Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: RSPRY1 ENSPTRG00000008149

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Description

ring finger and SPRY domain containing 1 [Source:VGNC Symbol;Acc:VGNC:9102]

Location

Chromosome 16: 47,883,880-47,918,017 forward strand.

Pan_tro_3.0:CM000330.3

About this gene

This gene has 2 transcripts (splice variants), 205 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000015028.5	RSPRY1-201	1881	576aa	ENSPTRP00000013916.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2W7W7 H2QB64	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,
ENSPTRT00000101939.1	RSPRY1-202	1584	527aa	ENSPTRP00000073782.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3S9R0	-

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Summary

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