Gene Details



KCNA1 and homologs in 1 species are found in 151 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 785 Genes GS195226: GO:0015075 ion transmembrane transporter activity
Expand Tier I Human 317 Genes GS176591: HP:0001276 Hypertonia
Expand Tier I Human CTD 58 Genes GS125569: olanzapine interacting genes (MeSH:C076029) in CTD
Expand Tier I Human GO 203 Genes GS198194: GO:0034702 ion channel complex
Expand Tier I Human GO 769 Genes GS196593: GO:0006461 protein complex assembly
Expand Tier I Human CTD 62 Genes GS126983: Dopamine interacting genes (MeSH:D004298) in CTD
Expand Tier I Human 34 Genes GS172732: HP:0001751 Vestibular dysfunction
Expand Tier I Human 6 Genes GS172755: HP:0001350 Slurred speech
Expand Tier I Human GO 7609 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human GO 133 Genes GS194234: GO:0033267 axon part
Expand Tier I Human GO 497 Genes GS196432: GO:0030001 metal ion transport
Expand Tier I Human 829 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human CTD 4424 Genes GS123718: Ethinyl Estradiol interacting genes (MeSH:D004997) in CTD
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 384 Genes GS171708: HP:0000359 Abnormality of the inner ear
Expand Tier I Human 97 Genes GS175976: HP:0003621 Juvenile onset
Expand Tier I Human GO 224 Genes GS210290: GO:0016324 apical plasma membrane
Expand Tier I Human GO 1905 Genes GS198782: GO:0044459 plasma membrane part
Expand Tier I Human GO 178 Genes GS205810: GO:0022832 voltage-gated channel activity
Expand Tier I Human GO 1691 Genes GS209960: GO:0003008 system process
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 23 Genes GS173380: HP:0002064 Spastic gait
Expand Tier I Human 1222 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human GO 1541 Genes GS195733: GO:0022607 cellular component assembly
Expand Tier I Human GO 70 Genes GS198193: GO:0034705 potassium channel complex
Expand Tier I Human GO 302 Genes GS205812: GO:0022836 gated channel activity
Expand Tier I Human 83 Genes GS174968: HP:0003236 Elevated serum creatine phosphokinase
Expand Tier I Human GO 318 Genes GS195230: GO:0015077 monovalent inorganic cation transmembrane transporter activity
Expand Tier I Human 576 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 70 Genes GS204008: GO:0008076 voltage-gated potassium channel complex
Expand Tier I Human 214 Genes GS176167: HP:0001257 Spasticity
Expand Tier I Human GO 15151 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human 550 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human GO 5359 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Human GO 335 Genes GS202075: GO:0051259 protein oligomerization
Expand Tier I Human GO 419 Genes GS202908: GO:0022803 passive transmembrane transporter activity
Expand Tier I Human CTD 7 Genes GS125234: Tetraethylammonium interacting genes (MeSH:D019789) in CTD
Expand Tier I Human GO 78 Genes GS201107: GO:0005249 voltage-gated potassium channel activity
Expand Tier I Human GO 5243 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Human GO 3853 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Human GO 401 Genes GS205817: GO:0022838 substrate-specific channel activity
Expand Tier I Human 1002 Genes GS174914: HP:0003011 Abnormality of the musculature
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 825 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human 341 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Human 95 Genes GS171217: HP:0003487 Babinski sign
Expand Tier I Human 107 Genes GS173786: HP:0003457 EMG abnormality
Expand Tier I Human GO 991 Genes GS196927: GO:0065003 macromolecular complex assembly
Expand Tier I Human GO 471 Genes GS198213: GO:0022890 inorganic cation transmembrane transporter activity
Expand Tier I Human GO 4085 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human GO 1254 Genes GS199199: GO:0031226 intrinsic to plasma membrane
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 1098 Genes GS195083: GO:0007267 cell-cell signaling
Expand Tier I Human GO 12 Genes GS196767: GO:0005251 delayed rectifier potassium channel activity
Expand Tier I Human GO 924 Genes GS197610: GO:0022857 transmembrane transporter activity
Expand Tier I Human GO 8 Genes GS209767: GO:0044224 juxtaparanode region of axon
Expand Tier I Human 111 Genes GS177023: HP:0010876 Abnormality of circulating protein level
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human GO 844 Genes GS198212: GO:0022891 substrate-specific transmembrane transporter activity
Expand Tier I Human 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 118 Genes GS209449: GO:0006813 potassium ion transport
Expand Tier I Human 550 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human GO 652 Genes GS195082: GO:0007268 synaptic transmission
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human GO 890 Genes GS203289: GO:0071822 protein complex subunit organization
Expand Tier I Human CTD 287 Genes GS123026: Haloperidol interacting genes (MeSH:D006220) in CTD
Expand Tier I Human GO 132 Genes GS198195: GO:0034703 cation channel complex
Expand Tier I Human GO 225 Genes GS206395: GO:0051260 protein homooligomerization
