Human (GRCh38.p14)
Description

WT1 interacting protein [Source:HGNC Symbol;Acc:HGNC:20964]

Location
About this transcript

This transcript has 8 exons, is annotated with 35 domains and features, is associated with 15401 variant alleles and maps to 462 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000590071.7WTIP-20213545430aaENSP00000466953.2
 
Protein coding
CCDS59375A6NIX2 NM_001080436.2MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000954266.1WTIP-2052432409aaENSP00000624325.1
 
Protein coding
--GENCODE Basic
ENST00000924107.1WTIP-2032424407aaENSP00000594166.1
 
Protein coding
--GENCODE Basic
ENST00000954267.1WTIP-2062336396aaENSP00000624326.1
 
Protein coding
--GENCODE Basic
ENST00000924109.1WTIP-2042236418aaENSP00000594168.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000585928.1WTIP-201667200aaENSP00000465683.1
 
Protein coding
K7EKM1 -TSL:3CDS 5' incomplete
Statistics

Exons: 8, Coding exons: 8, Transcript length: 13,545 bps, Translation length: 430 residues

MANE

This MANE Select transcript contains ENSP00000466953 and matches to NM_001080436.2 and NP_001073905.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: A6NIX2

CCDS

This transcript is a member of the Human CCDS set: CCDS59375

Transcript Support Level (TSL)

TSL:1

Version

ENST00000590071.7

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

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.