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Human (GRCh38.p14)
Description

WBP2 N-terminal like [Source:HGNC Symbol;Acc:HGNC:28389]

Gene Synonyms

FLJ26145, GRAMD7, MGC26816, PAWP

Location

Chromosome 22: 41,998,725-42,058,456 forward strand.

GRCh38:CM000684.2

About this gene

This gene has 10 transcripts (splice variants), 193 orthologues and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000328823.13WBP2NL-2012255309aaENSP00000332983.9
 
Protein coding
CCDS14029Q6ICG8 NM_152613.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000943073.1WBP2NL-2102368273aaENSP00000613132.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000329620.9WBP2NL-2023403309aaENSP00000328800.5
 
Nonsense mediated decay
CCDS14029Q6ICG8 -TSL:2
ENST00000412113.5WBP2NL-2031423273aaENSP00000389598.1
 
Nonsense mediated decay
F8WDR4 -TSL:5
ENST00000436265.5WBP2NL-2041417309aaENSP00000401002.1
 
Nonsense mediated decay
CCDS14029Q6ICG8 -TSL:2
ENST00000445185.1WBP2NL-20547583aaENSP00000400236.1
 
Nonsense mediated decay
F8WCF8 -TSL:3
ENST00000461730.1WBP2NL-2061309No protein-
 
Protein coding CDS not defined
--TSL:1
ENST00000475341.5WBP2NL-208569No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000487176.1WBP2NL-209431No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000470812.1WBP2NL-207579No protein-
 
Retained intron
--TSL:2