Gene Details



SCN9A and homologs in 1 species are found in 210 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 CTD 306 Genes GS126769: Calcium interacting genes (MeSH:D002118) in CTD
Expand Tier I Human GO 203 Genes GS198194: GO:0034702 ion channel complex
Expand Tier I Human GO 1191 Genes GS207015: GO:0042592 homeostatic process
Expand Tier I Human 14 Genes GS171481: HP:0003552 Muscle stiffness
Expand Tier I Human GO 14 Genes GS206110: GO:0001518 voltage-gated sodium channel complex
Expand Tier I Human 882 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human GO 333 Genes GS204027: GO:0044708 single-organism behavior
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 8 Genes GS174784: HP:0002045 Hypothermia
Expand Tier I Human GO 497 Genes GS196432: GO:0030001 metal ion transport
Expand Tier I Human 32 Genes GS172172: HP:0002270 Abnormality of the autonomic nervous system
Expand Tier I Human 832 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human GO 484 Genes GS197644: GO:0006954 inflammatory response
Expand Tier I Human 12 Genes GS171599: HP:0001962 Palpitations
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human CTD 1 Genes GS121685: brevetoxin 3 interacting genes (MeSH:C546612) in CTD
Expand Tier I Human 414 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human 680 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human 97 Genes GS175976: HP:0003621 Juvenile onset
Expand Tier I Human CTD 62 Genes GS124975: Lithium Chloride interacting genes (MeSH:D018021) in CTD
Expand Tier I Human GO 1914 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 1693 Genes GS209960: GO:0003008 system process
Expand Tier I Human 545 Genes GS174385: HP:0002088 Abnormality of the lung
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human GO 751 Genes GS202715: GO:0035637 multicellular organismal signaling
Expand Tier I Human 1228 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human 104 Genes GS171247: HP:0002019 Constipation
Expand Tier I Human CTD 3171 Genes GS127127: Benzo(a)pyrene interacting genes (MeSH:D001564) in CTD
Expand Tier I Human 4 Genes GS172929: HP:0004409 Hyposmia
Expand Tier I Human GO 10 Genes GS204898: GO:0031420 alkali metal ion binding
Expand Tier I Human GO 302 Genes GS205812: GO:0022836 gated channel activity
Expand Tier I Human 14 Genes GS176634: HP:0000458 Anosmia
Expand Tier I Human 174 Genes GS172015: HP:0000969 Edema
Expand Tier I Human GO 12 Genes GS200721: GO:0048266 behavioral response to pain
Expand Tier I Human GO 318 Genes GS195230: GO:0015077 monovalent inorganic cation transmembrane transporter activity
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 5436 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Human GO 2940 Genes GS210507: GO:0006950 response to stress
Expand Tier I Human GO 419 Genes GS202908: GO:0022803 passive transmembrane transporter activity
Expand Tier I Human GO 248 Genes GS194078: GO:0042391 regulation of membrane potential
Expand Tier I Human 129 Genes GS173090: HP:0004377 Hematological neoplasm
Expand Tier I Human GO 5320 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Human 10 Genes GS177026: HP:0000217 Xerostomia
Expand Tier I Human CTD 13 Genes GS126537: Catecholamines interacting genes (MeSH:D002395) in CTD
Expand Tier I Human GO 3861 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Human GO 401 Genes GS205817: GO:0022838 substrate-specific channel activity
Expand Tier I Human 1006 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human 266 Genes GS171645: HP:0011843 Abnormality of skeletal physiology
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human GO 1106 Genes GS204150: GO:0009611 response to wounding
Expand Tier I Human 255 Genes GS176610: HP:0003593 Infantile onset
Expand Tier I Human GO 649 Genes GS198498: GO:0050801 ion homeostasis
Expand Tier I Human 1 Genes GS174616: HP:0200025 Mandibular pain
Expand Tier I Human 111 Genes GS175068: HP:0000971 Abnormality of the sweat gland
Expand Tier I Human 285 Genes GS175119: HP:0001881 Abnormality of leukocytes
Expand Tier I Human GO 2507 Genes GS196934: GO:0065008 regulation of biological quality
Expand Tier I Human GO 471 Genes GS198213: GO:0022890 inorganic cation transmembrane transporter activity
Expand Tier I Human GO 1262 Genes GS199199: GO:0031226 intrinsic to plasma membrane
Expand Tier I Human 246 Genes GS176806: HP:0003812 Phenotypic variability
Expand Tier I Human GO 88 Genes GS201124: GO:0009791 post-embryonic development
Expand Tier I Human GO 507 Genes GS206091: GO:0007610 behavior
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 715 Genes GS200565: GO:0019725 cellular homeostasis
Expand Tier I Human GO 4144 Genes GS200341: GO:0051179 localization
