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: C8h3orf62 ENSRNOG00000046155

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Description

similar to human chromosome 3 open reading frame 62 [Source:RGD Symbol;Acc:1589651]

Gene Synonyms

LOC498675

Location

Primary_assembly 8: 117,958,576-117,963,201 forward strand.

GRCr8:CM070398.1

About this gene

This gene has 2 transcripts (splice variants) and 94 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000095427.2	C8h3orf62-202	1212	257aa	ENSRNOP00000093480.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AJQ1	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,
ENSRNOT00000075271.3	C8h3orf62-201	1032	251aa	ENSRNOP00000066835.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6I351 M0RBA6	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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