Human (GRCh38.p14)
Description

SPT16 homolog, facilitates chromatin remodeling subunit [Source:HGNC Symbol;Acc:HGNC:11465]

Gene Synonyms

CDC68, FACT, FACTP140, FLJ10857, FLJ14010, SPT16/CDC68

Location

Chromosome 14: 21,351,476-21,384,019 reverse strand.

GRCh38:CM000676.2

About this gene

This gene has 8 transcripts (splice variants), 204 orthologues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000216297.7SUPT16H-20144331047aaENSP00000216297.2
 
Protein coding
CCDS9569Q9Y5B9 NM_007192.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000555943.1SUPT16H-20491583aaENSP00000450910.1
 
Protein coding
G3V2X0 -GENCODE basicTSL:2
ENST00000557652.1SUPT16H-20887781aaENSP00000451517.1
 
Nonsense mediated decay
G3V401 -TSL:5
ENST00000556309.5SUPT16H-20658266aaENSP00000452259.1
 
Nonsense mediated decay
G3V5A4 -TSL:3
ENST00000557394.5SUPT16H-2072324No protein-
 
Retained intron
--TSL:2
ENST00000556217.5SUPT16H-2051027No protein-
 
Retained intron
--TSL:2
ENST00000555752.1SUPT16H-203888No protein-
 
Retained intron
--TSL:2
ENST00000552829.2SUPT16H-202669No protein-
 
Retained intron
--TSL:2