CHKB-CPT1B readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41998]
Chromosome 22: 50,568,869-50,582,965 reverse strand.
This gene has 3 transcripts (splice variants) Show transcript tableHide transcript table
|CHKB-CPT1B-001||ENST00000453634||2816 bp||60 aa (view)||
Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins.
|-||H3BT56||CDS 5' incomplete5' truncation in transcript evidence prevents annotation of the start of the CDS.GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).|
|CHKB-CPT1B-002||ENST00000452668||546 bp||No protein product||
Processed transcriptTranscripts that don't contain an open reading frame (ORF) and cannot be placed in one of the other categories.
|CHKB-CPT1B-003||ENST00000492556||4906 bp||No protein product||
Retained intronAlternatively spliced transcript that is believed to contain intronic sequence relative to other coding transcripts in a given locus.