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: C11H2orf68 ENSBTAG00000018291

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Description

chromosome 11 C2orf68 homolog [Source:VGNC Symbol;Acc:VGNC:52617]

Location

Primary_assembly 11: 49,394,035-49,403,916 forward strand.

ARS-UCD1.3:CM008178.2

About this gene

This gene has 3 transcripts (splice variants) and 192 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000092880.1	C11H2orf68-201	1919	305aa	ENSBTAP00000088836.1	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,
ENSBTAT00000024344.4	C11H2orf68-203	1584	147aa	ENSBTAP00000024344.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A4IFR8	-
ENSBTAT00000076335.2	C11H2orf68-202	1564	166aa	ENSBTAP00000062359.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M2M2	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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