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
External references
Supporting evidence
ID History
- Gene history

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Gene: Stpg2 ENSRNOG00000023457

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Description

sperm-tail PG-rich repeat containing 2 [Source:RGD Symbol;Acc:1591946]

Gene Synonyms

LOC499719

Location

Primary_assembly 2: 230,437,681-230,959,218 forward strand.

GRCr8:CM070392.1

About this gene

This gene has 2 transcripts (splice variants), 144 orthologues and 5 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000029382.6	Stpg2-201	2375	572aa	ENSRNOP00000031925.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A1A5R9	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,
ENSRNOT00000094402.2	Stpg2-202	2378	563aa	ENSRNOP00000081550.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A1A5R9	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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