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

Configure this page

Share this page

Bookmark this page

.

Gene: Pabpn1l ENSRNOG00000029558

.

Description

PABPN1 like [Source:RGD Symbol;Acc:1562761]

Gene Synonyms

Epabp2, LOC307920, Pabpnl1, RGD1562761

Location

Primary_assembly 19: 67,578,496-67,581,895 reverse strand.

GRCr8:CM070409.1

About this gene

This gene has 1 transcript (splice variant), 181 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000045052.6	Pabpn1l-201	1131	284aa	ENSRNOP00000050572.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QPA4 A6IZT6	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,

.

Summary

.

.