Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
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External references
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ID History
- Gene history

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Gene: PRPF8 ENSPTRG00000039576

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Description

pre-mRNA processing factor 8 [Source:VGNC Symbol;Acc:VGNC:51727]

Location

Chromosome 17: 1,647,805-1,693,627 reverse strand.

Pan_tro_3.0:CM000331.3

About this gene

This gene has 1 transcript (splice variant) and 214 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000074067.2	PRPF8-201	7324	2335aa	ENSPTRP00000060306.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XTX5 K7DMH6	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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