Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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: SNRPG ENSPTRG00000012029

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Description

small nuclear ribonucleoprotein polypeptide G [Source:VGNC Symbol;Acc:VGNC:380]

Location

Chromosome 2A: 71,716,092-71,728,476 reverse strand.

Pan_tro_3.0:CM000315.3

About this gene

This gene has 3 transcripts (splice variants), 152 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000099047.1	SNRPG-203	291	96aa	ENSPTRP00000067380.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RST7 A0A6D2W7R9	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,
ENSPTRT00000097850.1	SNRPG-201	1265	64aa	ENSPTRP00000065460.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2J8N488 A0A6D2XT12	-
ENSPTRT00000022382.2	SNRPG-202	620	76aa	ENSPTRP00000020652.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2W8Y8 H2QI24	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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