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: Molecular function
- GO: Cellular component
- GO: Biological process
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: C5h1orf141 ENSRNOG00000022890

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Description

similar to human chromosome 1 open reading frame 141 [Source:RGD Symbol;Acc:1562532]

Gene Synonyms

LOC500513, RGD1562532

Location

Primary_assembly 5: 123,229,916-123,293,251 reverse strand.

GRCr8:CM070395.1

About this gene

This gene has 2 transcripts (splice variants) and 71 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000030112.7	C5h1orf141-201	2181	441aa	ENSRNOP00000035060.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E9PT12	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,
ENSRNOT00000119912.2	C5h1orf141-202	1060	286aa	ENSRNOP00000087159.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GFR2	-

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Summary

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