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: Anatomical entity
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: C2h4orf33 ENSRNOG00000038330

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Description

similar to human chromosome 4 open reading frame 33 [Source:RGD Symbol;Acc:1359508]

Gene Synonyms

MGC109006, RGD1359508

Location

Primary_assembly 2: 126,697,854-126,746,878 forward strand.

GRCr8:CM070392.1

About this gene

This gene has 2 transcripts (splice variants) and 214 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000114451.2	C2h4orf33-202	963	199aa	ENSRNOP00000085480.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A1R0 A6II61	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,
ENSRNOT00000058366.4	C2h4orf33-201	734	115aa	ENSRNOP00000055168.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6II63 Q5M845	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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