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Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: INS-IGF2 ENSG00000129965

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Description

INS-IGF2 readthrough [Source:HGNC Symbol;Acc:33527]

Gene Synonyms

INSIGF

Location

Chromosome 11: 2,153,768-2,182,439 reverse strand.

GRCh37:CM000673.1

About this gene

This gene has 4 transcripts (splice variants) and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000397270.1	INS-IGF2-001	828	200aa	ENSP00000380440.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS41598	F8WCM5	NM_001042376.2	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000356578.4	INS-IGF2-002	1706	200aa	ENSP00000348986.4	Nonsense mediated decay	CCDS41598	F8WCM5	-	-
ENST00000481781.1	INS-IGF2-003	977	No protein	-	Gene/transcript that doesn't contain an open reading frame (ORF).Processed transcript		-	-	-
ENST00000476874.1	INS-IGF2-005	482	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-

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Summary

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