NF1 - neurofibromin 1 Gene
Also Known as WSS; NFNS; VRNF
Species: Homo sapiens
About NF1
This gene has 39 transcripts (splice variants), 208 orthologues, 10 paralogues and is associated with 219 phenotypes. Ubiquitous expression in thyroid (RPKM 9.3), brain (RPKM 8.2) and 25 other tissues.
Summary
This gene product appears to function as a negative regulator of the Ras signal transduction pathway. Mutations in this gene have been linked to neurofibromatosis type 1, juvenile myelomonocytic leukemia and Watson syndrome. The mRNA for this gene is subject to RNA editing (CGA>UGA->Arg1306Term) resulting in premature translation termination. Alternatively spliced transcript variants encoding different isoforms have also been described for this gene. [provided by RefSeq, Jul 2008]
NF1 Products (3)
| mRNA | Protein | Name |
|---|---|---|
| NM_000267.3 | NP_000258.1 | neurofibromin isoform 2 |
| NM_001042492.3 | NP_001035957.1 | neurofibromin isoform 1 |
| NM_001128147.3 | NP_001121619.1 | neurofibromin isoform 3 |
| Molecular Function GO Annotation | Evidence | Références | Source |
|---|---|---|---|
| enables GTPase activator activity |
IDA
IDA: Inferred from direct assay
|
1568247 | GOA |
| enables phosphatidylcholine binding |
IDA
IDA: Inferred from direct assay
|
17187824 | GOA |
| enables phosphatidylethanolamine binding |
IDA
IDA: Inferred from direct assay
|
17187824 | GOA |
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
11356864 | GOA |
| Cellular Component GO Annotation | Evidence | Références | Source |
|---|---|---|---|
| located in axon |
IDA
IDA: Inferred from direct assay
|
1550670 | GOA |
| located in dendrite |
IDA
IDA: Inferred from direct assay
|
1550670 | GOA |
NF1 Protein Structure
RasGAP: GTPase-activator protein for Ras-like GTPase (1256 - 1430)
CRAL_TRIO_2: Divergent CRAL/TRIO domain (1571 - 1709)
- 0
- 500
- 1000
- 1500
- 2000
- 2500
- 2818 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
neurofibromin |
|
NF1 Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | Références |
|---|---|---|---|---|---|---|---|
|
Intra
|
NF1 | P21359 | SDC2 | Homo sapiens | P34741 | 11356864 | |
|
Intra
|
NF1 | P21359 | SPRED1 | Homo sapiens | Q7Z699 | 26635368 | |
|
Intra
|
NF1 | P21359 | APP | Homo sapiens | P05067 | 16374483 | |
|
Intra
|
NF1 | P21359 | APP | Homo sapiens | P05067 | 16374483 |
NF1 Anticorps
| Cat. No. | Nom du produit | Application | Reactivity |
|---|---|---|---|
| HY-P810903 | NF1 Antibody | WB, IHC-P, ICC/IF | Human, Mouse, Rat |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Neurofibromatosis-Noonan Syndrome |
|
|
| Neurofibromatosis, Type I |
|
|
| Neurofibromatosis, Familial Spinal |
|
|
| Juvenile Myelomonocytic Leukemia |
|
|
| Watson Syndrome |
|
|
| Neurofibromatosis |
|
|
| Neurofibroma |
|
|
| Pilocytic Astrocytoma |
|
|
| Cafe-Au-Lait Spots, Multiple |
