Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
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: Snrnp27 ENSRNOG00000017838

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Description

small nuclear ribonucleoprotein U4/U6.U5 subunit 27 [Source:RGD Symbol;Acc:1310925]

Gene Synonyms

LOC362392, RGD1310925, Ry1

Location

Primary_assembly 4: 120,697,976-120,737,257 reverse strand.

GRCr8:CM070394.1

About this gene

This gene has 3 transcripts (splice variants), 226 orthologues and 5 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000024414.7	Snrnp27-201	2947	524aa	ENSRNOP00000024414.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6IAZ0 F7ERJ6	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,
ENSRNOT00000118148.2	Snrnp27-203	2881	502aa	ENSRNOP00000095491.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6B2P7	-
ENSRNOT00000104724.2	Snrnp27-202	810	199aa	ENSRNOP00000095104.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AN78	-

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Summary

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