Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
- Paralogues
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ID History
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Gene: SRSF2 ENSGALG00000017357

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Description

serine and arginine rich splicing factor 2 [Source:NCBI gene;Acc:396195]

Gene Synonyms

SC-35, SFRS2

Location

Chromosome 18: 4,241,336-4,245,766 forward strand.

GRCg6a:CM000110.5

About this gene

This gene has 3 transcripts (splice variants), 367 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Name	Transcript ID	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
SRSF2-202	ENSGALT00000073781.2	3037	221aa	ENSGALP00000056912.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	P30352	<p>APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS.</p><p>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.</p>APPRIS P1,
SRSF2-201	ENSGALT00000028041.5	2357	221aa	ENSGALP00000027988.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A1I7Q430 P30352	<p>APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS.</p><p>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.</p>APPRIS P1,
SRSF2-203	ENSGALT00000107499.1	1842	221aa	ENSGALP00000071757.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	P30352	<p>APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS.</p><p>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.</p>APPRIS P1,

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Summary

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Gene-based displays