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Neurofibromin 1 MeSH Descriptor Data 2022


MeSH Heading
Neurofibromin 1
Tree Number(s)
D12.644.360.325.150.500.460
D12.776.476.325.150.500.460
D12.776.624.776.610
Unique ID
D025542
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D025542
Scope Note
A protein found most abundantly in the nervous system. Defects or deficiencies in this protein are associated with NEUROFIBROMATOSIS 1, Watson syndrome, and LEOPARD syndrome. Mutations in the gene (GENE, NEUROFIBROMATOSIS 1) affect two known functions: regulation of ras-GTPase and tumor suppression.
Entry Term(s)
NF-1 Protein
NF1 GRP
NF1 Protein
NF1-GAP-Related Protein
Neurofibromatosis Type 1 Gene Product
Neurofibromatosis Type 1 Protein
Neurofibromin
Registry Number
0
Previous Indexing
Nerve Tissue Proteins (1995-2001)
Proteins (1990-1999)
See Also
Genes, Neurofibromatosis 1
Neurofibromatosis 1
Public MeSH Note
2002
History Note
2002
Date Established
2002/01/01
Date of Entry
2001/07/25
Revision Date
2015/11/24
Neurofibromin 1 Preferred
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