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 9088 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human GO 80 Genes GS202907: GO:0031902 late endosome membrane
Expand Tier I Human 60 Genes GS174300: HP:0000718 Aggressive behavior
Expand Tier I Human GO 1965 Genes GS210586: GO:0051641 cellular localization
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human 11 Genes GS173817: HP:0000734 Disinhibition
Expand Tier I Human 840 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human 17 Genes GS172163: HP:0000711 Restlessness
Expand Tier I Human 1002 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human 30 Genes GS176897: HP:0002354 Memory impairment
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 825 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human 36 Genes GS173618: HP:0002747 Respiratory insufficiency due to muscle weakness
Expand Tier I Human GO 410 Genes GS201052: GO:0061024 membrane organization
Expand Tier I Human 95 Genes GS171217: HP:0003487 Babinski sign
Expand Tier I Human GO 2364 Genes GS207365: GO:0005829 cytosol
Expand Tier I Human 375 Genes GS176038: HP:0002795 Functional respiratory abnormality
Expand Tier I Human GO 5908 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 GO 4085 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 4134 Genes GS200341: GO:0051179 localization
Expand Tier I Human 185 Genes GS173065: HP:0003679 Pace of progression
Expand Tier I Human GO 1123 Genes GS196794: GO:0046907 intracellular transport
Expand Tier I Human 164 Genes GS174994: HP:0002059 Cerebral atrophy
Expand Tier I Human GO 153 Genes GS210474: GO:0005770 late endosome
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human 135 Genes GS172857: HP:0004305 Involuntary movements
Expand Tier I Human 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 311 Genes GS204442: GO:0010008 endosome membrane
Expand Tier I Human 396 Genes GS171100: HP:0000759 Abnormality of the peripheral nervous system
Expand Tier I Human 93 Genes GS176289: HP:0002120 Cerebral cortical atrophy
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human 5 Genes GS174303: HP:0000710 Hyperorality
Expand Tier I Human 263 Genes GS173014: HP:0010936 Abnormality of the lower urinary tract
Expand Tier I Human GO 539 Genes GS199393: GO:0019904 protein domain specific binding
Expand Tier I Human GO 1555 Genes GS201869: GO:0008104 protein localization
Expand Tier I Human 136 Genes GS175524: HP:0000009 Functional abnormality of the bladder
Expand Tier I Human 496 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Human 695 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human GO 6347 Genes GS201256: GO:0044422 organelle part
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 Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 521 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Human GO 938 Genes GS194065: GO:0016192 vesicle-mediated transport
Expand Tier I Human 144 Genes GS175754: HP:0000014 Abnormality of the bladder
Expand Tier I Human GO 7308 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 4 Genes GS171360: HP:0000757 Lack of insight
Expand Tier I Human GO 559 Genes GS208092: GO:0005768 endosome
Expand Tier I Human 39 Genes GS174455: HP:0004347 Weakness of muscles of respiration
Expand Tier I Human 106 Genes GS173246: HP:0001332 Dystonia
Expand Tier I Human GO 7717 Genes GS207616: GO:0016020 membrane
Expand Tier I Human GO 1228 Genes GS199113: GO:0015031 protein transport
Expand Tier I Human 43 Genes GS171083: HP:0001328 Specific learning disability
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human GO 4201 Genes GS195112: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human 542 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human GO 1266 Genes GS197769: GO:0045184 establishment of protein localization
Expand Tier I Human 53 Genes GS173243: HP:0001336 Myoclonus
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 3 Genes GS175955: HP:0002442 Dyscalculia
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human GO 1925 Genes GS201025: GO:0071702 organic substance transport
Expand Tier I Human 40 Genes GS175194: HP:0002063 Rigidity
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
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 Human 27 Genes GS175851: HP:0000733 Stereotypic behavior
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human 3 Genes GS173208: HP:0002446 Astrocytosis
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 123 Genes GS176799: HP:0001265 Hyporeflexia
Expand Tier I Human 90 Genes GS171351: HP:0003581 Adult onset
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 95 Genes GS174135: HP:0002015 Dysphagia
Expand Tier I Human 160 Genes GS176803: HP:0001260 Dysarthria
Expand Tier I Human GO 3310 Genes GS209452: GO:0006810 transport
Expand Tier I Human GO 1515 Genes GS194138: GO:0005739 mitochondrion
Expand Tier I Human 908 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Human 273 Genes GS172516: HP:0001347 Hyperreflexia
Expand Tier I Human GO 1690 Genes GS194905: GO:0008219 cell death
Expand Tier I Human 65 Genes GS170884: HP:0006919 Abnormal aggressive, impulsive or violent behavior
Expand Tier I Human 733 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human 607 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human 7 Genes GS172889: HP:0002371 Loss of speech
Expand Tier I Human GO 320 Genes GS210005: GO:0044440 endosomal part
Expand Tier I Human 25 Genes GS173064: HP:0003678 Rapidly progressive
Expand Tier I Human GO 140 Genes GS195505: GO:0016197 endosomal transport
Expand Tier I Human 1046 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human CTD 5732 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
Expand Tier I Human 15 Genes GS171130: HP:0000751 Personality changes
Expand Tier I Human 203 Genes GS171621: HP:0100851 Abnormal emotion/affect behavior
Expand Tier I Human GO 3364 Genes GS194459: GO:0051234 establishment of localization
Expand Tier I Human 16 Genes GS174301: HP:0000719 Inappropriate behavior
Expand Tier I Human 917 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 604 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human GO 2361 Genes GS195036: GO:0031090 organelle membrane
Expand Tier I Human 42 Genes GS172670: HP:0002363 Abnormality of the brainstem
Expand Tier I Human 985 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Human 15 Genes GS172584: HP:0000741 Apathy
Expand Tier I Human 107 Genes GS176797: HP:0001268 Mental deterioration
Expand Tier I Human 21 Genes GS174553: HP:0002380 Fasciculations
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
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 532 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human GO 1820 Genes GS205820: GO:0033036 macromolecule localization
Expand Tier I Human 62 Genes GS174055: HP:0000726 Dementia
Expand Tier I Human 229 Genes GS175577: HP:0003202 Amyotrophy
Expand Tier I Human 95 Genes GS170930: HP:0001284 Areflexia
Expand Tier I Human GO 10576 Genes GS203594: GO:0043226 organelle
Expand Tier I Human 529 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human 38 Genes GS171132: HP:0000020 Urinary incontinence
Expand Tier I Human 6 Genes GS173047: HP:0002310 Orofacial dyskinesia
Expand Tier I Human GO 6743 Genes GS210002: GO:0044444 cytoplasmic part