Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Cellular component
- GO: Biological process
- GO: Molecular function
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: C5orf34 ENSSSCG00000016876

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Description

chromosome 16 C5orf34 homolog [Source:VGNC Symbol;Acc:VGNC:108008]

Location

Primary_assembly 16: 28,058,264-28,094,452 reverse strand.

Sscrofa11.1:CM000827.5

About this gene

This gene has 2 transcripts (splice variants) and 174 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000077317.2	C5orf34-202	3450	613aa	ENSSSCP00000060014.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2Q7G0	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,
ENSSSCT00000018380.4	C5orf34-201	1316	187aa	ENSSSCP00000017884.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1SMG4	-

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Summary

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