- FSIP2-AS1 [Search on AGR]
Homo sapiens ASSOCIATED WITH genetic disease; long QT syndrome; Prolonged QT interval
- CACNA1C-AS4 [Search on AGR]
Homo sapiens ASSOCIATED WITH Hyperphosphatemic Familial Tumoral Calcinosis 1; long QT syndrome; Prolonged QT interval
- C20orf144 [Search on AGR]
Homo sapiens ASSOCIATED WITH genetic disease; long QT syndrome; Prolonged QT interval; INTERACTS WITH cadmium atom; cisplatin; valproic acid
- CACNA1C-AS2 [Search on AGR]
Homo sapiens ASSOCIATED WITH Hyperphosphatemic Familial Tumoral Calcinosis 1; long QT syndrome; Prolonged QT interval; INTERACTS WITH sodium arsenite
- CACNA1C-IT3 [Search on AGR]
Homo sapiens ASSOCIATED WITH Hyperphosphatemic Familial Tumoral Calcinosis 1; long QT syndrome; Prolonged QT interval; INTERACTS WITH Aflatoxin B2 alpha
- unc-103 [Browse genome (BioProject PRJNA13758)] [Search on AGR]
Caenorhabditis elegans Predicted to enable inward rectifier potassium channel activity. Involved in mating behavior and regulation of muscle contraction. Predicted to be located in plasma membrane. Predicted to be part of monoatomic ion channel complex. Expressed in body wall musculature; neurons; non-striated muscle; and in male. Used to study long QT syndrome. Human ortholog(s) of this gene implicated in long QT syndrome 2 and short QT syndrome. Is an ortholog of human KCNH2 (potassium voltage-gated channel subfamily H member 2) and KCNH7 (potassium voltage-gated channel subfamily H member 7).
- algn-10 [Browse genome (BioProject PRJNA13758)] [Search on AGR]
Caenorhabditis elegans Predicted to enable dolichyl pyrophosphate Glc2Man9GlcNAc2 alpha-1,2-glucosyltransferase activity. Predicted to be involved in protein N-linked glycosylation. Predicted to be located in endoplasmic reticulum. Human ortholog(s) of this gene implicated in long QT syndrome 2. Is an ortholog of human ALG10 (ALG10 alpha-1,2-glucosyltransferase) and ALG10B (ALG10 alpha-1,2-glucosyltransferase B).
- ZNF341-AS1 [Search on AGR]
Homo sapiens ASSOCIATED WITH genetic disease; hyper IgE recurrent infection syndrome 3; long QT syndrome
- PTOV1-AS2 [Search on AGR]
Homo sapiens ASSOCIATED WITH developmental and epileptic encephalopathy 12; genetic disease; long QT syndrome; INTERACTS WITH formaldehyde; sodium arsenite