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: Prdm8 ENSRNOG00000002004

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Description

PR/SET domain 8 [Source:RGD Symbol;Acc:1311628]

Gene Synonyms

LOC305198

Location

Primary_assembly 14: 11,404,407-11,410,993 reverse strand.

mRatBN7.2:CM026987.1

About this gene

This gene has 1 transcript (splice variant), 194 orthologues, 1 paralogue and is associated with 4 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000002746.7	Prdm8-201	3083	689aa	ENSRNOP00000002746.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4A123	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,

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Summary

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