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
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: RNPS1 ENSSSCG00000008048

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Description

RNA binding protein with serine rich domain 1 [Source:VGNC Symbol;Acc:VGNC:92403]

Location

Primary_assembly 3: 39,739,308-39,750,005 forward strand.

Sscrofa11.1:CM000814.5

About this gene

This gene has 2 transcripts (splice variants) and 288 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000008820.5	RNPS1-202	2204	341aa	ENSSSCP00000008596.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D0RMH7 A0A8D1X1L3	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,
ENSSSCT00000047693.3	RNPS1-201	1637	211aa	ENSSSCP00000032442.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A286ZLK7 A0A4X1VV33	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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Orthologues

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