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: Golga7 ENSRNOG00000017956

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Description

golgin A7 [Source:RGD Symbol;Acc:1359725]

Gene Synonyms

MGC93825

Location

Primary_assembly 16: 75,469,838-75,485,069 forward strand.

GRCr8:CM070406.1

About this gene

This gene has 4 transcripts (splice variants), 211 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000161872.1	Golga7-203	839	198aa	ENSRNOP00000104316.1	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,
ENSRNOT00000168169.1	Golga7-204	2076	163aa	ENSRNOP00000112237.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000096293.2	Golga7-202	1959	134aa	ENSRNOP00000077876.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5Y7Z1	-
ENSRNOT00000030960.5	Golga7-201	1942	152aa	ENSRNOP00000033324.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QIB4	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