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: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: C13H20orf96 ENSBTAG00000002115

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Description

chromosome 13 C20orf96 homolog [Source:VGNC Symbol;Acc:VGNC:49173]

Location

Primary_assembly 13: 60,720,562-60,744,561 forward strand.

ARS-UCD1.3:CM008180.2

About this gene

This gene has 3 transcripts (splice variants) and 87 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000114118.1	C13H20orf96-202	2312	367aa	ENSBTAP00000093466.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSBTAT00000123956.1	C13H20orf96-203	2181	326aa	ENSBTAP00000090108.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000002731.6	C13H20orf96-201	1429	361aa	ENSBTAP00000002731.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1N466	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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