Human (GRCh38.p14)
Description

TSC22 domain family member 1 [Source:HGNC Symbol;Acc:HGNC:16826]

Gene Synonyms

MGC17597, TGFB1I4, TSC22

Location

Chromosome 13: 44,432,143-44,577,147 reverse strand.

GRCh38:CM000675.2

About this gene

This gene has 12 transcripts (splice variants), 183 orthologues and 3 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000458659.3TSC22D1-20359611073aaENSP00000397435.2
 
Protein coding
CCDS31966Q15714-1 NM_183422.4MANE SelectEnsembl CanonicalGENCODE basicTSL:1
ENST00000261489.7TSC22D1-2013148144aaENSP00000261489.2
 
Protein coding
CCDS9392Q15714-2 -GENCODE basicAPPRIS P1TSL:1
ENST00000611198.4TSC22D1-211287786aaENSP00000481585.1
 
Protein coding
CCDS73565A0A087X0H8 -GENCODE basicTSL:2
ENST00000622051.1TSC22D1-212287286aaENSP00000483407.1
 
Protein coding
CCDS73565A0A087X0H8 -GENCODE basicTSL:2
ENST00000493016.1TSC22D1-208690142aaENSP00000418739.1
 
Protein coding
C9IZ15 -TSL:4CDS 3' incomplete
ENST00000472477.1TSC22D1-20534941aaENSP00000419864.1
 
Protein coding
C9JYW3 -TSL:5CDS 3' incomplete
ENST00000486464.1TSC22D1-2061093149aaENSP00000417476.1
 
Nonsense mediated decay
H7C4J9 -TSL:5CDS 5' incomplete
ENST00000460842.5TSC22D1-204903No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000496314.1TSC22D1-209608No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000487881.2TSC22D1-207571No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000437455.2TSC22D1-202434No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000496838.1TSC22D1-210551No protein-
 
Retained intron
--TSL:1