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
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Molecular interactions
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ID History
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Gene: C10h17orf75 ENSRNOG00000000237

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Description

similar to human chromosome 17 open reading frame 75 [Source:RGD Symbol;Acc:1310429]

Gene Synonyms

LOC303764, RGD1310429

Location

Primary_assembly 10: 65,858,774-65,874,883 reverse strand.

GRCr8:CM070400.1

About this gene

This gene has 1 transcript (splice variant) and 209 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000000254.9	C10h17orf75-201	2683	504aa	ENSRNOP00000000254.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZEJ9	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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