Expand Tier I Human 170 Genes GS173476: HP:0002311 Incoordination
Expand Tier I Human 212 Genes GS176185: HP:0100790 Hernia
Expand Tier I Human 49 Genes GS173398: HP:0000776 Congenital diaphragmatic hernia
Expand Tier I Human 737 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human GO 393 Genes GS196169: GO:0005216 ion channel activity
Expand Tier I Human GO 4250 Genes GS197009: GO:0005886 plasma membrane
Expand Tier I Human 496 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Human GO 569 Genes GS209735: GO:0008324 cation transmembrane transporter activity
Expand Tier I Human GO 302 Genes GS205816: GO:0022839 ion gated channel activity
Expand Tier I Human 695 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human GO 1223 Genes GS208482: GO:0042995 cell projection
Expand Tier I Human GO 1235 Genes GS202899: GO:0050877 neurological system process
Expand Tier I Human GO 1682 Genes GS199112: GO:0044085 cellular component biogenesis
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 1210 Genes GS197008: GO:0005887 integral to plasma membrane
Expand Tier I Human GO 4575 Genes GS204007: GO:0044700 single organism signaling
Expand Tier I Human GO 110 Genes GS201989: GO:0005267 potassium channel activity
Expand Tier I Human GO 964 Genes GS209451: GO:0006811 ion transport
Expand Tier I Human GO 294 Genes GS209721: GO:0045177 apical part of cell
Expand Tier I Human GO 632 Genes GS209450: GO:0006812 cation transport
Expand Tier I Human GO 7717 Genes GS207616: GO:0016020 membrane
Expand Tier I Human 776 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human 780 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 60 Genes GS173119: HP:0002315 Headache
Expand Tier I Human 413 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier I Human 614 Genes GS176171: HP:0001250 Seizures
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 GO 42 Genes GS195063: GO:0044304 main axon
Expand Tier I Human GO 4201 Genes GS195112: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human 542 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human GO 286 Genes GS202125: GO:0030424 axon
Expand Tier I Human GO 1193 Genes GS196168: GO:0005215 transporter activity
Expand Tier I Human 315 Genes GS170825: HP:0002167 Neurological speech impairment
Expand Tier I Human GO 3271 Genes GS199267: GO:0043234 protein complex
Expand Tier I Human GO 273 Genes GS199357: GO:0005261 cation channel activity
Expand Tier I Human GO 1157 Genes GS206657: GO:0043933 macromolecular complex subunit organization
Expand Tier I Human GO 278 Genes GS195770: GO:0015672 monovalent inorganic cation transport
Expand Tier I Human 60 Genes GS174720: HP:0000775 Abnormality of the diaphragm
Expand Tier I Human 381 Genes GS175714: HP:0011389 Functional abnormality of the inner ear
Expand Tier I Human 259 Genes GS176172: HP:0001251 Ataxia
Expand Tier I Human GO 125 Genes GS210233: GO:0015079 potassium ion transmembrane transporter activity
Expand Tier I Human GO 419 Genes GS195569: GO:0015267 channel activity
Expand Tier I Human GO 374 Genes GS198322: GO:0046873 metal ion transmembrane transporter activity
Expand Tier I Human GO 649 Genes GS207805: GO:0043005 neuron projection
Expand Tier I Human 22 Genes GS174815: HP:0002321 Vertigo
Expand Tier I Human GO 4575 Genes GS206355: GO:0023052 signaling
Expand Tier I Human 413 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human CTD 335 Genes GS122653: Clozapine interacting genes (MeSH:D003024) in CTD
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 3310 Genes GS209452: GO:0006810 transport
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 837 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 908 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Human GO 636 Genes GS201839: GO:0044463 cell projection part
Expand Tier I Human 273 Genes GS172516: HP:0001347 Hyperreflexia
Expand Tier I Human GO 4338 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Human CTD 97 Genes GS124547: Amphetamine interacting genes (MeSH:D000661) in CTD
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 133 Genes GS200620: GO:0022843 voltage-gated cation channel activity
Expand Tier I Human 4 Genes GS176057: HP:0002131 Episodic ataxia
Expand Tier I Human GO 978 Genes GS198214: GO:0022892 substrate-specific transporter activity
Expand Tier I Human 1046 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human CTD 4391 Genes GS123768: Cyclosporine interacting genes (MeSH:D016572) in CTD
Expand Tier I Human 413 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier I Human 83 Genes GS175811: HP:0011021 Abnormality of circulating enzyme level
Expand Tier I Human GO 3364 Genes GS194459: GO:0051234 establishment of localization
Expand Tier I Human 917 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 122 Genes GS173242: HP:0001337 Tremor
Expand Tier I Human GO 178 Genes GS201111: GO:0005244 voltage-gated ion channel activity
Expand Tier I Human GO 771 Genes GS208730: GO:0070271 protein complex biogenesis
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 6073 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component