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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 ENSG00000170881

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Description

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

Gene Synonyms

HRCA1, RCA1, TRC8

Location

Chromosome 8: 125,486,979-125,500,155 forward strand.

GRCh37:CM000670.1

About this gene

This gene has 2 transcripts (splice variants), 3 paralogues and is associated with 2 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000303545.3	RNF139-001	2637	664aa	ENSP00000304051.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS6350	E5RH85 Q8WU17	NM_007218.3	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000517684.2	RNF139-002	467	68aa	ENSP00000429836.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		E5RH85	-	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,

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Summary

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