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
  - Paralogues
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: EMSY ENSBTAG00000010826

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Description

EMSY transcriptional repressor, BRCA2 interacting [Source:VGNC Symbol;Acc:VGNC:28484]

Location

Primary_assembly 15: 55,852,806-55,933,677 forward strand.

ARS-UCD2.0:CM008182.2

About this gene

This gene has 9 transcripts (splice variants) and 210 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000081876.3	EMSY-208	5827	1337aa	ENSBTAP00000068424.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1NAY2	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,
ENSBTAT00000075680.3	EMSY-201	5913	1286aa	ENSBTAP00000066665.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M8A4	-
ENSBTAT00000072455.3	EMSY-209	5785	1323aa	ENSBTAP00000061711.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LWB7	-
ENSBTAT00000066874.2	EMSY-202	5651	1220aa	ENSBTAP00000073985.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MI67	-
ENSBTAT00000014362.8	EMSY-203	5444	1323aa	ENSBTAP00000014362.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1N4A6	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,
ENSBTAT00000084002.3	EMSY-204	5315	1280aa	ENSBTAP00000060839.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LYV7	-
ENSBTAT00000101098.2	EMSY-205	5168	1231aa	ENSBTAP00000082202.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9S834	-
ENSBTAT00000093447.2	EMSY-206	5162	1229aa	ENSBTAP00000100769.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TQX7	-
ENSBTAT00000071041.3	EMSY-207	5147	1224aa	ENSBTAP00000067280.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M1P4	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,

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Summary

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