Description
potassium channel, subfamily T, member 1 [Source:HGNC Symbol;Acc:18865]
Location
Chromosome 9: 138,594,031-138,684,992 forward strand.
Transcripts
This gene has 12 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
KCNT1-001ENST000004876644695ENSP000004178511211Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
KCNT1-002ENST000003717574717ENSP000003608221235Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS35175
KCNT1-004ENST000004918063789ENSP000004190861223Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
KCNT1-005ENST000004884443725ENSP000004190071237Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
KCNT1-006ENST000004903553711ENSP000004180031235Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
KCNT1-007ENST000004865773720ENSP000004175781215Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
KCNT1-010ENST000004739411024ENSP00000420764285Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
KCNT1-201ENST000002636044678ENSP000002636041230Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
KCNT1-202ENST000002984804830ENSP000002984801256Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
KCNT1-003ENST000004607504738ENSP00000418777122Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
KCNT1-008ENST000004750083999No protein product-Retained intronNoncoding transcript containing intronic sequence. -
KCNT1-009ENST000004903634065No protein product-Retained intronNoncoding transcript containing intronic sequence. -

Transcript and Gene level displays

In Archive EnsEMBL we provide displays at two levels:

  • Transcript views which provide information specific to an individual transcript such as the cDNA and CDS sequences and protein domain annotation.
  • Gene views which provide displays for data associated at the gene level such as orthologues, paralogues, regulatory regions and splice variants.

This view is a gene level view. To access the transcript level displays select a Transcript ID in the table above and then navigate to the information you want using the menu at the left hand side of the page. To return to viewing gene level information click on the Gene tab in the menu bar at the top of the page.