Variant ID | 26504 |
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Entrez Gene ID | 3486 |
Gene | IGFBP3 (GeneCards) |
Location | hg19 7:46312834-46312834
hg38 7:46273236-46273236 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000007.13:g.46312834 A>C (Genome Assembly: GRCh37) |
Exon or Intron | NA |
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Position in protein | NA |
Amino acid changes in protein | NA > NA |
Position in cDNA | NA |
Changes in cDNA | NA > NA |
mRNA accession | NA |
mRNA length | NA |
Reference length | 159138663 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.2202 |
CADD Raw score (version 1.3) | -0.262318 (Deleterious) |
FATHMM raw prediction score | 0.0793 (Tolerated) |
Deleterious probability by DeFine | 0.3401 (Neutral) |
Entrez Gene ID | 3486 (NCBI Gene) |
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Official Gene Symbol | IGFBP3 (GeneCards) |
Number of variants in IGFBP3 in this database | 29 (view all the variants) |
Full name | insulin like growth factor binding protein 3 |
Band | 7p12.3 |
Other IDs | Vega: OTTHUMG00000023769 OMIM: 146732 HGNC: HGNC:5472 Ensembl: ENSG00000146674 |
Other names | IBP3, BP-53 |
Summary | This gene is a member of the insulin-like growth factor binding protein (IGFBP) family and encodes a protein with an IGFBP domain and a thyroglobulin type-I domain. The protein forms a ternary complex with insulin-like growth factor acid-labile subunit (IGFALS) and either insulin-like growth factor (IGF) I or II. In this form, it circulates in the plasma, prolonging the half-life of IGFs and altering their interaction with cell surface receptors. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008] |
Individual ID | 29217587.03 (view all the variants in this individual) |
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Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |