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

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Gene: C9H6orf118 ENSBTAG00000015485

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Description

chromosome 9 C6orf118 homolog [Source:VGNC Symbol;Acc:VGNC:52744]

Location

Primary_assembly 9: 100,424,185-100,448,242 reverse strand.

ARS-UCD1.3:CM008176.2

About this gene

This gene has 2 transcripts (splice variants) and 118 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000020582.5	C9H6orf118-202	1627	472aa	ENSBTAP00000020582.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q2NL15	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,
ENSBTAT00000081309.2	C9H6orf118-201	1566	464aa	ENSBTAP00000065686.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1N5U7	-

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Summary

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