Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
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- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: C2h4orf3 ENSRNOG00000014654

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Description

similar to human chromosome 4 open reading frame 3 [Source:RGD Symbol;Acc:1594660]

Gene Synonyms

LOC691807, MGC112638

Location

Primary_assembly 2: 213,740,525-213,742,952 forward strand.

GRCr8:CM070392.1

About this gene

This gene has 1 transcript (splice variant) and 87 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000019647.4	C2h4orf3-201	1671	65aa	ENSRNOP00000019647.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HVH5 Q498U0	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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Gene tree

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