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IGFALS

IGFALS
Identifiers
Aliases IGFALS, ALS, ACLSD, insulin like growth factor binding protein acid labile subunit
External IDs MGI: 107973 HomoloGene: 37987 GeneCards: IGFALS
Gene location (Human)
Chromosome 16 (human)
Chr. Chromosome 16 (human)
Chromosome 16 (human)
Genomic location for IGFALS
Genomic location for IGFALS
Band 16p13.3 Start 1,790,413 bp
End 1,794,971 bp
RNA expression pattern
PBB GE IGFALS 215712 s at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001146006
NM_004970

NM_008340

RefSeq (protein)

NP_001139478
NP_004961

NP_032366

Location (UCSC) Chr 16: 1.79 – 1.79 Mb Chr 16: 24.88 – 24.88 Mb
PubMed search

NM_001146006
NM_004970

NM_008340

NP_001139478
NP_004961

NP_032366

Insulin-like growth factor binding protein, acid labile subunit, also known as IGFALS, is a protein which in humans is encoded by the IGFALS gene.

The protein encoded by this gene is a serum protein that binds insulin-like growth factors, increasing their half-life and their vascular localization. Production of the encoded protein, which contains twenty leucine-rich repeats, is stimulated by growth hormone. Three transcript variants encoding two different isoforms have been found for this gene.

Defects in this gene are a cause of acid-labile subunit deficiency, which manifests itself in a delayed and slow puberty.

IGFALS has been shown to interact with IGFBP3.


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