|
|
| Optic Nerve Glioma |
|
|
| Lymph Node Disease |
|
|
| Pleomorphic Rhabdomyosarcoma |
|
|
| Rhabdomyosarcoma |
|
|
| Inguinal Hernia |
|
|
| Embryonal Rhabdomyosarcoma |
|
|
| Ewing Sarcoma |
|
|
| Skin Disease |
|
|
| Rhabdomyosarcoma 2 |
|
|
| Specific Learning Disability |
|
|
| Hereditary Paraganglioma-Pheochromocytoma Syndromes |
|
|
| Bap1 Tumor Predisposition Syndrome |
|
|
| Inherited Cancer-Predisposing Syndrome |
|
|
| Malignant Peripheral Nerve Sheath Tumor |
|
|
| Plexiform Neurofibroma |
|
|
| Chromosome 17q11.2 Deletion Syndrome |
|
|
| Neurofibrosarcoma |
|
|
| Ganglioglioma |
|
|
| Chromosome 17q11.2 Duplication Syndrome, 1.4-Mb |
|
|
| Atypical Coarctation Of Aorta |
|
|
| Neurilemmoma |
|
|
| Optic Nerve Neoplasm |
|
|
| Rasopathy |
|
|
| Acoustic Neuroma |
|
|
| Cranial Nerve Malignant Neoplasm |
|
|
| Atypical Neurofibroma |
|
|
| Tuberous Sclerosis |
|
|
| Pulsating Exophthalmos |
|
|
| Paraganglioma |
|
|
| Leukemia |
|
|
| Multiple Endocrine Neoplasia |
|
|
| Childhood Malignant Schwannoma |
|
|
| Pulmonic Stenosis |
|
|
| Serous Cystadenocarcinoma |
|
|
| Adult Malignant Schwannoma |
|
|
| Pheochromocytoma |
|
|
| Cellular Neurofibroma |
|
|
| Autism Spectrum Disorder |
|
|
| Pacinian Tumor |
|
|
| Plasma Cell Neoplasm |
|
|
| Legius Syndrome |
|
|
| Ectropion |
|
|
| Optic Nerve Astrocytoma |
|
|
| Giant Cell Reparative Granuloma |
|
|
| Equatorial Staphyloma |
|
|
| Hereditary Breast Ovarian Cancer Syndrome |
|
|
| Vagus Nerve Neoplasm |
|
|
| Chronic Myelomonocytic Leukemia |
|
|
| Mechanical Ectropion |
|
|
| Myelodysplastic Syndrome |
|
|
| Glossopharyngeal Nerve Neoplasm |
|
|
| Brachial Plexus Neoplasm |
|
|
| Facial Nerve Neoplasm |
|
|
| Nerve Plexus Neoplasm |
|
|
| Multiple Endocrine Neoplasia, Type Iia |
|
|
| Malignant Triton Tumor |
|
|
| Von Hippel-Lindau Syndrome |
|
|
| Orbital Cancer |
|
|
| Duodenal Somatostatinoma |
|
|
| Myeloma, Multiple |
|
|
| Plexiform Schwannoma |
|
|
| Neurilemmomatosis |
|
|
| Epithelioid Neurofibroma |
|
|
| Peripheral Nervous System Benign Neoplasm |
|
|
| Autonomic Nervous System Benign Neoplasm |
|
|
| Meningocele |
|
|
| Noonan Syndrome 1 |
|
|
| Ovarian Serous Cystadenocarcinoma |
|
|
| Fibroma |
|
|
| Glioblastoma |
|
|
| Cowden Syndrome 1 |
|
|
| Juvenile Pilocytic Astrocytoma |
|
|
| Spinal Cancer |
|
|
| Myelodysplastic/Myeloproliferative Neoplasm |
|
|
| Oligodendroglioma |
|
|
| Meningioma, Familial |
|
|
| Cerebellar Astrocytoma |
|
|
| Peripheral Nervous System Neoplasm |
|
|
| Neurofibromatosis, Type Ii |
|
|
| Epithelioid Malignant Peripheral Nerve Sheath Tumor |
|
|
| Central Nervous System Benign Neoplasm |
|
|
| Orbit Embryonal Rhabdomyosarcoma |
|
|
| Pancreatic Somatostatinoma |
|
|
| Persistent Generalized Lymphadenopathy |
|
|
| Malignant Spindle Cell Melanoma |
|
|
| Melanoma |
|
|
