Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: C8h11orf87 ENSRNOG00000025463

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Description

similar to human chromosome 11 open reading frame 87 [Source:RGD Symbol;Acc:1642426]

Gene Synonyms

LOC100125362, MGC109299

Location

Primary_assembly 8: 61,957,676-61,968,365 reverse strand.

GRCr8:CM070398.1

About this gene

This gene has 2 transcripts (splice variants) and 175 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000114873.2	C8h11orf87-202	10554	196aa	ENSRNOP00000094101.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6J4I6 Q569A3	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,
ENSRNOT00000028972.5	C8h11orf87-201	9442	196aa	ENSRNOP00000062036.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6J4I6 Q569A3	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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