Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Biological process
- GO: Cellular component
- GO: Molecular function
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
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Gene: Brd8 ENSRNOG00000020340

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Description

bromodomain containing 8 [Source:RGD Symbol;Acc:1307003]

Gene Synonyms

LOC291691, p120

Location

Primary_assembly 18: 26,455,512-26,504,006 reverse strand.

GRCr8:CM070408.1

About this gene

This gene has 6 transcripts (splice variants), 216 orthologues and is associated with 2 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000101754.2	Brd8-204	4282	1206aa	ENSRNOP00000095490.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ATL0	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 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,
ENSRNOT00000034385.7	Brd8-201	4063	1133aa	ENSRNOP00000033259.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1M858	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,
ENSRNOT00000048752.5	Brd8-202	3830	936aa	ENSRNOP00000050917.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E9PTN1	-
ENSRNOT00000118939.2	Brd8-206	3548	999aa	ENSRNOP00000076647.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5Y6W9	-
ENSRNOT00000087968.3	Brd8-203	3133	927aa	ENSRNOP00000069953.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JWN9	-
ENSRNOT00000106891.2	Brd8-205	3013	881aa	ENSRNOP00000095492.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AR97	-

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Summary

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