Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
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ID History
- Gene history

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Gene: C15orf39 ENSSSCG00000001885

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Description

chromosome 7 C15orf39 homolog [Source:VGNC Symbol;Acc:VGNC:86070]

Location

Primary_assembly 7: 58,381,034-58,386,366 reverse strand.

Sscrofa11.1:CM000818.5

About this gene

This gene has 2 transcripts (splice variants) and 114 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000002110.5	C15orf39-202	5331	939aa	ENSSSCP00000002060.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D1GZX6 F1SJ54	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 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,
ENSSSCT00000091342.2	C15orf39-201	5028	939aa	ENSSSCP00000060171.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D1GZX6 F1SJ54	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,

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Summary

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