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Human (GRCh38.p14)
Description

insulin induced gene 2 [Source:HGNC Symbol;Acc:HGNC:20452]

Location

Chromosome 2: 118,088,452-118,110,997 forward strand.

GRCh38:CM000664.2

About this gene

This gene has 7 transcripts (splice variants), 206 orthologues and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000245787.9INSIG2-2013562225aaENSP00000245787.4
 
Protein coding
CCDS2122Q9Y5U4 NM_016133.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000411929.5INSIG2-20257439aaENSP00000400126.1
 
Nonsense mediated decay
F8WCG8 -TSL:2
ENST00000485520.5INSIG2-2063185No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000471186.5INSIG2-2042100No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000467223.5INSIG2-203627No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000479999.1INSIG2-205532No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000488995.1INSIG2-207518No protein-
 
Protein coding CDS not defined
--TSL:3