TIAM Rac1 associated GEF 2a [Source:ZFIN;Acc:ZDB-GENE-030219-98]
id:ibd5033
Chromosome 17: 49,127,003-49,137,210 forward strand.
This transcript has 6 exons, is annotated with 9 domains and features, is associated with 318 variant alleles and maps to 21 oligo probes.
This transcript is a product of gene ENSDARG00000087780.5 Show transcript tableHide transcript table
| Transcript ID | Name | bp | Protein | Translation ID | Biotype | UniProt Match | Flags |
|---|---|---|---|---|---|---|---|
| ENSDART00000179545.2 | tiam2a-205 | 5583 | 1671aa | ENSDARP00000143722.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0A286Y9S9 | 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 P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms as 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 P5, |
| ENSDART00000156492.3 | tiam2a-201 | 6529 | 1652aa | ENSDARP00000128035.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0A286YAC4 | 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, |
| ENSDART00000177166.2 | tiam2a-203 | 5106 | 1671aa | ENSDARP00000143330.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0A286Y9S9 | APPRIS P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms as 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 P5, |
| ENSDART00000177390.2 | tiam2a-204 | 5049 | 1652aa | ENSDARP00000144119.2 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0A286YAC4 | 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, |
| ENSDART00000185900.1 | tiam2a-206 | 4843 | 1611aa | ENSDARP00000145119.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0A2R8Q2X5 | - |
| ENSDART00000190114.1 | tiam2a-207 | 4716 | 1541aa | ENSDARP00000155324.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0A2R8QJ89 | 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, |
| ENSDART00000157360.2 | tiam2a-202 | 558 | 186aa | ENSDARP00000128355.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | X1WDQ6 | 5' and 3' truncations in transcript evidence prevent annotation of the start and the end of the CDS.CDS 5' and 3' incomplete, |