Gene Details



COLQ and homologs in 1 species are found in 162 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 Human 1003 Genes GS219936: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_PLASMA_MEMBRANE
Expand Tier I Human 112 Genes GS174327: HP:0003198 Myopathy
Expand Tier I Human GO 2112 Genes GS210214: GO:0005576 extracellular region
Expand Human 1375 Genes GS219728: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_MEMBRANE
Expand Human 1375 Genes GS219978: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_MEMBRANE
Expand Tier I Human 529 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human GO 3 Genes GS207510: GO:0001507 acetylcholine catabolic process in synaptic cleft
Expand Human 1733 Genes GS219955: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE_PART
Expand Human 1003 Genes GS219719: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_PLASMA_MEMBRANE
Expand Tier I Human GO 7609 Genes GS201949: GO:0044699 single-organism process
Expand Human 1003 Genes GS221018: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_PLASMA_MEMBRANE
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 829 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Human 1003 Genes GS221267: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_PLASMA_MEMBRANE
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 676 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human GO 370 Genes GS197471: GO:0044456 synapse part
Expand Tier I Human GO 1691 Genes GS209960: GO:0003008 system process
Expand Tier I Human 541 Genes GS174385: HP:0002088 Abnormality of the lung
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human GO 752 Genes GS202715: GO:0035637 multicellular organismal signaling
Expand Tier I Human 535 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Human 1393 Genes GS219979: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_MEMBRANE
Expand Human 1197 Genes GS219982: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE_PART
Expand Tier I Human GO 733 Genes GS196511: GO:0030054 cell junction
Expand Tier I Human GO 9155 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human 10 Genes GS173673: HP:0100295 Muscle fiber atrophy
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 10 Genes GS175458: HP:0003554 Type 2 muscle fiber atrophy
Expand Tier I Human GO 361 Genes GS210217: GO:0005578 proteinaceous extracellular matrix
Expand Tier I Human GO 186 Genes GS201254: GO:0044420 extracellular matrix part
Expand Human 1470 Genes GS219947: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Tier I Human 182 Genes GS174612: HP:0001600 Abnormality of the larynx
Expand Tier I Human GO 23 Genes GS207578: GO:0007271 synaptic transmission, cholinergic
Expand Human 1197 Genes GS219942: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE_PART
Expand Tier I Human 12 Genes GS174326: HP:0003199 Decreased muscle mass
Expand Tier I Human GO 90 Genes GS208328: GO:0005604 basement membrane
Expand Tier I Human 840 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human 15 Genes GS174533: HP:0003388 Easy fatigability
Expand Tier I Human 1002 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human GO 6 Genes GS196213: GO:0008291 acetylcholine metabolic process
Expand Tier III Human 3028 Genes GS137407: Supplementary Table 2. Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier I Human GO 8 Genes GS209040: GO:0043083 synaptic cleft
Expand Tier I Human 825 Genes GS175525: HP:0000004 Onset and clinical course
Expand Human 1733 Genes GS219981: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE_PART
Expand Tier I Human 395 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Human 36 Genes GS173618: HP:0002747 Respiratory insufficiency due to muscle weakness
Expand Tier I Human 255 Genes GS176610: HP:0003593 Infantile onset
Expand Tier I Human 107 Genes GS173786: HP:0003457 EMG abnormality
Expand Human 1197 Genes GS219725: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE_PART
Expand Tier I Human 375 Genes GS176038: HP:0002795 Functional respiratory abnormality
Expand Tier I Human GO 2499 Genes GS196934: GO:0065008 regulation of biological quality
Expand Human 2063 Genes GS219980: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human GO 131 Genes GS207420: GO:0008201 heparin binding
Expand Tier I Human 136 Genes GS171855: HP:0000597 Ophthalmoparesis
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
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 GO 5764 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human GO 1098 Genes GS195083: GO:0007267 cell-cell signaling
Expand Tier I Human 14 Genes GS175354: HP:0003473 Fatigable weakness
Expand Tier I Human 471 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Human GO 173 Genes GS209592: GO:0005539 glycosaminoglycan binding
Expand Human 1197 Genes GS219976: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE_PART
Expand Tier I Human 357 Genes GS172701: HP:0002650 Scoliosis
Expand Human 271 Genes GS220981: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_CYTOKINE_CYTOKINE_RECEPTOR_INTERACTION
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 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human 396 Genes GS171100: HP:0000759 Abnormality of the peripheral nervous system
Expand Human 1733 Genes GS219987: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE_PART
Expand Tier I Human 48 Genes GS172577: HP:0003690 Limb muscle weakness
Expand Tier I Human GO 652 Genes GS195082: GO:0007268 synaptic transmission
Expand Human 1016 Genes GS219722: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_PLASMA_MEMBRANE
Expand Tier I Human GO 6 Genes GS207645: GO:1900619 acetate ester metabolic process
Expand Tier I Human GO 1669 Genes GS202188: GO:0044248 cellular catabolic process
Expand Tier I Human GO 10 Genes GS205551: GO:0042135 neurotransmitter catabolic process
Expand Tier I Human 16 Genes GS174400: HP:0001612 Weak cry
Expand Human 1470 Genes GS219983: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Tier I Human GO 1853 Genes GS209010: GO:1901575 organic substance catabolic process
Expand Tier I Human GO 1555 Genes GS201869: GO:0008104 protein localization
Expand Human 1393 Genes GS219985: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_MEMBRANE
Expand Tier I Human 7 Genes GS177009: HP:0003403 EMG: decremental response of compound muscle action potential (CMAP) to repetitive nerve stimulation
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 222 Genes GS173995: HP:0000508 Ptosis
Expand Tier I Human 737 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human GO 21 Genes GS208327: GO:0005605 basal lamina
Expand Human 271 Genes GS221230: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_CYTOKINE_CYTOKINE_RECEPTOR_INTERACTION
Expand Tier I Human 344 Genes GS172989: HP:0001324 Muscle weakness
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 89 Genes GS198230: GO:0005581 collagen
Expand Tier I Human GO 1235 Genes GS202899: GO:0050877 neurological system process
Expand Human 2063 Genes GS219986: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
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 4575 Genes GS204007: GO:0044700 single organism signaling
Expand Tier I Human 256 Genes GS175602: HP:0002087 Abnormality of the upper respiratory tract
Expand Tier I Human GO 851 Genes GS203972: GO:0005615 extracellular space
Expand Tier I Human GO 1820 Genes GS205820: GO:0033036 macromolecule localization
Expand Tier I Human 33 Genes GS171944: HP:0003324 Generalized muscle weakness
Expand Tier I Human 263 Genes GS175823: HP:0002093 Respiratory insufficiency
Expand Tier I Human 96 Genes GS172854: HP:0004302 Functional motor problems.
