Fraser syndrome 3

Summary
Synonym
  • FRASRS3
Definition
A Fraser syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the GRIP1 gene on chromosome 12q14.3.
Super Class
Fraser syndrome
Disease Ontology
DOID:0111406
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
23426 GRIP1 glutamate receptor interacting protein 1
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
Q9Y3R0 Glutamate receptor-interacting protein 1

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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: August 4, 2025