Human (GRCh38.p14)
Description

F-box and WD repeat domain containing 2 [Source:HGNC Symbol;Acc:HGNC:13608]

Gene Synonyms

FBW2, FWD2, MD6

About this transcript

This transcript has 8 exons, is annotated with 28 domains and features, is associated with 15133 variant alleles and maps to 732 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000608872.6FBXW2-2039142454aaENSP00000476369.1
 
Protein coding
CCDS43872Q9UKT8-1 NM_012164.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000684001.2FBXW2-2048622454aaENSP00000507010.1
 
Protein coding
CCDS43872Q9UKT8-1 -GENCODE PrimaryGENCODE BasicAPPRIS P1
ENST00000684047.2FBXW2-2058443454aaENSP00000508157.1
 
Protein coding
CCDS43872Q9UKT8-1 -GENCODE PrimaryGENCODE BasicAPPRIS P1
ENST00000684405.2FBXW2-2068270325aaENSP00000508243.1
 
Protein coding
CCDS94471B4DT60 -GENCODE PrimaryGENCODE Basic
ENST00000453291.2FBXW2-2013560187aaENSP00000398662.2
 
Nonsense mediated decay
Q4VXH1 -TSL:5
ENST00000493559.1FBXW2-2022154No protein-
 
Protein coding CDS not defined
--TSL:2
Statistics

Exons: 8, Coding exons: 6, Transcript length: 8,622 bps, Translation length: 454 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9UKT8

CCDS

This transcript is a member of the Human CCDS set: CCDS43872

Version

ENST00000684001.2

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.

GENCODE primary gene

This transcript is a member of the Gencode Primary gene set.