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- NCIT_C190836 IAO_0000115 "Human KCNT1 wild-type allele is located in the vicinity of 9q34.3 and is approximately 93 kb in length. This allele, which encodes potassium channel subfamily T member 1 protein, is involved in ion conductance and developmental signaling. Mutation of the gene is associated with developmental and epileptic encephalopathy 14 and nocturnal frontal lobe epilepsy 5." @default.
- NCIT_C190836 NCIT_NHC0 "C190836" @default.
- NCIT_C190836 NCIT_P100 "608167" @default.
- NCIT_C190836 NCIT_P102 "AB037843" @default.
- NCIT_C190836 NCIT_P106 "Gene or Genome" @default.
- NCIT_C190836 NCIT_P108 "KCNT1 wt Allele" @default.
- NCIT_C190836 NCIT_P208 "CL1799301" @default.
- NCIT_C190836 NCIT_P321 "57582" @default.
- NCIT_C190836 NCIT_R37 NCIT_C17710 @default.
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- NCIT_C190836 NCIT_R37 NCIT_C19950 @default.
- NCIT_C190836 NCIT_R37 NCIT_C19986 @default.
- NCIT_C190836 NCIT_R37 NCIT_C20139 @default.
- NCIT_C190836 NCIT_R37 NCIT_C20480 @default.
- NCIT_C190836 NCIT_R37 NCIT_C21079 @default.
- NCIT_C190836 NCIT_R37 NCIT_C21124 @default.
- NCIT_C190836 NCIT_R37 NCIT_C21591 @default.
- NCIT_C190836 NCIT_R37 NCIT_C28498 @default.
- NCIT_C190836 NCIT_R37 NCIT_C40515 @default.
- NCIT_C190836 NCIT_R37 NCIT_C40530 @default.
- NCIT_C190836 NCIT_R37 NCIT_C40536 @default.
- NCIT_C190836 NCIT_R37 NCIT_C40792 @default.
- NCIT_C190836 NCIT_R40 NCIT_C12219 @default.
- NCIT_C190836 NCIT_R40 NCIT_C13282 @default.
- NCIT_C190836 NCIT_R40 NCIT_C13377 @default.
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- NCIT_C190836 NCIT_R40 NCIT_C13446 @default.
- NCIT_C190836 NCIT_R40 NCIT_C13828 @default.
- NCIT_C190836 NCIT_R40 NCIT_C14135 @default.
- NCIT_C190836 NCIT_R40 NCIT_C32221 @default.
- NCIT_C190836 NCIT_R40 NCIT_C34070 @default.
- NCIT_C190836 NCIT_R41 NCIT_C14182 @default.
- NCIT_C190836 NCIT_R41 NCIT_C14225 @default.
- NCIT_C190836 NCIT_R41 NCIT_C14234 @default.
- NCIT_C190836 NCIT_R41 NCIT_C14250 @default.
- NCIT_C190836 NCIT_R41 NCIT_C14262 @default.
- NCIT_C190836 NCIT_R41 NCIT_C14282 @default.
- NCIT_C190836 NCIT_R41 NCIT_C25796 @default.
- NCIT_C190836 NCIT_R41 NCIT_C79740 @default.
- NCIT_C190836 normalizedInformationContent "100" @default.
- NCIT_C190836 referenceCount "1" @default.
- NCIT_C190836 hasExactSynonym "DEE14" @default.
- NCIT_C190836 hasExactSynonym "EIEE14" @default.
- NCIT_C190836 hasExactSynonym "ENFL5" @default.
- NCIT_C190836 hasExactSynonym "KCNT1 wt Allele" @default.
- NCIT_C190836 hasExactSynonym "KCa4.1" @default.
- NCIT_C190836 hasExactSynonym "KIAA1422" @default.
- NCIT_C190836 hasExactSynonym "Potassium Channel, Sodium Activated Subfamily T, Member 1 Gene" @default.
- NCIT_C190836 hasExactSynonym "Potassium Channel, Subfamily T, Member 1 Gene" @default.
- NCIT_C190836 hasExactSynonym "Potassium Sodium-Activated Channel Subfamily T Member 1 wt Allele" @default.
- NCIT_C190836 hasExactSynonym "SLACK" @default.
- NCIT_C190836 hasExactSynonym "Sequence Like A Calcium-Activated K+ Channel Gene" @default.
- NCIT_C190836 hasExactSynonym "Slo2.2" @default.
- NCIT_C190836 hasExactSynonym "bA100C15.2" @default.
- NCIT_C190836 type Class @default.
- NCIT_C190836 isDefinedBy ncit.owl @default.
- NCIT_C190836 label "KCNT1 wt Allele" @default.
- NCIT_C190836 subClassOf B6196e5c14c0a2fb0a87eb08dd082b84b @default.
- NCIT_C190836 subClassOf B71ff4882017db46eab65eb58933aca00 @default.
- NCIT_C190836 subClassOf NCIT_C16612 @default.
- NCIT_C190836 subClassOf NCIT_C190835 @default.
- NCIT_C190836 subClassOf NCIT_C190836 @default.
- NCIT_C190836 subClassOf NCIT_C21295 @default.
- NCIT_C190836 subClassOf NCIT_C25869 @default.
- NCIT_C190836 subClassOf NCIT_C25993 @default.
- NCIT_C190836 subClassOf NCIT_C26039 @default.
- NCIT_C190836 subClassOf NCIT_C28533 @default.