- Concept UI
- M0179586
- Registry Numbers
- 0
- 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.
- Terms
-
Neurofibromin 1
Preferred Term
Term UI
T431481
Date12/20/2000
LexicalTag
NON
ThesaurusID
NLM (2002)
-
NF-1 Protein
Term UI
T209585
Date01/01/1955
LexicalTag
ACX
ThesaurusID
NLM (2002)
-
NF1 GRP
Term UI
T209586
Date01/01/1955
LexicalTag
ACX
ThesaurusID
NLM (2002)
-
NF1 Protein
Term UI
T209587
Date01/01/1955
LexicalTag
ACX
ThesaurusID
NLM (2002)
-
Neurofibromatosis Type 1 Gene Product
Term UI
T209589
Date01/01/1955
LexicalTag
NON
ThesaurusID
NLM (2002)
-
Neurofibromin
Term UI
T209590
Date01/01/1955
LexicalTag
NON
ThesaurusID
NLM (2002)
-
Neurofibromatosis Type 1 Protein
Term UI
T209591
Date01/01/1955
LexicalTag
NON
ThesaurusID
NLM (2002)
-
NF1-GAP-Related Protein
Term UI
T209588
Date01/01/1955
LexicalTag
ACX
ThesaurusID
NLM (2002)