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
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Gene: Rnf222 ENSRNOG00000022964

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Description

ring finger protein 222 [Source:RGD Symbol;Acc:1310573]

Gene Synonyms

LOC363627, RGD1310573

Location

Primary_assembly 10: 54,090,131-54,102,119 forward strand.

GRCr8:CM070400.1

About this gene

This gene has 4 transcripts (splice variants) and 174 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000150652.1	Rnf222-203	5217	211aa	ENSRNOP00000099699.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HFL3	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,
ENSRNOT00000154956.1	Rnf222-204	3138	211aa	ENSRNOP00000100816.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HFL3	-
ENSRNOT00000135124.1	Rnf222-202	2952	211aa	ENSRNOP00000100987.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HFL3	-
ENSRNOT00000038454.5	Rnf222-201	2755	211aa	ENSRNOP00000032127.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HFL3 D3ZTZ3	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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