| Multiple Endocrine Neoplasia, Type Iib |
|
|
| Malignant Glandular Tumor Of Peripheral Nerve Sheath |
|
|
| Obstructive Hydrocephalus |
|
|
| Childhood Pilocytic Astrocytoma |
|
|
| Small Intestine Leiomyoma |
|
|
| Paraganglioma And Gastric Stromal Sarcoma |
|
|
| Colorectal Cancer |
|
|
| Uterine Corpus Endometrial Carcinoma |
|
|
| Cellular Schwannoma |
|
|
| Fibrillary Astrocytoma |
|
|
| Orbital Disease |
|
|
| Low Grade Glioma |
|
|
| Optic Nerve Sheath Meningioma |
|
|
| Peripheral Nerve Schwannoma |
|
|
| Myeloproliferative Neoplasm |
|
|
| Spinal Cord Disease |
|
|
| Horner'S Syndrome |
|
|
| Cystadenocarcinoma |
|
|
| Orbit Rhabdomyosarcoma |
|
|
| Li-Fraumeni Syndrome |
|
|
| Turner Syndrome |
|
|
| Neurilemmoma Of The Fifth Cranial Nerve |
|
|
| Trigeminal Nerve Neoplasm |
|
|
| Glioma |
|
|
| Pilomyxoid Astrocytoma |
|
|
| Hypomelanosis Of Ito |
|
|
| Liposarcoma |
|
|
| Leiomyosarcoma |
|
|
| Moyamoya Disease 1 |
|
|
| Mucosal Melanoma |
|
|
| Spinal Cord Astrocytoma |
|
|
| Pilocytic Astrocytoma Of Cerebellum |
|
|
| Vulvar Melanoma |
|
|
| Brain Glioma |
|
|
| Neuroendocrine Tumor |
|
|
| Scoliosis |
|
|
| Pleomorphic Xanthoastrocytoma |
|
|
| Malignant Pheochromocytoma |
|
|
| Adrenal Medulla Cancer |
|
|
| Noonan Syndrome With Multiple Lentigines |
|
|
| Schwannoma Of Twelfth Cranial Nerve |
|
|
| Hypoglossal Nerve Disease |
|
|
| Autism |
|
|
| Fragile X Syndrome |
|
|
| Dysembryoplastic Neuroepithelial Tumor |
|
|
| Subependymal Glioma |
|
|
| Cerebellum Cancer |
|
|
| Subungual Glomus Tumor |
|
|
| Perianal Hematoma |
|
|
| Small Intestine Cancer |
|
|
| Cardiofaciocutaneous Syndrome 1 |
|
|
| Multiple Mucosal Neuroma |
|
|
| Amelogenesis Imperfecta |
|
|
| Sturge-Weber Syndrome |
|
|
| Cardiovascular Organ Benign Neoplasm |
|
|
| Proteus Syndrome |
|
|
| Benign Ependymoma |
|
|
| Multiple Endocrine Neoplasia, Type I |
|
|
| Ossifying Fibroma |
|
|
| Bone Structure Disease |
|
|
| Extra-Adrenal Pheochromocytoma |
|
|
| Intermittent Proptosis |
|
|
| Learning Disability |
|
|
| Malignant Conjunctival Melanoma |
|
|
| Non-Langerhans-Cell Histiocytosis |
|
|
| Diffuse Astrocytoma |
|
|
| Skin Benign Neoplasm |
|
|
| Breast Cancer |
|
|
| Somatostatinoma |
|
|
| Costello Syndrome |
|
|
| Epidural Spinal Canal Neoplasm |
|
|
| Idh-Wildtype Glioblastoma |
|
|
| Glomus Tumor |
|
|
| Adrenal Carcinoma |
|
|
| Constipation |
|
|
| Skin Lipoma |
|
|
| Conjunctival Cancer |
|
|
| Exophthalmos |
|
|
| Chondroma |
|
|
| Lipomatosis, Multiple |
|
|
| Conjunctival Nevus |
|
|
| Brain Stem Cancer |
|
|
| Elephantiasis |
|
|
| Rett Syndrome |
|
|
| Spinal Meningioma |
|
|
| Spinal Canal And Spinal Cord Meningioma |
|
|
| Sarcoma, Synovial |
|
|
| Neuroma |
|
|
| Endocrine Organ Benign Neoplasm |
|
|
| Subependymal Giant Cell Astrocytoma |
|
|
| Inflammatory Leiomyosarcoma |
|
|
| Brain Cancer |
|
|
