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: C17h9orf153 ENSRNOG00000042206

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Description

similar to human chromosome 9 open reading frame 153 [Source:RGD Symbol;Acc:6488044]

Gene Synonyms

LOC100912252, LOC681199

Location

Primary_assembly 17: 4,981,452-4,987,918 forward strand.

GRCr8:CM070407.1

About this gene

This gene has 1 transcript (splice variant) and 43 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000068160.4	C17h9orf153-201	1141	268aa	ENSRNOP00000059484.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6KAH6 D4A951	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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