Gene Details



TTBK2 and homologs in 1 species are found in 91 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 Human GO 1718 Genes GS208734: GO:0016740 transferase activity
Expand Tier I Human GO 1851 Genes GS200446: GO:0017076 purine nucleotide binding
Expand Tier I Human GO 1496 Genes GS201792: GO:0032559 adenyl ribonucleotide binding
Expand Tier I Human GO 3863 Genes GS201367: GO:0019538 protein metabolic process
Expand Tier I Human GO 1821 Genes GS205510: GO:0001883 purine nucleoside binding
Expand Human 1715 Genes GS221148: http://www.broadinstitute.org/gsea/msigdb/cards/SIGNAL_TRANSDUCTION
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Human 1715 Genes GS221397: http://www.broadinstitute.org/gsea/msigdb/cards/SIGNAL_TRANSDUCTION
Expand Tier I Human GO 1692 Genes GS203755: GO:0016265 death
Expand Tier I Human GO 9155 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Human 41 Genes GS219767: http://www.broadinstitute.org/gsea/msigdb/cards/REGULATION_OF_PHOSPHORYLATION
Expand Human 36 Genes GS219833: http://www.broadinstitute.org/gsea/msigdb/cards/REGULATION_OF_PROTEIN_MODIFICATION_PROCESS
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human CTD 916 Genes GS121965: Amiodarone interacting genes (MeSH:D000638) in CTD
Expand Tier I Human GO 15151 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 1832 Genes GS205511: GO:0001882 nucleoside binding
Expand Human 1715 Genes GS222093: http://www.broadinstitute.org/gsea/msigdb/cards/SIGNAL_TRANSDUCTION
Expand Tier I Human GO 5400 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Human GO 2455 Genes GS199032: GO:0036211 protein modification process
Expand Tier I Human 341 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Human GO 1690 Genes GS194905: GO:0008219 cell death
Expand Tier I Human GO 590 Genes GS198285: GO:0004672 protein kinase activity
Expand Tier I Human GO 7259 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human GO 762 Genes GS206251: GO:0016301 kinase activity
Expand Tier I Human GO 128 Genes GS208188: GO:0018209 peptidyl-serine modification
Expand Tier I Human GO 5348 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Human GO 707 Genes GS204918: GO:0016773 phosphotransferase activity, alcohol group as acceptor
Expand Tier I Human 12 Genes GS175406: HP:0002073 Progressive cerebellar ataxia
Expand Tier I Human GO 2549 Genes GS194336: GO:0043412 macromolecule modification
Expand Human 17 Genes GS221128: http://www.broadinstitute.org/gsea/msigdb/cards/POSITIVE_REGULATION_OF_PHOSPHORYLATION
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human CTD 5732 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human 413 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier I Human GO 2411 Genes GS203886: GO:1901265 nucleoside phosphate binding
Expand Tier I Human GO 5764 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human 471 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Human 917 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human GO 116 Genes GS193871: GO:0018105 peptidyl-serine phosphorylation
Expand Tier I Human GO 1466 Genes GS205179: GO:0005524 ATP binding
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human GO 8645 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human GO 1257 Genes GS197087: GO:0016310 phosphorylation
Expand Tier I Human 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 1822 Genes GS197443: GO:0032549 ribonucleoside binding
Expand Tier I Human GO 636 Genes GS199538: GO:0018193 peptidyl-amino acid modification
Expand Tier I Human GO 1109 Genes GS196587: GO:0006468 protein phosphorylation
Expand Tier I Human 397 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Human GO 2423 Genes GS209232: GO:0006796 phosphate-containing compound metabolic process
Expand Tier I Human 87 Genes GS176588: HP:0001272 Cerebellar atrophy
Expand Tier I Human 496 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Human GO 1818 Genes GS201799: GO:0032550 purine ribonucleoside binding
Expand Tier I Human GO 1859 Genes GS201800: GO:0032553 ribonucleotide binding
Expand Tier I Human 695 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier III Human 2216 Genes GS222813: The Druggable Gene Interaction Database
Expand Tier I Human GO 5280 Genes GS209455: GO:0003824 catalytic activity
Expand Human 20 Genes GS219759: http://www.broadinstitute.org/gsea/msigdb/cards/POSITIVE_REGULATION_OF_PROTEIN_MODIFICATION_PROCESS
Expand Tier I Human CTD 908 Genes GS124805: decitabine interacting genes (MeSH:C014347) in CTD
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 425 Genes GS198279: GO:0004674 protein serine/threonine kinase activity
Expand Tier I Human GO 3239 Genes GS200602: GO:0044267 cellular protein metabolic process
Expand Tier I Human GO 1809 Genes GS202716: GO:0035639 purine ribonucleoside triphosphate binding
Expand Tier I Human GO 7308 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human GO 8948 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Human 17 Genes GS219772: http://www.broadinstitute.org/gsea/msigdb/cards/POSITIVE_REGULATION_OF_PHOSPHORYLATION
Expand Tier I Human GO 2455 Genes GS196595: GO:0006464 cellular protein modification process
Expand Tier I Human GO 1500 Genes GS203649: GO:0030554 adenyl nucleotide binding
Expand Tier I Human 413 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Human 21 Genes GS219773: http://www.broadinstitute.org/gsea/msigdb/cards/REGULATION_OF_PROTEIN_AMINO_ACID_PHOSPHORYLATION
Expand Human 17 Genes GS221377: http://www.broadinstitute.org/gsea/msigdb/cards/POSITIVE_REGULATION_OF_PHOSPHORYLATION
Expand Tier I Human GO 2603 Genes GS196343: GO:0036094 small molecule binding
Expand Tier I Human GO 6605 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human GO 1844 Genes GS201794: GO:0032555 purine ribonucleotide binding
Expand Tier I Human GO 885 Genes GS204919: GO:0016772 transferase activity, transferring phosphorus-containing groups
Expand Tier I Human 315 Genes GS170825: HP:0002167 Neurological speech impairment
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Human 19 Genes GS219771: http://www.broadinstitute.org/gsea/msigdb/cards/POSITIVE_REGULATION_OF_PHOSPHATE_METABOLIC_PROCESS
Expand Human 1715 Genes GS219769: http://www.broadinstitute.org/gsea/msigdb/cards/SIGNAL_TRANSDUCTION
Expand Tier I Human 259 Genes GS176172: HP:0001251 Ataxia
Expand Tier III Human 721 Genes GS218676: Differentially expressed in hippocampus of chronic alcoholics.
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human 413 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 160 Genes GS176803: HP:0001260 Dysarthria
Expand Tier I Human GO 2486 Genes GS209235: GO:0006793 phosphorus metabolic process
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 2374 Genes GS206737: GO:0043168 anion binding
Expand Tier I Human GO 2410 Genes GS209108: GO:0000166 nucleotide binding