Human (GRCh38.p14)
Description

SAM and SH3 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:19182]

Gene Synonyms

DJ323M4.1, KIAA0790, SH3D6A

Location

Chromosome 6: 148,272,304-148,552,044 forward strand.

GRCh38:CM000668.2

About this gene

This gene has 10 transcripts (splice variants), 269 orthologues, 2 paralogues and is associated with 4 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000367467.8SASH1-20174601247aaENSP00000356437.3
 
Protein coding
CCDS5212O94885 NM_015278.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000636279.1SASH1-2061077359aaENSP00000490865.1
 
Protein coding
A0A1B0GWB9 -TSL:5CDS 5' and 3' incomplete
ENST00000637729.1SASH1-210875161aaENSP00000490521.1
 
Protein coding
A0A1B0GVI0 -TSL:2CDS 3' incomplete
ENST00000637469.1SASH1-20852341aaENSP00000490499.1
 
Nonsense mediated decay
A0A1B0GVF9 -TSL:4CDS 5' incomplete
ENST00000635873.1SASH1-204579No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000637029.1SASH1-207571No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000637498.1SASH1-209552No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000470750.1SASH1-203617No protein-
 
Retained intron
--TSL:3
ENST00000367469.5SASH1-202591No protein-
 
Retained intron
--TSL:3
ENST00000635969.1SASH1-205489No protein-
 
Retained intron
--TSL:4