Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Prdm15 ENSRNOG00000001620

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Description

PR/SET domain 15 [Source:RGD Symbol;Acc:1310055]

Gene Synonyms

LOC304054

Location

Primary_assembly 11: 37,165,575-37,222,207 reverse strand.

mRatBN7.2:CM026984.1

About this gene

This gene has 2 transcripts (splice variants), 209 orthologues, 17 paralogues and is associated with 7 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000046318.6	Prdm15-201	5176	1148aa	ENSRNOP00000041592.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZQ99	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 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,
ENSRNOT00000114092.1	Prdm15-202	5059	1109aa	ENSRNOP00000084210.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZYR1	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,

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Summary

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