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

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Gene: PRPF19P1 ENSG00000264685

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Description

PRPF19 pseudogene 1 [Source:HGNC Symbol;Acc:23182]

Gene Synonyms

HsT1682, PRP19P, PRPF19P

Location

Chromosome 18: 63,735,986-63,736,883 reverse strand.

GRCh37:CM000680.1

About this gene

This gene has 1 transcript (splice variant).

Transcripts

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Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	RefSeq	Flags
ENST00000584766.1	PRPF19P1-001	898	No protein	-	Pseudogene that lack introns and is thought to arise from reverse transcription of mRNA followed by reinsertion of DNA into the genome.Processed pseudogene		-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,

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Summary

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