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: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: C10h17orf58 ENSRNOG00000043295

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Description

similar to human chromosome 17 open reading frame 58 [Source:RGD Symbol;Acc:1565033]

Gene Synonyms

LOC498014, RGD1565033

Location

Primary_assembly 10: 92,471,934-92,477,330 forward strand.

GRCr8:CM070400.1

About this gene

This gene has 2 transcripts (splice variants) and 185 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000143645.1	C10h17orf58-202	2367	490aa	ENSRNOP00000099375.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000065589.3	C10h17orf58-201	1965	356aa	ENSRNOP00000063842.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZWY4	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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