sorting nexin 17 [Source:RGD Symbol;Acc:1306424]
LOC298836
Primary_assembly 6: 30,897,501-30,902,972 reverse strand.
GRCr8:CM070396.1
This gene has 3 transcripts (splice variants), 207 orthologues, 2 paralogues and is associated with 2 phenotypes.
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sorting nexin 17 [Source:RGD Symbol;Acc:1306424]
LOC298836
Primary_assembly 6: 30,897,501-30,902,972 reverse strand.
GRCr8:CM070396.1
This gene has 3 transcripts (splice variants), 207 orthologues, 2 paralogues and is associated with 2 phenotypes.
Transcript ID | Name | bp | Protein | Translation ID | Biotype | UniProt Match | Flags |
---|---|---|---|---|---|---|---|
ENSRNOT00000115042.2 | Snx17-202 | 2062 | 556aa | ENSRNOP00000082948.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0A8I6GA49 | 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, |
ENSRNOT00000091264.3 | Snx17-201 | 1909 | 470aa | ENSRNOP00000070417.3 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0A0G2JXV4 A6HA69 Q6AYS6 | - |
ENSRNOT00000118894.2 | Snx17-203 | 1885 | 462aa | ENSRNOP00000095437.2 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0A8I6AMM3 | 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, |
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