Human (GRCh38.p14)
Description

SH2 domain containing 1A [Source:HGNC Symbol;Acc:HGNC:10820]

Gene Synonyms

DSHP, EBVS, IMD5, LYP, MTCP1, SAP, XLP, XLPD

Location

Chromosome X: 124,227,868-124,373,197 forward strand.

GRCh38:CM000685.2

About this gene

This gene has 16 transcripts (splice variants), 212 orthologues, 13 paralogues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000371139.9SH2D1A-2022236128aaENSP00000360181.5
 
Protein coding
CCDS14608O60880-1 NM_002351.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P3TSL:1
ENST00000698113.1SH2D1A-2093840128aaENSP00000513571.1
 
Protein coding
CCDS14608O60880-1 -GENCODE basicAPPRIS P3
ENST00000698116.1SH2D1A-2122276128aaENSP00000513572.1
 
Protein coding
CCDS14608O60880-1 -GENCODE basicAPPRIS P3
ENST00000360027.5SH2D1A-2012059125aaENSP00000353126.4
 
Protein coding
CCDS48162O60880-4 -GENCODE basicAPPRIS ALT1TSL:1
ENST00000698118.1SH2D1A-2141163128aaENSP00000513574.1
 
Protein coding
CCDS14608O60880-1 -GENCODE basicAPPRIS P3
ENST00000477673.2SH2D1A-20346176aaENSP00000477094.1
 
Protein coding
O60880-5 -GENCODE basicTSL:2
ENST00000494073.5SH2D1A-20541962aaENSP00000513589.1
 
Protein coding
O60880-6 -GENCODE basicTSL:1
ENST00000647259.2SH2D1A-207247177aaENSP00000494582.1
 
Nonsense mediated decay
A0A2R8Y573 --
ENST00000698117.1SH2D1A-213220276aaENSP00000513573.1
 
Nonsense mediated decay
A0A8V8TLH8 --
ENST00000491950.5SH2D1A-20447458aaENSP00000513588.1
 
Nonsense mediated decay
O60880-3 -TSL:2
ENST00000635645.1SH2D1A-2062554No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000698112.1SH2D1A-2082147No protein-
 
Protein coding CDS not defined
---
ENST00000698115.1SH2D1A-2112083No protein-
 
Protein coding CDS not defined
---
ENST00000698120.1SH2D1A-2161984No protein-
 
Protein coding CDS not defined
---
ENST00000698114.1SH2D1A-2101017No protein-
 
Protein coding CDS not defined
---
ENST00000698119.1SH2D1A-2152446No protein-
 
Retained intron
---