Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: FBXW7 ENSBTAG00000007953

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Description

F-box and WD repeat domain containing 7 [Source:VGNC Symbol;Acc:VGNC:28926]

Location

Primary_assembly 17: 5,221,449-5,350,495 forward strand.

ARS-UCD1.3:CM008184.2

About this gene

This gene has 4 transcripts (splice variants), 210 orthologues and 15 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000086850.2	FBXW7-201	2401	707aa	ENSBTAP00000064414.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MNN4	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 ALT1: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that is conserved in at least three tested species. 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 ALT1,
ENSBTAT00000010457.7	FBXW7-204	2146	627aa	ENSBTAP00000010457.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A805E6P4	-
ENSBTAT00000109036.1	FBXW7-202	2055	640aa	ENSBTAP00000093380.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000071989.2	FBXW7-203	1832	589aa	ENSBTAP00000061665.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LW71	APPRIS P4: Where the APPRIS core modules are unable to choose a clear principal CDS and there is more than one variant with a distinct (but consecutive) CCDS identifiers, APPRIS selects the longest CCDS isoform as the principal variant. 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 P4,

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Breeds

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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