Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
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: C1h11orf24 ENSRNOG00000025245

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Description

similar to human chromosome 11 open reading frame 24 [Source:RGD Symbol;Acc:1311946]

Gene Synonyms

LOC309145, MGC116211, RGD1311946

Location

Primary_assembly 1: 210,374,543-210,383,566 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 1 transcript (splice variant), 154 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000034240.7	C1h11orf24-201	2486	448aa	ENSRNOP00000037591.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q4V7A5	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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