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Gene : INS-IGF2 Homo sapiens

Name  ? INS-IGF2 readthrough Cytological Location  11p15.5
Brief Description  INS-IGF2 readthrough
Description  This locus includes two alternatively spliced read-through transcript variants which align to the INS gene in the 5' region and to the IGF2 gene in the 3' region. One transcript is predicted to encode a protein which shares the N-terminus with the INS protein but has a distinct and longer C-terminus, whereas the other transcript is a candidate for nonsense-mediated decay (NMD). The transcripts are imprinted and are paternally expressed in the limb and eye. [provided by RefSeq, Jul 2008]
  • synonyms:
  • HGNC:33527,
  • DQ104205,
  • INS-IGF2,
  • NM_001042376.2,
  • OTTHUMG00000166213,
  • uc001lvm.4
  • identifiers:
  • 723961,
  • ENSG00000129965,
  • INS-IGF2

Genome feature

Region: gene ? Length: 32093  
Location: 11:2129117-2161209 reverse strand Cyto location: 11p15.5

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

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Gene --> Proteins.


Gene Report --> GWAS hit


0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



0 Pathways

0 SN Ps

4 Cross References

12 Data Sets

1 Homologues

0 Located Features

140 Rna Seq Results