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
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Gtf2b ENSRNOG00000011135

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Description

general transcription factor IIB [Source:RGD Symbol;Acc:619735]

Location

Primary_assembly 2: 234,427,637-234,446,049 forward strand.

GRCr8:CM070392.1

About this gene

This gene has 3 transcripts (splice variants), 218 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000089648.3	Gtf2b-202	1317	316aa	ENSRNOP00000070077.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JWZ8 A6HW74 P62916	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,
ENSRNOT00000119389.2	Gtf2b-203	1387	310aa	ENSRNOP00000093700.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AXE6	-
ENSRNOT00000015032.7	Gtf2b-201	1199	310aa	ENSRNOP00000015033.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0A0MXW7	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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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data