Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
Ontologies
- GO: Cellular component
- GO: Biological process
- GO: Molecular function
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Snord14e ENSMUSG00002076818

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Description

small nucleolar RNA, C/D box 14E [Source:MGI Symbol;Acc:MGI:3851606]

Location

Chromosome 9: 40,716,044-40,716,133 forward strand.

GRCm39:CM001002.3

About this gene

This gene has 1 transcript (splice variant), 70 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	Flags
ENSMUST00020181739.1	Snord14e-201	90	No protein	-	Small RNA molecules that are found in the cell nucleolus and are involved in the post-transcriptional modification of other RNAs.snoRNA		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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,

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Summary

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