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

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Gene: C18H16orf86 ENSBTAG00000018906

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Description

chromosome 18 C16orf86 homolog [Source:VGNC Symbol;Acc:VGNC:49177]

Location

Primary_assembly 18: 35,220,254-35,222,184 forward strand.

ARS-UCD2.0:CM008185.2

About this gene

This gene has 1 transcript (splice variant) and 89 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000064305.3	C18H16orf86-201	1246	323aa	ENSBTAP00000053901.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3MWK0	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,

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Summary

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