Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
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Gene: Rpp30 ENSRNOG00000018718

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Description

ribonuclease P/MRP subunit p30 [Source:RGD Symbol;Acc:1595116]

Gene Synonyms

LOC685332, MGC187977

Location

Primary_assembly 1: 243,198,713-243,221,553 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 4 transcripts (splice variants) and 215 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000110649.2	Rpp30-204	1543	303aa	ENSRNOP00000091750.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AG83	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,
ENSRNOT00000107919.2	Rpp30-203	1520	280aa	ENSRNOP00000095685.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6APH8	-
ENSRNOT00000025412.6	Rpp30-201	1423	263aa	ENSRNOP00000025413.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZU51	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSRNOT00000097535.2	Rpp30-202	1408	258aa	ENSRNOP00000090910.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GJ86	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,

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Summary

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