Summary
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: GOLGA8N ENSG00000283589

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Description

golgin A8 family member N [Source:HGNC Symbol;Acc:HGNC:44405]

Location

Scaffold HSCHR15_6_CTG8: 2,111,786-2,125,658 forward strand.

GRCh38:KQ031389.1

View this gene on the primary assembly.

About this gene

This gene has 2 transcripts (splice variants) and 1 gene allele.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000635923.2	GOLGA8N-209	5328	632aa	ENSP00000490331.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A1B0GV12	-	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000643824.1	GOLGA8N-210	5328	632aa	ENSP00000494486.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A1B0GV12	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,

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Summary

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