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: srsf1b ENSDARG00000017843

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Description

serine and arginine rich splicing factor 1b [Source:NCBI gene;Acc:393565]

Gene Synonyms

sfrs1, sfrs1b, wu:fb80g05, zgc:111894, zgc:65898, zgc:76897

Location

Chromosome 21: 39,567,505-39,577,517 reverse strand.

GRCz11:CM002905.2

About this gene

This gene has 1 transcript (splice variant), 179 orthologues and 14 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000143566.4	srsf1b-201	4032	245aa	ENSDARP00000116886.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q6NYA0	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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