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  3. LFNG
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Spondylocostal Dysostosis

Gene: LFNG

Green List (high evidence)
LFNG (LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase)
EnsemblGeneIds (GRCh38): ENSG00000106003
EnsemblGeneIds (GRCh37): ENSG00000106003
OMIM: 602576, Gene2Phenotype
LFNG is in 6 panels

0 reviews

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Spondylocostal dysostosis 3, autosomal recessive MIM#609813
OMIM
602576
Clinvar variants
Variants in LFNG
Penetrance
None
Panels with this gene

History Filter Activity

16 Feb 2024, Gel status: 3

Set Phenotypes

Elena Savva (Victorian Clinical Genetics Services)

Phenotypes for gene: LFNG were changed from Spondylocostal dysostosis 3, autosomal recessive MIM#609813 to Spondylocostal dysostosis 3, autosomal recessive MIM#609813

16 Feb 2024, Gel status: 3

Set Phenotypes

Elena Savva (Victorian Clinical Genetics Services)

Phenotypes for gene: LFNG were changed from to Spondylocostal dysostosis 3, autosomal recessive MIM#609813

16 Feb 2024, Gel status: 3

Entity classified by Genomics England curator

Elena Savva (Victorian Clinical Genetics Services)

Gene: lfng has been classified as Green List (High Evidence).

17 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: LFNG was added gene: LFNG was added to Spondylocostal Dysostosis_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: LFNG was set to BIALLELIC, autosomal or pseudoautosomal