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
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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: C4h2orf42 ENSRNOG00000017380

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Description

similar to human chromosome 2 open reading frame 42 [Source:RGD Symbol;Acc:1306746]

Gene Synonyms

LOC312511, RGD1306746

Location

Primary_assembly 4: 120,445,830-120,474,396 forward strand.

GRCr8:CM070394.1

About this gene

This gene has 1 transcript (splice variant) and 188 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000023654.7	C4h2orf42-201	2730	574aa	ENSRNOP00000023654.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6IAX1 F7FFR6	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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