Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Cellular component
- GO: Molecular function
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: Vpreb1b ENSRNOG00000001839

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Description

V-set pre-B cell surrogate light chain 1B [Source:RGD Symbol;Acc:1564601]

Gene Synonyms

LOC100911573, LOC363830, RGD1564601, Vpreb1, Vpreb1_mapped, Vpreb2

Location

Primary_assembly 11: 97,629,102-97,632,051 forward strand.

GRCr8:CM070401.1

About this gene

This gene has 2 transcripts (splice variants), 101 orthologues and 254 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000134427.1	Vpreb1b-202	1101	242aa	ENSRNOP00000099432.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000081776.3	Vpreb1b-201	791	136aa	ENSRNOP00000074866.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6JSP4 D3Z922	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,

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Summary

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