Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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- GO: Anatomical entity
Phenotypes
Genetic Variation
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Gene: Rnf146 ENSRNOG00000011588

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Description

ring finger protein 146 [Source:RGD Symbol;Acc:1306482]

Gene Synonyms

LOC308051

Location

Primary_assembly 1: 30,287,511-30,304,361 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants), 272 orthologues and is associated with 2 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000015421.8	Rnf146-201	1962	355aa	ENSRNOP00000015421.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A140TAB2	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 P4: Where the APPRIS core modules are unable to choose a clear principal CDS and there is more than one variant with a distinct (but consecutive) CCDS identifiers, APPRIS selects the longest CCDS isoform as the principal variant. 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 P4,
ENSRNOT00000119984.2	Rnf146-202	1869	352aa	ENSRNOP00000081042.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5XIK5	APPRIS ALT1: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that is conserved in at least three tested species. 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 ALT1,

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Summary

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