Expand Tier I Human GO 8578 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human 58 Genes GS172853: HP:0004303 Abnormality of muscle fibers
Expand Tier I Human GO 7308 Genes GS201431: GO:0005515 protein binding
Expand Human 1393 Genes GS219731: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_MEMBRANE
Expand Tier I Human 39 Genes GS174455: HP:0004347 Weakness of muscles of respiration
Expand Tier I Human GO 8948 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Human 2063 Genes GS219964: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human GO 138 Genes GS201740: GO:0001505 regulation of neurotransmitter levels
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Human 1003 Genes GS219975: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_PLASMA_MEMBRANE
Expand Tier I Human CTD 292 Genes GS124722: kojic acid interacting genes (MeSH:C011890) in CTD
Expand Tier I Human 472 Genes GS171893: HP:0011458 Abdominal symptom
Expand Tier I Human GO 425 Genes GS196302: GO:0031012 extracellular matrix
Expand Tier I Human 532 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Human 2063 Genes GS219747: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human 315 Genes GS170825: HP:0002167 Neurological speech impairment
Expand Human 1470 Genes GS219730: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Tier I Human 189 Genes GS174579: HP:0002031 Abnormality of the esophagus
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Human 1470 Genes GS219977: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Human 271 Genes GS220158: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_CYTOKINE_CYTOKINE_RECEPTOR_INTERACTION
Expand Tier I Human 5 Genes GS173852: HP:0003436 Prolonged miniature endplate currents
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 1094 Genes GS201255: GO:0044421 extracellular region part
Expand Human 1733 Genes GS219738: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE_PART
Expand Tier I Human GO 4575 Genes GS206355: GO:0023052 signaling
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human 7 Genes GS171703: HP:0003443 Decreased size of nerve terminals
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 3 Genes GS200023: GO:0006581 acetylcholine catabolic process
Expand Human 1016 Genes GS219939: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_PLASMA_MEMBRANE
Expand Tier I Human 525 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human GO 4701 Genes GS195977: GO:0007154 cell communication
Expand Tier I Human GO 736 Genes GS204608: GO:0019226 transmission of nerve impulse
Expand Tier I Human 132 Genes GS174606: HP:0001608 Abnormality of the voice
Expand Tier I Human GO 2374 Genes GS206737: GO:0043168 anion binding
Expand Tier I Human CTD 324 Genes GS121837: bexarotene interacting genes (MeSH:C095105) in CTD
Expand Tier I Human GO 1994 Genes GS207862: GO:0009056 catabolic process
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 Human GO 188 Genes GS201611: GO:0097367 carbohydrate derivative binding
Expand Human 1375 Genes GS219945: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_MEMBRANE
Expand Tier I Human 236 Genes GS174292: HP:0011968 Feeding difficulties
Expand Tier I Human 14 Genes GS174744: HP:0003398 Abnormality of the neuromuscular junction
Expand Human 1375 Genes GS219984: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_MEMBRANE
Expand Tier I Human CTD 481 Genes GS122634: Ketone Bodies interacting genes (MeSH:D007657) in CTD
Expand Tier I Human 198 Genes GS171637: HP:0008872 Feeding difficulties in infancy
Expand Tier I Human GO 488 Genes GS205674: GO:0045202 synapse
Expand Tier I Human 1046 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human GO 17 Genes GS201868: GO:0008105 asymmetric protein localization
Expand Human 1393 Genes GS219948: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_MEMBRANE
Expand Tier I Human GO 27 Genes GS205549: GO:0042133 neurotransmitter metabolic process
Expand Human 271 Genes GS219636: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_CYTOKINE_CYTOKINE_RECEPTOR_INTERACTION
Expand Tier I Human 77 Genes GS172684: HP:0003307 Hyperlordosis