Human (GRCh38.p14)
Description

DiGeorge syndrome critical region gene 6 [Source:HGNC Symbol;Acc:HGNC:2846]

Location

Chromosome 22: 18,906,028-18,914,238 forward strand.

GRCh38:CM000684.2

About this gene

This gene has 8 transcripts (splice variants), 205 orthologues, 2 paralogues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000331444.12DGCR6-2011117220aaENSP00000331681.6
 
Protein coding
CCDS13753Q14129-1 NM_005675.6MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000608842.1DGCR6-2081837144aaENSP00000476388.1
 
Protein coding
K7ELY4 -GENCODE basicTSL:2
ENST00000413981.5DGCR6-202103984aaENSP00000402409.1
 
Protein coding
Q6FGH4 -GENCODE basicTSL:1
ENST00000483718.5DGCR6-2073245104aaENSP00000467483.1
 
Nonsense mediated decay
K7EPQ2 -TSL:5
ENST00000480608.5DGCR6-2061435144aaENSP00000466276.1
 
Nonsense mediated decay
K7ELY4 -TSL:2
ENST00000427407.5DGCR6-2031199162aaENSP00000397633.2
 
Nonsense mediated decay
Q14129-2 -TSL:5
ENST00000436645.1DGCR6-204812No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000477156.1DGCR6-205524No protein-
 
Retained intron
--TSL:2