Gene Details



PNKD and homologs in 1 species are found in 106 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 32 Genes GS172731: HP:0011463 Childhood onset
Expand Tier I Human GO 10576 Genes GS203594: GO:0043226 organelle
Expand Tier I Human CTD 1541 Genes GS125445: Phenobarbital interacting genes (MeSH:D010634) in CTD
Expand Tier I Human GO 1682 Genes GS204629: GO:1901564 organonitrogen compound metabolic process
Expand Tier I Human GO 6743 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human 1203 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human GO 5120 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Tier I Human 37 Genes GS175612: HP:0005346 Abnormal facial expression
Expand Tier I Human 14 Genes GS176209: HP:0000473 Spasmodic torticollis
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 7 Genes GS174033: HP:0005324 Disturbance of facial expression
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human GO 54 Genes GS194084: GO:0042398 cellular modified amino acid biosynthetic process
Expand Tier I Human GO 9526 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 9155 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human GO 20 Genes GS206573: GO:0019184 nonribosomal peptide biosynthetic process
Expand Tier I Human GO 2509 Genes GS207903: GO:0044281 small molecule metabolic process
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
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 95 Genes GS174135: HP:0002015 Dysphagia
Expand Tier I Human 160 Genes GS176803: HP:0001260 Dysarthria
Expand Tier I Human GO 2331 Genes GS208037: GO:0016787 hydrolase activity
Expand Tier I Human CTD 870 Genes GS126764: Calcitriol interacting genes (MeSH:D002117) in CTD
Expand Tier I Human GO 3902 Genes GS198323: GO:0046872 metal ion binding
Expand Tier I Human 33 Genes GS175389: HP:0011006 Abnormality of the musculature of the neck
Expand Tier I Human GO 434 Genes GS202416: GO:0044711 single-organism biosynthetic process
Expand Tier I Human GO 1515 Genes GS194138: GO:0005739 mitochondrion
Expand Tier I Human GO 234 Genes GS209234: GO:0006790 sulfur compound metabolic process
Expand Tier I Human 35 Genes GS176798: HP:0001266 Choreoathetosis
Expand Tier I Human 908 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Human GO 259 Genes GS200383: GO:0046394 carboxylic acid biosynthetic process
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 845 Genes GS204326: GO:0019752 carboxylic acid metabolic process
Expand Tier I Human GO 197 Genes GS204383: GO:0006575 cellular modified amino acid metabolic process
Expand Tier I Human 840 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human 1002 Genes GS174914: HP:0003011 Abnormality of the musculature
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 GO 5928 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human GO 5014 Genes GS210357: GO:0044249 cellular biosynthetic process
Expand Tier I Human 20 Genes GS173094: HP:0004373 Focal dystonia
Expand Tier I Human GO 952 Genes GS202555: GO:0043436 oxoacid metabolic process
Expand Tier I Human GO 1974 Genes GS203688: GO:0008270 zinc ion binding
Expand Tier I Human CTD 159 Genes GS125154: salinomycin interacting genes (MeSH:C010327) in CTD
Expand Tier I Human GO 5908 Genes GS195199: GO:0005634 nucleus
Expand Tier I Human 4 Genes GS176611: HP:0000273 Facial grimacing
Expand Tier I Human CTD 1192 Genes GS125069: Sodium Selenite interacting genes (MeSH:D018038) in CTD
Expand Tier I Human GO 2216 Genes GS209291: GO:0046914 transition metal ion binding
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 1046 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human GO 3697 Genes GS194499: GO:0044271 cellular nitrogen compound biosynthetic process
Expand Tier I Human CTD 4391 Genes GS123768: Cyclosporine interacting genes (MeSH:D016572) in CTD
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 5764 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human GO 50 Genes GS200161: GO:0043604 amide biosynthetic process
Expand Tier I Human GO 91 Genes GS195023: GO:0006518 peptide metabolic process
Expand Tier I Human GO 646 Genes GS204631: GO:1901566 organonitrogen compound biosynthetic process
Expand Tier I Human GO 49 Genes GS196156: GO:0006749 glutathione metabolic process
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 731 Genes GS208043: GO:0016788 hydrolase activity, acting on ester bonds
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human 2 Genes GS176499: HP:0007098 Paroxysmal choreoathetosis
Expand Tier I Human GO 104 Genes GS195577: GO:0016790 thiolester hydrolase activity
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 259 Genes GS195145: GO:0016053 organic acid biosynthetic process
Expand Tier I Human CTD 6287 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human GO 29 Genes GS208490: GO:0043043 peptide biosynthetic process
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 53 Genes GS175407: HP:0002072 Chorea
Expand Tier I Human GO 113 Genes GS204687: GO:0044272 sulfur compound biosynthetic process
Expand Tier I Human GO 4003 Genes GS208978: GO:0043169 cation binding
Expand Tier I Human 218 Genes GS175994: HP:0000464 Abnormality of the neck
Expand Tier I Human GO 19 Genes GS208635: GO:0006750 glutathione biosynthetic process
Expand Tier I Human 695 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human GO 970 Genes GS210163: GO:0006082 organic acid metabolic process
Expand Tier I Human GO 5190 Genes GS207857: GO:0009058 biosynthetic 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 521 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Human 4 Genes GS171945: HP:0002268 Paroxysmal dystonia
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 106 Genes GS173246: HP:0001332 Dystonia
Expand Tier I Human GO 8948 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human GO 7717 Genes GS207616: GO:0016020 membrane
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human 8 Genes GS173144: HP:0002411 Myokymia
Expand Tier I Human CTD 5081 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Tier I Human GO 140 Genes GS200166: GO:0043603 cellular amide metabolic process
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 542 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human GO 422 Genes GS207919: GO:0044283 small molecule biosynthetic process
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 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 GO 3 Genes GS207250: GO:0004416 hydroxyacylglutathione hydrolase activity
Expand Tier I Human GO 5567 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process