microfibril associated protein 5 [Source:VGNC Symbol;Acc:VGNC:90177]
Primary_assembly 5: 62,742,319-62,757,519 forward strand.
Sscrofa11.1:CM000816.5
This gene has 6 transcripts (splice variants), 184 orthologues and 1 paralogue.
| Transcript ID | Name | bp | Protein | Translation ID | Biotype | UniProt Match | Flags |
|---|---|---|---|---|---|---|---|
| ENSSSCT00000081063.2 | MFAP5-205 | 1097 | 236aa | ENSSSCP00000071547.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0A5G2R2Y0 A0A8D0WIR8 | 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, |
| ENSSSCT00000096756.1 | MFAP5-204 | 1085 | 142aa | ENSSSCP00000080578.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0A8D1L6C2 A0A8W4FQD2 | - |
| ENSSSCT00000093860.1 | MFAP5-206 | 1061 | 224aa | ENSSSCP00000077580.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0A8W4FGZ2 | - |
| ENSSSCT00000094867.1 | MFAP5-202 | 989 | 158aa | ENSSSCP00000080132.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0A5G2R964 A0A8D1ALR9 | - |
| ENSSSCT00000074791.1 | MFAP5-203 | 959 | 148aa | ENSSSCP00000074050.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0A5G2RMX9 | - |
| ENSSSCT00000000722.5 | MFAP5-201 | 927 | 154aa | ENSSSCP00000000707.5 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0A8D0QYY2 F1SLW6 | 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, |
