Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: RNF8 ENSBTAG00000008321

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Description

ring finger protein 8 [Source:VGNC Symbol;Acc:VGNC:34073]

Location

Primary_assembly 23: 11,245,209-11,289,017 forward strand.

ARS-UCD2.0:CM008190.2

About this gene

This gene has 7 transcripts (splice variants) and 189 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000081781.3	RNF8-203	1759	490aa	ENSBTAP00000070917.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAF7AKR0	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 ALT2: 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 appear to be conserved in fewer than 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 ALT2,
ENSBTAT00000095946.2	RNF8-201	2379	465aa	ENSBTAP00000096023.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TBC7	-
ENSBTAT00000093085.2	RNF8-202	2069	487aa	ENSBTAP00000095665.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q2HJ46	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be 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 P2,
ENSBTAT00000082469.3	RNF8-205	1946	466aa	ENSBTAP00000074154.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MQ87	APPRIS ALT2: 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 appear to be conserved in fewer than 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 ALT2,
ENSBTAT00000109431.2	RNF8-204	1924	444aa	ENSBTAP00000103597.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9U1E0	-
ENSBTAT00000070532.3	RNF8-206	1901	451aa	ENSBTAP00000059060.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LPX0	-
ENSBTAT00000010959.5	RNF8-207	1380	459aa	ENSBTAP00000010959.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A452DI91	-

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Summary

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