Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: SPRTN ENSSSCG00000040087

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Description

SprT-like N-terminal domain [Source:NCBI gene (formerly Entrezgene);Acc:100155479]

Gene Synonyms

C14H1orf124

Location

Primary_assembly 14: 59,171,192-59,192,269 reverse strand.

Sscrofa11.1:CM000825.5

About this gene

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

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000049185.3	SPRTN-201	8650	483aa	ENSSSCP00000046574.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287ART8 A0A8D2CHD2	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,
ENSSSCT00000075452.2	SPRTN-202	1444	212aa	ENSSSCP00000061143.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2QSJ8	-

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Summary

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