Human (GRCh37.p13)
Description

DiGeorge syndrome critical region gene 2 [Source:HGNC Symbol;Acc:2845]

Gene Synonyms

DGS-C, IDD, KIAA0163, LAN, SEZ-12

Location
About this transcript

This transcript has 10 exons, is annotated with 21 domains and features, is associated with 26872 variant alleles and maps to 682 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000545799.1DGCR2-2024812269aaENSP00000445069.1
 
Protein coding
Q5CZ70 -GENCODE basic
ENST00000263196.7DGCR2-0014480550aaENSP00000263196.7
 
Protein coding
CCDS33598B7Z3C4 B7Z8B7 P98153
NM_005137.2GENCODE basic
ENST00000537045.1DGCR2-2014361509aaENSP00000440062.1
 
Protein coding
CCDS54496B7Z3C4 P98153 NM_001173534.1GENCODE basic
ENST00000389262.4DGCR2-0024814326aaENSP00000373914.4
 
Nonsense mediated decay
B7Z3C4 --
ENST00000473832.1DGCR2-004606No protein-
 
Processed transcript
---
ENST00000608548.1DGCR2-005518No protein-
 
Processed transcript
---
ENST00000467659.1DGCR2-0032459No protein-
 
Retained intron
---
Statistics

Exons: 10, Coding exons: 10, Transcript length: 4,480 bps, Translation length: 550 residues

CCDS

This transcript is a member of the Human CCDS set: CCDS33598

Uniprot

This transcript corresponds to the following Uniprot identifiers: P98153

Version

ENST00000263196.7

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Transcript having exact match between ENSEMBL and HAVANA:
OTTHUMT00000316504 (version 1)
GENCODE basic gene

This transcript is a member of the Gencode basic gene set.