Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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: Lbr ENSRNOG00000052574

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Description

lamin B receptor [Source:RGD Symbol;Acc:620813]

Gene Synonyms

C14SR, Nbp60

Location

Primary_assembly 13: 96,071,081-96,095,709 reverse strand.

GRCr8:CM070403.1

About this gene

This gene has 2 transcripts (splice variants), 191 orthologues, 2 paralogues and is associated with 16 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000095219.2	Lbr-202	3551	621aa	ENSRNOP00000090637.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AEP6 A6JGK3	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,
ENSRNOT00000090712.3	Lbr-201	3473	595aa	ENSRNOP00000069002.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JU83	-

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Summary

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