Gene Details



WNK4 and homologs in 1 species are found in 129 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 10 Genes GS207794: GO:0030157 pancreatic juice secretion
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 348 Genes GS197668: GO:0051241 negative regulation of multicellular organismal process
Expand Tier I Human GO 3863 Genes GS201367: GO:0019538 protein metabolic process
Expand Tier I Human GO 7609 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human GO 1821 Genes GS205510: GO:0001883 purine nucleoside binding
Expand Tier I Human GO 5623 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human GO 1691 Genes GS209960: GO:0003008 system process
Expand Tier I Human GO 270 Genes GS207070: GO:0051051 negative regulation of transport
Expand Tier I Human 1222 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
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 GO 8094 Genes GS202316: GO:0050789 regulation of biological process
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 1832 Genes GS205511: GO:0001882 nucleoside binding
Expand Tier I Human GO 5400 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Human GO 28 Genes GS196356: GO:0006821 chloride transport
Expand Tier I Human GO 2455 Genes GS199032: GO:0036211 protein modification process
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human GO 846 Genes GS203276: GO:0007243 intracellular protein kinase cascade
Expand Tier I Human 4 Genes GS175776: HP:0008242 Pseudohypoaldosteronism
Expand Tier I Human GO 288 Genes GS209188: GO:0005911 cell-cell junction
Expand Tier I Human GO 590 Genes GS198285: GO:0004672 protein kinase activity
Expand Tier I Human 10 Genes GS172436: HP:0002153 Hyperkalemia
Expand Tier I Human GO 456 Genes GS204054: GO:0044057 regulation of system process
Expand Tier I Human GO 762 Genes GS206251: GO:0016301 kinase activity
Expand Tier I Human GO 5348 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Human 167 Genes GS171201: HP:0001941 Acidosis
Expand Tier I Human GO 2499 Genes GS196934: GO:0065008 regulation of biological quality
Expand Tier I Human GO 55 Genes GS209827: GO:0015698 inorganic anion transport
Expand Tier I Human 86 Genes GS172544: HP:0000834 Abnormality of the adrenal glands
Expand Tier I Human GO 2549 Genes GS194336: GO:0043412 macromolecule modification
Expand Tier I Human CTD 363 Genes GS125936: Tunicamycin interacting genes (MeSH:D014415) in CTD
Expand Tier I Human GO 3 Genes GS207369: GO:0090186 regulation of pancreatic juice secretion
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 GO 4134 Genes GS200341: GO:0051179 localization
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 372 Genes GS175815: HP:0011025 Abnormality of cardiovascular system physiology
Expand Tier I Human GO 97 Genes GS196134: GO:0005923 tight junction
Expand Tier I Human GO 3364 Genes GS194459: GO:0051234 establishment of localization
Expand Tier I Human GO 595 Genes GS202897: GO:0050878 regulation of body fluid levels
Expand Tier I Human GO 791 Genes GS196790: GO:0046903 secretion
Expand Tier I Human GO 113 Genes GS206185: GO:0043296 apical junction complex
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 1323 Genes GS207293: GO:0032879 regulation of localization
Expand Tier I Human GO 8 Genes GS196437: GO:0060457 negative regulation of digestive system process
Expand Tier I Human GO 1257 Genes GS197087: GO:0016310 phosphorylation
Expand Tier I Human GO 438 Genes GS202796: GO:0051046 regulation of secretion
Expand Tier I Human 13 Genes GS173708: HP:0000847 Abnormality of renin-angiotensin system
Expand Tier I Human GO 1822 Genes GS197443: GO:0032549 ribonucleoside binding
Expand Tier I Human 38 Genes GS170846: HP:0010930 Abnormality of monovalent inorganic cation homeostasis
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human GO 20 Genes GS204564: GO:0044058 regulation of digestive system process
Expand Tier I Human GO 313 Genes GS196355: GO:0006820 anion transport
Expand Tier I Human GO 1109 Genes GS196587: GO:0006468 protein phosphorylation
Expand Tier I Human CTD 595 Genes GS121595: Dexamethasone interacting genes (MeSH:D003907) in CTD
