Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: SELENOM ENSBTAG00000031279

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Description

selenoprotein M [Source:VGNC Symbol;Acc:VGNC:53920]

Location

Primary_assembly 17: 69,961,541-69,964,345 reverse strand.

ARS-UCD2.0:CM008184.2

About this gene

This gene has 2 transcripts (splice variants), 178 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000044309.6	SELENOM-201	625	143aa	ENSBTAP00000041817.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BKK9	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,
ENSBTAT00000141272.1	SELENOM-202	715	141aa	ENSBTAP00000104850.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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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Summary

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