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

Configure this page

Share this page

Bookmark this page

.

Gene: SF1 ENSSSCG00000062583

.

Description

splicing factor 1 [Source:HGNC Symbol;Acc:HGNC:12950]

Location

Primary_assembly 2: 7,391,383-7,404,948 forward strand.

Sscrofa11.1:CM000813.5

About this gene

This gene has 2 transcripts (splice variants), 185 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000046089.3	SF1-201	3493	763aa	ENSSSCP00000053679.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287BC34	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,
ENSSSCT00000062161.3	SF1-202	3124	639aa	ENSSSCP00000049141.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287AZ25 A0A4X1VAQ9	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,

.

Summary

.

.