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

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Gene: LSM8 ENSBTAG00000012649

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Description

LSM8 homolog, U6 small nuclear RNA associated [Source:VGNC Symbol;Acc:VGNC:31060]

Location

Primary_assembly 4: 82,786,232-82,805,846 forward strand.

ARS-UCD1.3:CM008171.2

About this gene

This gene has 2 transcripts (splice variants), 207 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000102170.1	LSM8-202	408	102aa	ENSBTAP00000086070.1	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,
ENSBTAT00000016780.4	LSM8-201	703	94aa	ENSBTAP00000016780.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q3ZCE0	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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