solute carrier family 17 (sodium phosphate), member 4 [Source:MGI Symbol;Acc:MGI:2442850]
9130214H05Rik
Chromosome 13: 24,079,873-24,098,992 reverse strand.
GRCm39:CM001006.3
This gene has 5 transcripts (splice variants), 397 orthologues and 12 paralogues.
| Transcript ID | Name | bp | Protein | Translation ID | Biotype | CCDS | UniProt Match | Flags |
|---|---|---|---|---|---|---|---|---|
| ENSMUST00000021769.16 | Slc17a4-201 | 1604 | 492aa | ENSMUSP00000021769.10 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | CCDS49221 | Q5NCM1 | 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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1,TSL 5: A transcript where no single transcript supports the model structure. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:5, |
| ENSMUST00000110407.4 | Slc17a4-202 | 2177 | 452aa | ENSMUSP00000106037.4 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0A2C9F2D4 | The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1, | |
| ENSMUST00000225797.2 | Slc17a4-205 | 4394 | 254aa | ENSMUSP00000153087.2 | Nonsense mediated decay | A0A286YCP3 | - | |
| ENSMUST00000225763.2 | Slc17a4-204 | 3527 | No protein | - | An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron | - | - | |
| ENSMUST00000224360.2 | Slc17a4-203 | 2525 | No protein | - | An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron | - | - |
