Human (GRCh38.p14) ▼
Description

SH3 and PX domains 2B [Source:HGNC Symbol;Acc:HGNC:29242]

Gene Synonyms

FLJ20831, KIAA1295

Location

Chromosome 5: 172,323,171-172,454,536 reverse strand.

GRCh38:CM000667.2

About this gene

This gene has 13 transcripts (splice variants), 204 orthologues, 3 paralogues and is associated with 4 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000311601.6SH3PXD2B-2017779911aaENSP00000309714.5
 
Protein coding
CCDS34291A1X283 NM_001017995.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00001134615.1SH3PXD2B-2137785911aaENSP00000806078.1
 
Protein coding
CCDS34291--Ensembl Canonical ExtendedGENCODE BasicAPPRIS P1
ENST00000918640.1SH3PXD2B-2067887945aaENSP00000588699.1
 
Protein coding
--GENCODE Basic
ENST00000918641.1SH3PXD2B-2077711895aaENSP00000588700.1
 
Protein coding
--GENCODE Basic
ENST00000971124.2SH3PXD2B-2085170939aaENSP00000641183.1
 
Protein coding
--GENCODE Basic
ENST00000519643.6SH3PXD2B-2033577430aaENSP00000430890.1
 
Protein coding
CCDS78084G3V144 -GENCODE BasicTSL:1
ENST00001106233.1SH3PXD2B-2112695339aaENSP00000776038.1
 
Protein coding
--GENCODE Basic
ENST00001006966.1SH3PXD2B-2092391134aaENSP00000676783.1
 
Protein coding
--GENCODE Basic
ENST00001112080.1SH3PXD2B-2122138409aaENSP00000781885.1
 
Protein coding
--GENCODE Basic
ENST00000636523.1SH3PXD2B-2051609444aaENSP00000490082.1
 
Protein coding
A0A1B0GUF2 -TSL:5CDS 5' incomplete
ENST00000518522.5SH3PXD2B-20247181aaENSP00000428076.1
 
Protein coding
H0YAU1 -TSL:5CDS 5' incomplete
ENST00001087809.1SH3PXD2B-210771389aaENSP00000757615.1
 
Nonsense mediated decay
---
ENST00000523651.1SH3PXD2B-204390No protein-
 
Protein coding CDS not defined
--TSL:3