toll like receptor 8 [Source:VGNC Symbol;Acc:VGNC:94027]
Primary_assembly X: 9,597,604-9,616,757 forward strand.
Sscrofa11.1:CM000830.5
This gene has 6 transcripts (splice variants), 200 orthologues and 23 paralogues.
| Transcript ID | Name | bp | Protein | Translation ID | Biotype | UniProt Match | Flags |
|---|---|---|---|---|---|---|---|
| ENSSSCT00000075708.2 | TLR8-206 | 6738 | 1061aa | ENSSSCP00000062586.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0A5G2QDA1 A0A8D1I603 | A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS ALT2, |
| ENSSSCT00000033339.4 | TLR8-203 | 6903 | 1028aa | ENSSSCP00000030352.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0A4X1TK68 B3XXC2 | APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P2, |
| ENSSSCT00000073702.2 | TLR8-205 | 6789 | 1028aa | ENSSSCP00000065407.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0A4X1TK68 B3XXC2 | APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P2, |
| ENSSSCT00000064062.3 | TLR8-201 | 6772 | 1028aa | ENSSSCP00000031310.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0A4X1TK68 B3XXC2 | APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P2, |
| ENSSSCT00000013255.5 | TLR8-204 | 6764 | 1028aa | ENSSSCP00000012899.4 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0A4X1TK68 B3XXC2 | APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P2, |
| ENSSSCT00000033711.4 | TLR8-202 | 6714 | 1028aa | ENSSSCP00000030972.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0A4X1TK68 B3XXC2 | APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P2, |