| Familial Retinoblastoma |
|
|
| Nodular Malignant Melanoma |
|
|
| Brachial Plexus Lesion |
|
|
| Skeletal Muscle Cancer |
|
|
| Malignant Skin Fibrous Histiocytoma |
|
|
| Malignant Dermis Tumor |
|
|
| Acral Lentiginous Melanoma |
|
|
| Syringomyelia |
|
|
| Cerebral Arterial Disease |
|
|
| Lumbosacral Plexus Lesion |
|
|
| Muscle Cancer |
|
|
| Choroid Cancer |
|
|
| Chest Wall Lipoma |
|
|
| Enophthalmos |
|
|
| Spinal Cord Glioma |
|
|
| Thyroid Gland Cancer |
|
|
| Basal Cell Nevus Syndrome |
|
|
| Mixed Glioma |
|
|
| Duodenum Cancer |
|
|
| Peripheral Nervous System Disease |
|
|
| Intracranial Meningioma |
|
|
| Arteriovenous Malformation |
|
|
| Connective Tissue Benign Neoplasm |
|
|
| Keratosis Pilaris Atrophicans Faciei |
|
|
| Dicer1 Syndrome |
|
|
| Cowden Syndrome |
|
|
| Mesenchymal Cell Neoplasm |
|
|
| Glaucoma 3, Primary Congenital, A |
|
|
| Gastrointestinal Stromal Tumor |
|
|
| Spindle Cell Sarcoma |
|
|
| Schimmelpenning-Feuerstein-Mims Syndrome |
|
|
| Carney Complex Variant |
|
|
| Diamond-Blackfan Anemia 11 |
|
|
| Endometrial Cancer |
|
|
| Mccune-Albright Syndrome |
|
|
| Klippel-Trenaunay-Weber Syndrome |
|
|
| Myxofibrosarcoma |
|
|
| Medulloblastoma |
|
|
| Nevus, Epidermal |
|
|
| Anaplastic Oligodendroglioma |
|
|
| Cranial Nerve Disease |
|
|
| Neural Tube Defects |
|
|
| Diffuse Midline Glioma, H3 K27m-Mutant |
|
|
| Well-Differentiated Liposarcoma |
|
|
| Multiple Enchondromatosis, Maffucci Type |
|
|
| Dedifferentiated Liposarcoma |
|
|
| Neuroblastoma |
|
|
| Ocular Melanoma |
|
|
| Infratentorial Cancer |
|
|
| Spinal Cord Oligodendroglioma |
|
|
| Gastric Liposarcoma |
|
|
| Anaplastic Astrocytoma |
|
|
| Cell Type Benign Neoplasm |
|
|
| Leukemia, Chronic Myeloid |
|
|
| Giant Cell Glioblastoma |
|
|
| Skin Granular Cell Tumor |
|
|
| Atypical Teratoid Rhabdoid Tumor |
|
|
| Specific Developmental Disorder |
|
|
| Lynch Syndrome |
|
|
| Cerebral Degeneration |
|
|
| Optic Nerve Disease |
|
|
| Gliosarcoma |
|
|
| Melanoma, Cutaneous Malignant 1 |
|
|
| Sotos Syndrome |
|
|
| Polyp Of Corpus Uteri |
|
|
| Rete Ovarii Benign Neoplasm |
|
|
| Rete Ovarii Adenoma |
|
|
| Melanoma, Uveal |
|
|
| Coffin-Siris Syndrome 1 |
|
|
| Attention Deficit-Hyperactivity Disorder |
|
|
| Osteochondrodysplasia |
|
|
| Beckwith-Wiedemann Syndrome |
|
|
| Nervous System Disease |
|
|
| Wilms Tumor 1 |
|
|
| Eye Disease |
|
|
| Connective Tissue Disease |
|
|
| Leukemia, Acute Myeloid |
|
|
| Retinitis Pigmentosa |
|
|
Orthologs Information
| Species | Symbol | Source | ID |
|---|---|---|---|
| Mus musculus | NF1 | MGD | MGI:97306 |
| Rattus norvegicus | NF1 | RGD | RGD:3168 |
| Felis catus | NF1 | VGNC | VGNC:68466 |
| Canis familiaris | NF1 | VGNC | VGNC:43761 |
| Bos taurus | NF1 | VGNC | VGNC:54463 |
| Macaca mulatta | NF1 | VGNC | VGNC:75323 |
| Others | NF1 | NCBI |