Gene Details



KCTD7 and homologs in 1 species are found in 58 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 7808 Genes GS207616: GO:0016020 membrane
Expand Tier I Human 416 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier I Human 616 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human GO 4213 Genes GS195112: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human GO 772 Genes GS196593: GO:0006461 protein complex assembly
Expand Tier I Human GO 6769 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human 26 Genes GS176290: HP:0002123 Generalized myoclonic seizures
Expand Tier I Human 92 Genes GS173061: HP:0003676 Progressive disorder
Expand Tier I Human 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 316 Genes GS170825: HP:0002167 Neurological speech impairment
Expand Tier I Human GO 1160 Genes GS206657: GO:0043933 macromolecular complex subunit organization
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 491 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Human 261 Genes GS176172: HP:0001251 Ataxia
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 1544 Genes GS195733: GO:0022607 cellular component assembly
Expand Tier I Human GO 1699 Genes GS203755: GO:0016265 death
Expand Tier I Human 162 Genes GS175556: HP:0011675 Arrhythmia
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human GO 774 Genes GS208730: GO:0070271 protein complex biogenesis
Expand Tier I Human GO 893 Genes GS203289: GO:0071822 protein complex subunit organization
Expand Tier I Human 50 Genes GS172258: HP:0002197 Generalized seizures
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human GO 226 Genes GS206395: GO:0051260 protein homooligomerization
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 416 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Human GO 4283 Genes GS197009: GO:0005886 plasma membrane
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human 699 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human CTD 102 Genes GS127069: 2,3,7,8-tetrachlorodibenzofuran interacting genes (MeSH:C014211) in CTD
Expand Tier I Human 161 Genes GS176803: HP:0001260 Dysarthria
Expand Tier I Human GO 337 Genes GS202075: GO:0051259 protein oligomerization
Expand Tier I Human GO 1685 Genes GS199112: GO:0044085 cellular component biogenesis
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 14 Genes GS172975: HP:0002078 Truncal ataxia
Expand Tier I Human GO 4371 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human 344 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Human GO 1697 Genes GS194905: GO:0008219 cell death
Expand Tier I Human GO 2368 Genes GS207365: GO:0005829 cytosol
Expand Tier I Human GO 994 Genes GS196927: GO:0065003 macromolecular complex assembly
Expand Tier I Human CTD 363 Genes GS125936: Tunicamycin interacting genes (MeSH:D014415) in CTD
Expand Tier I Human GO 4097 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human 416 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier I Human 185 Genes GS173065: HP:0003679 Pace of progression
Expand Tier I Human 374 Genes GS175815: HP:0011025 Abnormality of cardiovascular system physiology