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FLG and neurodevelopmental disorder are reported together in 1 article.

Gene

FLG

HGNC
HGNC:3748
12articles
12mentions
2variants with confirmed gene link
Most co-reported phenotypes (articles)
Reported variants (articles · ClinVar status)
HPO
HP:0012759
450articles
450mentions
12co-reported genes shown
Most co-reported genes (articles)

Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.

Publications

1 records shown · first 60

Clinical and genetic characterization of patients segregating variants in KPTN, MINPP1, NGLY1, AP4B1, and SON underlying neurodevelopmental disorders: Genetic and phenotypic expansion.

PMID 36181241 | DOI 10.1002/jdn.10231 · International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience · 2022 · 19 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneFLG“Interestingly, additional heterozygous nonsense variant in SON: NM_138927.2: c.5753_5756del: NP_620305.3; p.(Val1918GlufsTer87) and a homozygous variant in FLG (FLG: NM_002016.2:c.7339C>T: NP_002007.1; p.(Arg2447X) were detected in families A and D, respectively.”0.98hgnc_dict_v1
phenotypeneurodevelopmental disorder“Clinical and genetic characterization of patients segregating variants in KPTN, MINPP1, NGLY1, AP4B1, and SON underlying neurodevelopmental disorders: Genetic and phenotypic expansion.”0.93phenotype_alias_lexicon_v2
geneKPTN“Clinical and genetic characterization of patients segregating variants in KPTN, MINPP1, NGLY1, AP4B1, and SON underlying neurodevelopmental disorders: Genetic and phenotypic expansion.”0.98hgnc_dict_v1
geneMINPP1“Clinical and genetic characterization of patients segregating variants in KPTN, MINPP1, NGLY1, AP4B1, and SON underlying neurodevelopmental disorders: Genetic and phenotypic expansion.”0.98hgnc_dict_v1