Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
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: Rnf126 ENSRNOG00000009028

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Description

ring finger protein 126 [Source:RGD Symbol;Acc:1306011]

Gene Synonyms

LOC314613, MGC124770

Location

Primary_assembly 7: 10,590,039-10,598,132 forward strand.

GRCr8:CM070397.1

About this gene

This gene has 1 transcript (splice variant), 266 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000012317.8	Rnf126-201	2110	338aa	ENSRNOP00000012317.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q499Q1	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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