Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
Pathway
Molecular interactions
External references
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ID History
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Gene: C5h9orf152 ENSRNOG00000012068

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Description

similar to human chromosome 9 open reading frame 152 [Source:RGD Symbol;Acc:1589037]

Gene Synonyms

LOC685849

Location

Primary_assembly 5: 77,455,710-77,463,069 reverse strand.

GRCr8:CM070395.1

About this gene

This gene has 1 transcript (splice variant) and 111 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000016068.7	C5h9orf152-201	3120	234aa	ENSRNOP00000016068.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6KDU0 D4A4N9	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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