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: Rnf212 ENSRNOG00000059010

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Description

ring finger protein 212 [Source:RGD Symbol;Acc:1588767]

Gene Synonyms

LOC689721

Location

Primary_assembly 14: 1,093,759-1,169,966 forward strand.

GRCr8:CM070404.1

About this gene

This gene has 4 transcripts (splice variants), 99 orthologues, 1 paralogue and is associated with 6 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000139974.1	Rnf212-203	1252	325aa	ENSRNOP00000102609.1	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,
ENSRNOT00000096364.2	Rnf212-202	2901	118aa	ENSRNOP00000077915.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5XWM3	-
ENSRNOT00000172376.1	Rnf212-204	1227	308aa	ENSRNOP00000099102.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000085898.3	Rnf212-201	988	282aa	ENSRNOP00000070745.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JYP9	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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