pyrimidinergic receptor P2Y6 [Source:VGNC Symbol;Acc:VGNC:91128]
Primary_assembly 9: 7,749,375-7,759,721 forward strand.
Sscrofa11.1:CM000820.5
This gene has 4 transcripts (splice variants), 182 orthologues and 13 paralogues.
| Transcript ID | Name | bp | Protein | Translation ID | Biotype | UniProt Match | Flags |
|---|---|---|---|---|---|---|---|
| ENSSSCT00000070273.2 | P2RY6-203 | 2806 | 370aa | ENSSSCP00000064175.2 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0A5G2QIC7 | 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, |
| ENSSSCT00000016175.3 | P2RY6-202 | 1551 | 330aa | ENSSSCP00000015742.2 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0A8D1X4I6 F1SUT5 | 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, |
| ENSSSCT00000082074.2 | P2RY6-204 | 1524 | 330aa | ENSSSCP00000069522.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0A8D1X4I6 F1SUT5 | 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, |
| ENSSSCT00000087607.2 | P2RY6-201 | 1493 | 330aa | ENSSSCP00000072777.2 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0A8D1X4I6 F1SUT5 | 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, |
