Human (GRCh38.p14)
Description

DiGeorge syndrome critical region gene 6 like [Source:HGNC Symbol;Acc:HGNC:18551]

Gene Synonyms

FLJ10666

Location

Chromosome 22: 20,314,238-20,320,080 reverse strand.

GRCh38:CM000684.2

About this gene

This gene has 10 transcripts (splice variants), 203 orthologues and 2 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000248879.8DGCR6L-2011172220aaENSP00000248879.2
 
Protein coding
CCDS13778Q9BY27 NM_033257.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P2TSL:1
ENST00000911281.1DGCR6L-2051138219aaENSP00000581340.1
 
Protein coding
--GENCODE PrimaryGENCODE BasicAPPRIS ALT2
ENST00000911283.1DGCR6L-2071104215aaENSP00000581342.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000911284.1DGCR6L-2081088210aaENSP00000581343.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000911286.1DGCR6L-2101061208aaENSP00000581345.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000875445.1DGCR6L-2041033201aaENSP00000545504.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000911282.1DGCR6L-2061018183aaENSP00000581341.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000405465.3DGCR6L-202962182aaENSP00000386052.3
 
Protein coding
B5MCQ4 -GENCODE PrimaryGENCODE BasicTSL:3
ENST00000911285.1DGCR6L-209913158aaENSP00000581344.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000443409.1DGCR6L-20393597aaENSP00000403341.1
 
Nonsense mediated decay
F8WCX1 -TSL:1