Expand Tier I Human GO 5810 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human 374 Genes GS175815: HP:0011025 Abnormality of cardiovascular system physiology
Expand Tier I Human GO 925 Genes GS197610: GO:0022857 transmembrane transporter activity
Expand Tier I Human GO 4070 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human 148 Genes GS173537: HP:0001872 Abnormality of thrombocytes
Expand Tier I Human CTD 120 Genes GS126673: Fish Oils interacting genes (MeSH:D005395) in CTD
Expand Tier I Human 285 Genes GS171902: HP:0010987 Abnormality of cellular immune system
Expand Tier I Human 941 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human GO 845 Genes GS198212: GO:0022891 substrate-specific transmembrane transporter activity
Expand Tier I Human 399 Genes GS171100: HP:0000759 Abnormality of the peripheral nervous system
Expand Tier I Human CTD 527 Genes GS125792: Ethanol interacting genes (MeSH:D000431) in CTD
Expand Tier I Human GO 2741 Genes GS195668: GO:0042221 response to chemical stimulus
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human GO 24 Genes GS201274: GO:0048265 response to pain
Expand Tier I Human 364 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human 786 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human GO 132 Genes GS198195: GO:0034703 cation channel complex
Expand Tier I Human 639 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human GO 1100 Genes GS206909: GO:0006952 defense response
Expand Tier I Human 31 Genes GS175341: HP:0100755 Abnormality of salivation
Expand Tier I Human GO 4283 Genes GS197009: GO:0005886 plasma membrane
Expand Tier I Human GO 569 Genes GS209735: GO:0008324 cation transmembrane transporter activity
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 8 Genes GS176646: HP:0010819 Atonic seizures
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human GO 302 Genes GS205816: GO:0022839 ion gated channel activity
Expand Tier I Human 403 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Human 44 Genes GS174484: HP:0000521 Abnormality of tear glands or tear production
Expand Tier I Human GO 5 Genes GS200966: GO:0031402 sodium ion binding
Expand Tier I Human GO 110 Genes GS203103: GO:0006814 sodium ion transport
Expand Tier I Human 17 Genes GS173375: HP:0010832 Abnormality of pain sensation
Expand Tier I Human GO 837 Genes GS196920: GO:0048878 chemical homeostasis
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 1218 Genes GS197008: GO:0005887 integral to plasma membrane
Expand Tier I Human GO 4593 Genes GS204007: GO:0044700 single organism signaling
Expand Tier I Human GO 8622 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human 22 Genes GS173263: HP:0003623 Neonatal onset
Expand Tier I Human CTD 62 Genes GS121654: Sodium interacting genes (MeSH:D012964) in CTD
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 14 Genes GS174165: HP:0001662 Bradycardia
Expand Tier I Human GO 632 Genes GS209450: GO:0006812 cation transport
Expand Tier I Human 588 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human GO 7808 Genes GS207616: GO:0016020 membrane
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 102 Genes GS172692: HP:0002659 Increased susceptibility to fractures
Expand Tier I Human 473 Genes GS171893: HP:0011458 Abdominal symptom
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 49 Genes GS175085: HP:0000989 Pruritus
Expand Tier I Human 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human GO 1195 Genes GS196168: GO:0005215 transporter activity
Expand Tier I Human 98 Genes GS171910: HP:0003828 Variable expressivity
Expand Tier I Human 739 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human GO 3275 Genes GS199267: GO:0043234 protein complex
Expand Tier I Human GO 273 Genes GS199357: GO:0005261 cation channel activity
Expand Tier I Human GO 278 Genes GS195770: GO:0015672 monovalent inorganic cation transport
Expand Tier I Human 4 Genes GS172649: HP:0007021 Pain insensitivity
Expand Tier I Human 626 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Human GO 136 Genes GS201741: GO:0001508 regulation of action potential
Expand Tier I Human 360 Genes GS174099: HP:0011793 Neoplasm by anatomical site
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 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human 50 Genes GS172258: HP:0002197 Generalized seizures
Expand Tier I Human 213 Genes GS176040: HP:0011032 Abnormality of fluid regulation
Expand Tier I Human 11 Genes GS172911: HP:0002373 Febrile seizures
Expand Tier I Human 39 Genes GS173693: HP:0001649 Tachycardia
Expand Tier I Human GO 4593 Genes GS206355: GO:0023052 signaling
Expand Tier I Human GO 586 Genes GS201310: GO:0006873 cellular ion homeostasis
