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

Gene: Ugt2b ENSRNOG00000046540

Description

UDP glycosyltransferase 2 family, polypeptide B [Source:RGD Symbol;Acc:3936]

Gene Synonyms

LOC102550618, LOC102550717, LOC688226, LOC689702, RLUG23, Rlug38, UDPGT 2B17, UDPGT 2B2, UDPGT 2B3, UDPGT 2B5, UDPGTr-4, Udpgt, Udpgtr-3, Ugt2b17, Ugt2b2, Ugt2b3, Ugt2b5

Location

Primary_assembly 14: 20,817,285-20,833,917 forward strand.

mRatBN7.2:CM026987.1

About this gene

This gene has 1 transcript (splice variant), 430 orthologues and 14 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000047655.6	Ugt2b-201	1896	530aa	ENSRNOP00000045002.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1M7N8	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,

Gene: Ugt2b ENSRNOG00000046540

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Gene: Ugt2b ENSRNOG00000046540

Summary

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