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

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Gene: RNF139 ENSSSCG00000024412

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Description

ring finger protein 139 [Source:HGNC Symbol;Acc:HGNC:17023]

Location

Primary_assembly 4: 15,154,331-15,197,511 reverse strand.

Sscrofa11.1:CM000815.5

About this gene

This gene has 3 transcripts (splice variants), 205 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000027560.3	RNF139-202	8030	665aa	ENSSSCP00000027691.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D0ZJ16 I3LU92	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,
ENSSSCT00000030960.5	RNF139-203	5134	651aa	ENSSSCP00000025132.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D1CT42 I3LM12	-
ENSSSCT00000071362.2	RNF139-201	4013	439aa	ENSSSCP00000068489.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1T0W0 A0A5G2RCU6	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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