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: SAMSN1 ENSBTAG00000002623

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Description

SAM domain, SH3 domain and nuclear localization signals 1 [Source:VGNC Symbol;Acc:VGNC:34279]

Location

Primary_assembly 1: 22,510,546-22,675,631 forward strand.

ARS-UCD2.0:CM008168.2

About this gene

This gene has 3 transcripts (splice variants), 267 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000130605.2	SAMSN1-201	2629	656aa	ENSBTAP00000086776.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SN75	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,
ENSBTAT00000003394.6	SAMSN1-202	1786	366aa	ENSBTAP00000003394.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q3ZBW8	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,
ENSBTAT00000090896.2	SAMSN1-203	1196	198aa	ENSBTAP00000083631.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SI97	-

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Summary

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