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

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Gene: RNF13 ENSSSCG00000027459

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Description

ring finger protein 13 [Source:VGNC Symbol;Acc:VGNC:92355]

Location

Primary_assembly 13: 90,034,714-90,174,506 forward strand.

Sscrofa11.1:CM000824.5

About this gene

This gene has 3 transcripts (splice variants), 225 orthologues and 8 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000066027.2	RNF13-203	2412	405aa	ENSSSCP00000057759.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D1FWU8 A0A8D1IKH9	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,
ENSSSCT00000072819.1	RNF13-201	2327	148aa	ENSSSCP00000072119.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2RJN3 A0A8D0J7T5	-
ENSSSCT00000099061.1	RNF13-202	2283	363aa	ENSSSCP00000076652.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D0ULG2 A0A8W4FBL1	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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Orthologues

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