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: Golga7b ENSRNOG00000015051

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Description

golgin A7 family, member B [Source:RGD Symbol;Acc:1583839]

Gene Synonyms

LOC309378

Location

Primary_assembly 1: 251,008,417-251,030,371 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants), 268 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000140540.1	Golga7b-202	3292	331aa	ENSRNOP00000099963.1	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,
ENSRNOT00000020390.9	Golga7b-201	3088	167aa	ENSRNOP00000020390.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6JHB2 F1M362	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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