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: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: C3orf38 ENSSSCG00000034645

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Description

chromosome 13 C3orf38 homolog [Source:VGNC Symbol;Acc:VGNC:85934]

Location

Primary_assembly 13: 167,789,645-167,803,754 reverse strand.

Sscrofa11.1:CM000824.5

About this gene

This gene has 2 transcripts (splice variants) and 214 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000039968.3	C3orf38-201	1378	327aa	ENSSSCP00000032350.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A286ZLK8 A0A4X1UJ82	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,
ENSSSCT00000059044.3	C3orf38-202	9061	311aa	ENSSSCP00000033567.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A286ZQ22 A0A8D1BW86	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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