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

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Gene: LMNB2 ENSPTRG00000010238

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Description

lamin B2 [Source:VGNC Symbol;Acc:VGNC:2322]

Location

Chromosome 19: 2,496,148-2,524,913 reverse strand.

Pan_tro_3.0:CM000333.3

About this gene

This gene has 3 transcripts (splice variants), 190 orthologues and 80 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000018803.4	LMNB2-202	4666	620aa	ENSPTRP00000017403.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XN58 H2QEX0	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,
ENSPTRT00000097985.1	LMNB2-201	4275	483aa	ENSPTRP00000086301.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3TAK9	-
ENSPTRT00000078334.1	LMNB2-203	1815	604aa	ENSPTRP00000086514.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3TBB1	-

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Summary

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