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 3 Genes GS207367: GO:0090188 negative regulation of pancreatic juice secretion
Expand Tier I Human GO 1555 Genes GS201869: GO:0008104 protein localization
Expand Tier I Human GO 2423 Genes GS209232: GO:0006796 phosphate-containing compound metabolic process
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 6 Genes GS173849: HP:0003351 Decreased circulating renin level
Expand Tier I Human 29 Genes GS174566: HP:0011042 Abnormality of potassium homeostasis
Expand Tier I Human CTD 768 Genes GS123769: 2-(1'H-indolo-3'-carbonyl)thiazole-4-carboxylic acid methyl ester interacting genes (MeSH:C548651) in CTD
Expand Tier I Human 141 Genes GS172281: HP:0000822 Hypertension
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
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 115 Genes GS172364: HP:0003111 Abnormality of ion homeostasis
Expand Tier I Human GO 113 Genes GS197389: GO:0007586 digestion
Expand Tier III Human 2216 Genes GS222813: The Druggable Gene Interaction Database
Expand Tier I Human 50 Genes GS171198: HP:0001942 Metabolic acidosis
Expand Tier I Human 511 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human GO 1766 Genes GS194455: GO:0051239 regulation of multicellular organismal process
Expand Tier I Human GO 7650 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier I Human GO 5280 Genes GS209455: GO:0003824 catalytic activity
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 4575 Genes GS204007: GO:0044700 single organism signaling
Expand Tier I Human GO 3239 Genes GS200602: GO:0044267 cellular protein metabolic process
Expand Tier I Human GO 1820 Genes GS205820: GO:0033036 macromolecule localization
Expand Tier I Human GO 964 Genes GS209451: GO:0006811 ion transport
Expand Tier I Human 182 Genes GS173028: HP:0004360 Abnormality of acid-base homeostasis
Expand Tier I Human GO 1809 Genes GS202716: GO:0035639 purine ribonucleoside triphosphate binding
Expand Tier I Human GO 8578 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human GO 123 Genes GS202798: GO:0051048 negative regulation of secretion
Expand Tier I Human GO 73 Genes GS197388: GO:0007589 body fluid secretion
Expand Tier I Human GO 8948 Genes GS201023: GO:0071704 organic substance metabolic process
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 101 Genes GS176735: HP:0010929 Abnormality of cation homeostasis
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human CTD 5081 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Tier I Human GO 4960 Genes GS199124: GO:0051716 cellular response to stimulus
Expand Tier I Human GO 54 Genes GS195734: GO:0022600 digestive system process
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 886 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human GO 3098 Genes GS203058: GO:0048519 negative regulation of biological process
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human 61 Genes GS175742: HP:0011733 Abnormality of adrenal physiology
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 4575 Genes GS206355: GO:0023052 signaling
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 4065 Genes GS209199: GO:0007165 signal transduction
Expand Tier I Human GO 963 Genes GS202799: GO:0051049 regulation of transport
Expand Tier I Human GO 3310 Genes GS209452: GO:0006810 transport
Expand Tier I Human GO 2486 Genes GS209235: GO:0006793 phosphorus metabolic process
Expand Tier I Human GO 4701 Genes GS195977: GO:0007154 cell communication
Expand Tier I Human 908 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Human GO 2374 Genes GS206737: GO:0043168 anion binding
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 2410 Genes GS209108: GO:0000166 nucleotide binding
Expand Tier I Human GO 7259 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human GO 1810 Genes GS198274: GO:0035556 intracellular signal transduction
Expand Tier I Human GO 97 Genes GS200067: GO:0070160 occluding junction
Expand Tier I Human GO 6548 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human GO 707 Genes GS204918: GO:0016773 phosphotransferase activity, alcohol group as acceptor