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

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Gene: MED8 ENSGALG00010021429

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Description

mediator complex subunit 8 [Source:NCBI gene (formerly Entrezgene);Acc:424565]

Location

Primary_assembly 8: 19,395,904-19,405,964 reverse strand.

bGalGal1.mat.broiler.GRCg7b:CM028489.1

About this gene

This gene has 3 transcripts (splice variants) and 212 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSGALT00010051950.1	MED8-203	1350	275aa	ENSGALP00010031004.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V0ZI63	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,
ENSGALT00010051959.1	MED8-201	2466	267aa	ENSGALP00010031009.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V0ZI68	APPRIS ALT1: 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 is conserved in at least 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 ALT1,
ENSGALT00010051962.1	MED8-202	2222	268aa	ENSGALP00010031012.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1NG55	APPRIS P4: Where the APPRIS core modules are unable to choose a clear principal CDS and there is more than one variant with a distinct (but consecutive) CCDS identifiers, APPRIS selects the longest CCDS isoform as 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 P4,

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Summary

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