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: SAMD13 ENSSSCG00000026005

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Description

sterile alpha motif domain containing 13 [Source:VGNC Symbol;Acc:VGNC:98609]

Location

Primary_assembly 6: 129,395,698-129,440,039 reverse strand.

Sscrofa11.1:CM000817.5

About this gene

This gene has 1 transcript (splice variant), 192 orthologues and 16 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000027176.4	SAMD13-201	1409	116aa	ENSSSCP00000023464.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D0LQR4 I3LHB9	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, 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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