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Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Paralogues
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
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: FBXO39 ENSG00000177294

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Description

F-box protein 39 [Source:HGNC Symbol;Acc:28565]

Gene Synonyms

FBX39, Fbx39, MGC35179

Location

Chromosome 17: 6,679,542-6,700,420 forward strand.

GRCh37:CM000679.1

About this gene

This gene has 3 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000321535.4	FBXO39-001	1677	442aa	ENSP00000321386.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS11082	Q8N4B4	NM_153230.2	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,
ENST00000575022.1	FBXO39-003	1268	36aa	ENSP00000458890.1	Nonsense mediated decay		I3L1J5	-	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENST00000572251.1	FBXO39-002	917	50aa	ENSP00000459284.1	Nonsense mediated decay		-	-	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,

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Summary

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