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

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Gene: PRPF4 ENSPTRG00000021274

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Description

pre-mRNA splicing tri-snRNP complex factor PRPF4 [Source:VGNC Symbol;Acc:VGNC:4830]

Location

Chromosome 9: 91,232,522-91,250,724 forward strand.

Pan_tro_3.0:CM000323.3

About this gene

This gene has 2 transcripts (splice variants) and 206 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000082975.1	PRPF4-202	1620	539aa	ENSPTRP00000062395.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RCN1	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,
ENSPTRT00000039327.4	PRPF4-201	3904	522aa	ENSPTRP00000036338.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2X506 H2QXQ4	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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