Insulin-like growth factor-binding protein, acid-labile subunit

Preferred Label : Insulin-like growth factor-binding protein, acid-labile subunit;

Symbol : IGFALS;

CISMeF acronym : IGFALS;

Type : Gene;

Alternative titles and symbols : Igfbp, soluble; Acid-labile subunit; ALS;

Description : In vivo, insulin-like growth factors I (IGF1; 147440) and II (IGF2; 147470) are always complexed to one of a family of 6 IGF-binding proteins, IGFBP1 (146730), IGFBP2 (146731), IGFBP3 (146732), IGFBP4 (146733), IGFBP5 (146734), and IGFBP6 (146735). Until birth, binary;

Ensembl ID : ENSG00000099769;

Prefixed ID : *601489;

Details

Origin ID

601489;

UMLS CUI

C1456383;

Automatic exact mappings (from CISMeF team)
- ALS [MedDRA LLT]
- Amyotrophic Lateral Sclerosis [NCIt concept]
- Amyotrophic lateral sclerosis [MedDRA Preferred Term]
- Amyotrophic lateral sclerosis [ICD-11 Subcategory]
- Amyotrophic lateral sclerosis [ORDO Disease]
- Antilymphocyte Serum [NCIt concept]
- IGFALS wt Allele [NCIt concept]
- Insulin-Like Growth Factor-Binding Protein Complex Acid Labile Subunit [NCIt concept]
- SOD1 wt Allele [NCIt concept]
- amyotrophic lateral sclerosis [MeSH Descriptor]
- amyotrophic lateral sclerosis [DO Concept]
- amyotrophic lateral sclerosis [MedlinePlus Topic]
- insulin like growth factor binding protein acid labile subunit [ORDO Gene]
- surgical soap [Artificial nutrition thesaurus concept]
Currated CISMeF NLP mapping
- insulin like growth factor binding protein acid labile subunit [HGNC gene]
HGNC gene
- insulin like growth factor binding protein acid labile subunit [HGNC gene]
Matching ORDO disease(s)
- Short stature due to primary acid-labile subunit deficiency [ORDO Disease]
NCIt concept(s)
- IGFALS Gene [NCIt concept]
- IGFALS wt Allele [NCIt concept]
- Insulin-Like Growth Factor-Binding Protein Complex Acid Labile Subunit [NCIt concept]
ORDO concept(s)
- insulin like growth factor binding protein acid labile subunit [ORDO Gene]
Phenotypes related
- Acid-labile subunit deficiency [OMIM Phenotype]
See also inter- (CISMeF)
- Acid Labile Subunit Measurement [NCIt concept]
- Growth hormone insensitivity syndrome [ORDO Disease]
- Short stature due to primary acid labile subunit deficiency (disorder) [SNOMED CT concept]
- Short stature due to primary acid-labile subunit deficiency [ORDO Disease]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- IGFALS Gene [NCIt concept]
- insulin like growth factor binding protein acid labile subunit [HGNC gene]

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