Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Rnf166 ENSRNOG00000013777

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Description

ring finger protein 166 [Source:RGD Symbol;Acc:1302950]

Gene Synonyms

MGC2647

Location

Primary_assembly 19: 67,437,974-67,447,814 reverse strand.

GRCr8:CM070409.1

About this gene

This gene has 3 transcripts (splice variants), 196 orthologues, 4 paralogues and is associated with 5 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000150083.1	Rnf166-203	1990	266aa	ENSRNOP00000100250.1	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,
ENSRNOT00000135295.1	Rnf166-202	1918	242aa	ENSRNOP00000109733.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000018591.5	Rnf166-201	1755	237aa	ENSRNOP00000018591.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6IZS2 Q6J1I7	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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