spondylocostal dysostosis 3

Summary
Synonym
  • SCDO3
  • autosomal recessive spondylocostal dysostosis 3
Definition
A spondylocostal dysostosis that has_material_basis_in homozygous or compound heterozygous mutation in the LFNG gene on chromosome 7p22.3.
Super Class
autosomal recessive disease spondylocostal dysostosis
Disease Ontology
DOID:0112361
Mondo Disease Ontology
OMIM
WikiPathways (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
3955 LFNG LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
Displaying 1 entry
Gene ID Gene Symbol Description Source
16848 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
Displaying 1 entry
Gene ID Gene Symbol Description Source
170905 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
Displaying 1 entry
Gene ID Gene Symbol Description Source
40314 fng fringe
Displaying 1 entry
Gene ID Gene Symbol Description Source
30158 lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
Displaying all 3 entries
Gene ID Gene Symbol Description Source Organism
397855 lfng.S LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase S homeolog Xenopus laevis (African clawed frog)
549805 lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase Xenopus tropicalis (tropical clawed frog)
100036937 lfng.L LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase L homeolog Xenopus laevis (African clawed frog)
Related Glycoprotein
The Human Phenotype Ontology
Displaying entries 31 - 40 of 44 in total
HPO ID HPO Term
HP:0000902 Rib fusion
HP:0010306 Short thorax
HP:0000269 Prominent occiput
HP:0003298 Spina bifida occulta
HP:0000069 Abnormality of the ureter
HP:0002093 Respiratory insufficiency
HP:0005108 Abnormal intervertebral disk morphology
HP:0000463 Anteverted nares
HP:0003577 Congenital onset
HP:0004598 Supernumerary vertebral ossification centers
Displaying 1 entry
Gene ID Gene Symbol Description
3955 LFNG LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024