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

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Gene: SELENOM ENSSSCG00000029781

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Description

selenoprotein M [Source:NCBI gene (formerly Entrezgene);Acc:100302025]

Gene Synonyms

SELM

Location

Primary_assembly 14: 47,902,864-47,905,440 reverse strand.

Sscrofa11.1:CM000825.5

About this gene

This gene has 2 transcripts (splice variants), 179 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000098826.1	SELENOM-202	1283	151aa	ENSSSCP00000079641.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8W4FJJ8	-
ENSSSCT00000029493.4	SELENOM-201	703	142aa	ENSSSCP00000022697.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	C4PK53 I3LF57	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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