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: 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: C2h1orf52 ENSRNOG00000014857

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Description

similar to human chromosome 1 open reading frame 52 [Source:RGD Symbol;Acc:1560065]

Gene Synonyms

LOC499724, RGD1560065

Location

Primary_assembly 2: 237,513,711-237,520,346 forward strand.

GRCr8:CM070392.1

About this gene

This gene has 2 transcripts (splice variants) and 205 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000113355.2	C2h1orf52-202	1551	181aa	ENSRNOP00000096146.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AL75	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,
ENSRNOT00000019964.8	C2h1orf52-201	1661	99aa	ENSRNOP00000019964.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4A6E8	-

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Summary

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