Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
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: C3h20orf173 ENSRNOG00000047596

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Description

similar to human chromosome 20 open reading frame 173 [Source:RGD Symbol;Acc:7514905]

Gene Synonyms

AC118414.2, LOC100359643, LOC102550306

Location

Primary_assembly 3: 164,980,014-164,985,029 reverse strand.

GRCr8:CM070393.1

About this gene

This gene has 1 transcript (splice variant), 312 orthologues and 14 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000071825.3	C3h20orf173-201	784	194aa	ENSRNOP00000065197.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M0R6Y4	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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