Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
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  - Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
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Gene: Golga6l9 ENSRNOG00000031449

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Description

golgin A6 family like 9 [Source:RGD Symbol;Acc:1306441]

Gene Synonyms

LOC290425, RGD1306441, Spertl

Location

Primary_assembly 15: 78,875,241-78,876,736 forward strand.

GRCr8:CM070405.1

About this gene

This gene has 1 transcript (splice variant) and 17 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000043065.5	Golga6l9-201	1134	274aa	ENSRNOP00000048873.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HU42 D4ADT0	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,

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Summary

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