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Gene : IGF2 Homo sapiens

Name  ? insulin like growth factor 2 Cytological Location  11p15.5
Brief Description  insulin like growth factor 2
Description  This gene encodes a member of the insulin family of polypeptide growth factors, which are involved in development and growth. It is an imprinted gene, expressed only from the paternal allele, and epigenetic changes at this locus are associated with Wilms tumour, Beckwith-Wiedemann syndrome, rhabdomyosarcoma, and Silver-Russell syndrome. A read-through INS-IGF2 gene exists, whose 5' region overlaps the INS gene and the 3' region overlaps this gene. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2010]
  • synonyms:
  • C11orf43,
  • NM_000612,
  • IGF2,
  • M29645,
  • preptin,
  • chromosome 11 open reading frame 43,
  • IGF-II,
  • insulin-like growth factor 2,
  • C11orf43,
  • GRDF,
  • OTTHUMG00000009395,
  • somatomedin A,
  • IGF-II,
  • uc001lvg.4,
  • AK025719,
  • PP9974,
  • HGNC:5466,
  • FLJ44734
  • identifiers:
  • 3481,
  • ENSG00000167244,
  • IGF2

Genome feature

Region: gene ? Length: 20492  
Location: 11:2129112-2149603 reverse strand Cyto location: 11p15.5


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Function

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Gene -> HPO annotation (Human Phenotype Ontology)

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Genomics

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Proteins

Gene --> Proteins.

SNPs

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Disease

4 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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Expression

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Other

90 SN Ps

5 Cross References

18 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results