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 90 Genes GS172611: HP:0003474 Sensory impairment
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human 28 Genes GS172919: HP:0004408 Abnormality of the sense of smell
Expand Tier I Human 275 Genes GS174338: HP:0002719 Recurrent infections
Expand Tier I Human 177 Genes GS175431: HP:0011122 Abnormality of skin physiology
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 98 Genes GS204614: GO:0019228 regulation of action potential in neuron
Expand Tier I Human 207 Genes GS176283: HP:0009830 Peripheral neuropathy
Expand Tier I Human GO 3934 Genes GS198323: GO:0046872 metal ion binding
Expand Tier I Human GO 123 Genes GS208052: GO:0015081 sodium ion transmembrane transporter activity
Expand Tier I Human 4 Genes GS171418: HP:0002661 Painless fractures due to injury
Expand Tier I Human GO 3318 Genes GS209452: GO:0006810 transport
Expand Tier I Human GO 4719 Genes GS195977: GO:0007154 cell communication
Expand Tier I Human GO 735 Genes GS204608: GO:0019226 transmission of nerve impulse
Expand Tier I Human GO 35 Genes GS204852: GO:0005272 sodium channel activity
Expand Tier I Human 70 Genes GS175064: HP:0000975 Hyperhidrosis
Expand Tier I Human 913 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Human GO 4371 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Human CTD 101 Genes GS123157: Carbamazepine interacting genes (MeSH:D002220) in CTD
Expand Tier I Human 123 Genes GS176258: HP:0004370 Abnormality of temperature regulation
Expand Tier I Human GO 5605 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 109 Genes GS174136: HP:0002014 Diarrhea
Expand Tier I Human 384 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Human GO 6585 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human GO 50 Genes GS197647: GO:0033555 multicellular organismal response to stress
Expand Tier I Human GO 980 Genes GS198214: GO:0022892 substrate-specific transporter activity
Expand Tier I Human CTD 1522 Genes GS124579: Selenium interacting genes (MeSH:D012643) in CTD
Expand Tier I Human GO 15 Genes GS201108: GO:0005248 voltage-gated sodium channel activity
Expand Tier I Human 1 Genes GS175271: HP:0200026 Ocular pain
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human GO 3372 Genes GS194459: GO:0051234 establishment of localization
Expand Tier I Human GO 17 Genes GS198190: GO:0034706 sodium channel complex
Expand Tier I Human 397 Genes GS171067: HP:0002664 Neoplasm
Expand Tier I Human 16 Genes GS172127: HP:0000632 Lacrimation abnormality
Expand Tier I Human 187 Genes GS173355: HP:0002205 Recurrent respiratory infections
Expand Tier I Human 348 Genes GS176615: HP:0000277 Abnormality of the mandible
Expand Tier I Human GO 178 Genes GS201111: GO:0005244 voltage-gated ion channel activity
Expand Tier I Human GO 226 Genes GS196074: GO:0009636 response to toxin
Expand Tier I Human 19 Genes GS171265: HP:0002633 Vasculitis
Expand Tier I Human CTD 11 Genes GS127224: Tetrodotoxin interacting genes (MeSH:D013779) in CTD
Expand Tier I Human 162 Genes GS175556: HP:0011675 Arrhythmia
Expand Tier I Human 17 Genes GS176514: HP:0007328 Impaired pain sensation
Expand Tier I Human 4 Genes GS171889: HP:0000622 Blurred vision
Expand Tier I Human 397 Genes GS173137: HP:0011821 Abnormality of facial skeleton
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 6151 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human GO 631 Genes GS209611: GO:0055082 cellular chemical homeostasis
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human GO 4034 Genes GS208978: GO:0043169 cation binding
Expand Tier I Human 741 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 85 Genes GS176626: HP:0001909 Leukemia
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 1236 Genes GS202899: GO:0050877 neurological system process
Expand Tier I Human 15 Genes GS171025: HP:0011146 Dialeptic seizures
Expand Tier I Human 567 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human GO 964 Genes GS209451: GO:0006811 ion transport
Expand Tier I Human 15 Genes GS175448: HP:0007359 Focal seizures
Expand Tier I Human CTD 1551 Genes GS125506: Valproic Acid interacting genes (MeSH:D014635) in CTD
Expand Tier I Human 27 Genes GS175187: HP:0002069 Generalized tonic-clonic seizures
Expand Tier I Human GO 786 Genes GS195226: GO:0015075 ion transmembrane transporter activity
Expand Tier I Human GO 4567 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human 11 Genes GS176288: HP:0002121 Absence seizures
Expand Tier I Human CTD 1 Genes GS126739: Saxitoxin interacting genes (MeSH:D012530) in CTD
Expand Tier I Human 197 Genes GS174756: HP:0011947 Respiratory tract infection
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 44 Genes GS173157: HP:0003326 Myalgia