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: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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Pathway
Molecular interactions
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Gene: Med26 ENSRNOG00000012270

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Description

mediator complex subunit 26 [Source:RGD Symbol;Acc:1309524]

Gene Synonyms

LOC306328, Slc35e1

Location

Primary_assembly 16: 17,327,734-17,383,603 forward strand.

GRCr8:CM070406.1

About this gene

This gene has 4 transcripts (splice variants) and 260 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000146426.1	Med26-203	3737	651aa	ENSRNOP00000109189.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000121997.1	Med26-202	3882	539aa	ENSRNOP00000111891.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000158731.1	Med26-204	3518	578aa	ENSRNOP00000101524.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000085462.3	Med26-201	3006	540aa	ENSRNOP00000069747.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JW54	APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1,

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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues (Not available)

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data