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: Plxnb2 ENSRNOG00000007133

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Description

plexin B2 [Source:RGD Symbol;Acc:1305495]

Gene Synonyms

LOC315217

Location

Primary_assembly 7: 122,111,917-122,127,746 reverse strand.

GRCr8:CM070397.1

About this gene

This gene has 2 transcripts (splice variants), 318 orthologues, 8 paralogues and is associated with 6 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000088623.3	Plxnb2-202	6370	1841aa	ENSRNOP00000072434.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K2Y9 A6K7K6	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,
ENSRNOT00000010467.8	Plxnb2-201	6307	1820aa	ENSRNOP00000010467.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZQ57	-

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Summary

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