Varaico: Literature-Extracted Genetic Variants

Gene:FBP1
Variant:p.F194S
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FBP1

NM_000507.4:p.F194S

Associated Papers

A scalable approach to resolving variants of uncertain significance.

Tejura M et al.

Biorxiv : the Preprint Server for Biology, 2026

41727046 (PubMed )
Supplement: media-7.xlsx › VarChAMP_data_supp_mat_PP

Intrafamilial phenotypic variability due to a missense pathogenic variant in FBP1 gene.

Dalili S et al.

Molecular Genetics and Metabolism Reports, 2024

Fructose-1,6-bisphosphatase deficiency: estimation of prevalence in the Chinese population and analysis of genotype-phenotype association.

Ni Q et al.

Frontiers in Genetics, 2024

39036704 (PubMed )
Supplement: Table1.XLSX › Table_S1

Identification of genotype-biochemical phenotype correlations associated with fructose 1,6-bisphosphatase deficiency.

Sakuma I et al.

Communications Biology, 2023

Extensive disruption of protein interactions by genetic variants across the allele frequency spectrum in human populations.

Fragoza R et al.

Nature Communications, 2019

31515488 (PubMed )
Supplement: 41467_2019_11959_MOESM8_ESM.xlsx › SD4_-_HGMD_Mutations

Clinical and molecular characterization of Indian patients with fructose-1, 6-bisphosphatase deficiency: Identification of a frequent variant (E281K).

Bhai P et al.

Annals of Human Genetics, 2018

Functional variomics and network perturbation: connecting genotype to phenotype in cancer.

Yi S et al.

Nature Reviews. Genetics, 2017

A summary of molecular genetic findings in fructose-1,6-bisphosphatase deficiency with a focus on a common long-range deletion and the role of MLPA analysis.

Santer R et al.

Orphanet Journal of Rare Diseases, 2016

Human Metabolic Enzymes Deficiency: A Genetic Mutation Based Approach.

Chaturvedi S et al.

Scientifica, 2016

Two newly identified genomic mutations in a Japanese female patient with fructose-1,6-bisphosphatase (FBPase) deficiency.

Matsuura T et al.

Molecular Genetics and Metabolism, 2002

Novel fructose bisphosphatase 1 gene mutation presenting as recurrent episodes of vomiting in an Indian child.

Sharma AG et al.

Journal of Postgraduate Medicine, 0

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