Snapgene viewer abi reference sequence download#

Vertebrate Genome Annotation (VEGA) database.The Weizmann Institute of Science GeneCards and MalaCards databases.PhosphoSitePlusВ® - comprehensive post-translational modification resource.Annotated Pharmacogenomic Information for KCNQ1.Kyoto Encyclopedia of Genes and Genomes.GenScript latest version of gene cDNA ORF Clone.BioGRID CRISPR Screen Phenotypes (12 hits/1070 screens).BioGRID Open Repository of CRISPR Screens (ORCS).RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119 Location: 384 в†’ 490 KCNQ_channel KCNQ voltage-gated potassium channel Location: 2 в†’ 232 Ion_trans Ion transport protein pfam03520 The resulting shorter isoform (2) has a distinct N-terminus compared to isoform 1. Status: REVIEWED Description Transcript Variant: This variant (2) contains an alternate 5' terminal exon and initiates translation from an alternate start site compared to variant 1. See identical proteins and their annotated locations for NP_861463.1 NM_181798.1 в†’ NP_861463.1 potassium voltage-gated channel subfamily KQT member 1 isoform 2 precursor Location: 270 в†’ 349 Ion_trans_2 Ion channel Location: 511 в†’ 617 KCNQ_channel KCNQ voltage-gated potassium channel pfam07885 Location: 153 в†’ 359 Ion_trans Ion transport protein pfam03520 Status: REVIEWED Description Transcript Variant: This variant (1) encodes the longer isoform (1). See identical proteins and their annotated locations for NP_000209.2 NM_000218.3 в†’ NP_000209.2 potassium voltage-gated channel subfamily KQT member 1 isoform 1

Snapgene viewer abi reference sequence download#

NG_008935.1В RefSeqGene Range 5001.409120 Download GenBank, FASTA, Sequence Viewer (Graphics), LRG_287 This section to the one reported in Genomic regions, Identify version mismatches by comparing the version of the RefSeq in These reference sequences are curated independently of the genomeДЄnnotation cycle, so their versions may not match the RefSeq versions in the current These reference sequences exist independently of genome builds. Expression Broad expression in adrenal (RPKM 44.1), thyroid (RPKM 34.9) and 16 other tissues See more Orthologs mouse all NEW Try the new Gene table Alternatively spliced transcript variants have been found for this gene. This gene is located in a region of chromosome 11 amongst other imprinted genes that are associated with Beckwith-Wiedemann syndrome (BWS), and itself has been shown to be disrupted by chromosomal rearrangements in patients with BWS. This gene exhibits tissue-specific imprinting, with preferential expression from the maternal allele in some tissues, and biallelic expression in others. Mutations in this gene are associated with hereditary long QT syndrome 1 (also known as Romano-Ward syndrome), Jervell and Lange-Nielsen syndrome, and familial atrial fibrillation. This protein can form heteromultimers with two other potassium channel proteins, KCNE1 and KCNE3. Database of Single Nucleotide Polymorphisms (dbSNP)ДЇull Name potassium voltage-gated channel subfamily Q member 1 provided by HGNC Primary source HGNC:HGNC:6294 See related Ensembl:ENSG00000053918 MIM:607542 Gene type protein coding RefSeq status REVIEWED Organism Homo sapiens Lineage Eukaryota Metazoa Chordata Craniata Vertebrata Euteleostomi Mammalia Eutheria Euarchontoglires Primates Haplorrhini Catarrhini Hominidae Homo Also known as LQT RWS WRS LQT1 SQT2 ATFB1 ATFB3 JLNS1 KCNA8 KCNA9 Kv1.9 Kv7.1 KVLQT1 Summary This gene encodes a voltage-gated potassium channel required for repolarization phase of the cardiac action potential.Database of Genomic Structural Variation (dbVar).Online Mendelian Inheritance in Man (OMIM).Database of Genotypes and Phenotypes (dbGaP).Structure (Molecular Modeling Database).Conserved Domain Search Service (CD Search).BLAST (Basic Local Alignment Search Tool).