







Yeast Systematic Name | Yeast Symbol | SGDID | Analog Name | Analog Description | EC | Organism | Disease | Structure | Uniprot | Human ID | Human Symbol | HHsearch Probability | HHsearch E_value | HHsearch P_value | HHsearch Score | Flag Disease related | Flag Homo sapiens | Flag Mus musculus | Flag Danio rerio | Flag Drosophila melanogaster | Flag Caenorhabditis elegans | Flag Arabidopsis thaliana | Flag Escherichia coli |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YBR140C | IRA1 | SGDID:S000000344 | Syngap1 |
Ras/Rap GTPase-activating protein SynGAP (Neuronal RasGAP) (Synaptic Ras GTPase-activating protein 1) (Synaptic Ras-GAP 1) (p135 SynGAP) |
Rattus norvegicus | 3bxj_a | Q9QUH6 | 100.00 | 4.50E-37 | 5.50E-41 | 356.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR140C | IRA1 | SGDID:S000000344 | NF1 |
Neurofibromin (Neurofibromatosis-related protein NF-1) [Cleaved into: Neurofibromin truncated] |
Homo sapiens | Spinal Meningioma,Skin Melanoma,Bone Structure Disease,Learning Disability,Neurofibromatosis, Type Ii,Orbital Cancer,Spinal Canal And Spinal Cord Meningioma,Small Intestine Leiomyoma,Horner'S Syndrome,Polyp Of Corpus Uteri,Facial Nerve Neoplasm,Retinitis Pigmentosa,Brain Stem Cancer,Cerebellum Cancer,Cerebral Hemisphere Lipoma,Corpus Callosum Lipoma,Ossifying Fibroma,Chronic Myelomonocytic Leukemia,Cowden Syndrome,Giant Cell Reparative Granuloma,Peripheral Nervous System Benign Neoplasm,Autonomic Nervous System Benign Neoplasm,Optic Nerve Disease,Acantholytic Acanthoma,Leukemia, Chronic Myeloid,Orbital Disease,Plasma Cell Neoplasm,Dedifferentiated Liposarcoma,Cowden Syndrome 1,Exophthalmos,Breast Juvenile Papillomatosis,Mosaic Trisomy 8,Leiomyosarcoma,Malignant Triton Tumor,Neurofibromatosis-Noonan Syndrome,Peripheral Nervous System Neoplasm,Neuroma,Somatostatinoma,Pancreatic Somatostatinoma,Trigeminal Nerve Neoplasm,Juvenile Pilocytic Astrocytoma,Childhood Pilocytic Astrocytoma,Rete Ovarii Adenoma,Rasopathy,Peripheral Nerve Schwannoma,Vulvar Melanoma,Esophagus Leiomyoma,Keratosis Pilaris Atrophicans Faciei,Neurofibroma,Optic Pathway Glioma,Specific Learning Disability,Costello Syndrome,Amelogenesis Imperfecta,Familial Retinoblastoma,Perianal Hematoma,Myeloproliferative Neoplasm,Nerve Plexus Neoplasm,Perineurioma,Atypical Coarctation Of Aorta,Infratentorial Cancer,Duodenal Somatostatinoma,Pulsating Exophthalmos,Neurofibromatosis, Type I,Leukemia,Chronic Inflammation Of Lacrimal Passage,Neurofibromatosis, Familial Spinal,Dacryocystocele,Lymph Node Disease,Neuroblastoma,Multiple Endocrine Neoplasia, Type Iib,Subependymal Glioma,Benign Ependymoma,Pilomyxoid Astrocytoma,Cerebellar Astrocytoma,Pilocytic Astrocytoma,Pilocytic Astrocytoma Of Cerebellum,Gliofibroma,Diffuse Astrocytoma,Childhood Malignant Schwannoma,Skin Granular Cell Tumor,Rete Ovarii Benign Neoplasm,Nevus, Epidermal,Inherited Cancer-Predisposing Syndrome,Adult Xanthogranuloma,Acoustic Neuroma,Cerebral Falx Meningioma,Glioma,Leukemia, Acute Myeloid,Noonan Syndrome 1,Myelodysplastic/Myeloproliferative Neoplasm,Elephantiasis,Optic Nerve Astrocytoma,Optic Nerve Glioma,Mixed Glioma,Epithelioid Malignant Peripheral Nerve Sheath Tumor,Ganglioglioma,Adult Malignant Schwannoma,Chondroma,Epididymal Neoplasm,Carney Complex Variant,Epithelioid Neurofibroma,Plexiform Neurofibroma,Cellular Neurofibroma,Atypical Neurofibroma,Brachial Plexus Lesion,Basal Cell Nevus Syndrome,Pacinian Tumor,Vagus Nerve Neoplasm,Duodenum Cancer,Hereditary Paraganglioma-Pheochromocytoma Syndromes,Subungual Glomus Tumor,Subglottis Benign Neoplasm,Brain Cancer,Skin Lipoma,Wilms Tumor Predisposition,Ovarian Cancer,Neurofibromatosis,Tuberous Sclerosis,Cafe-Au-Lait Spots, Multiple,Spinal Cancer,Optic Nerve Sheath Meningioma,Urachal Adenocarcinoma,Cranial Nerve Disease,Breast Cancer,Glioblastoma,Hereditary Breast Ovarian Cancer Syndrome,Malignant Astrocytoma,High Grade Glioma,Acute Monoblastic Leukemia,Gliosarcoma,Adrenal Medulla Cancer,Colorectal Cancer,Peripheral Nervous System Disease,Equatorial Staphyloma,Nervous System Cancer,Hypoglossal Nerve Disease,Multiple Endocrine Neoplasia,Lumbosacral Plexus Lesion,Malignant Spindle Cell Melanoma,Skin Benign Neoplasm,Oligodendroglioma,Brachial Plexus Neoplasm,Cardiofaciocutaneous Syndrome 1,Spinal Cord Oligodendroglioma,Meningocele,Spinal Cord Disease,Malignant Peripheral Nerve Sheath Tumor,Neurilemmoma,Microcephaly,Cellular Schwannoma,Schwannoma Of Twelfth Cranial Nerve,Neurilemmoma Of The Fifth Cranial Nerve,Neurilemmomatosis,Pheochromocytoma,Plexiform Schwannoma,Aneurysm,Obstructive Hydrocephalus,Multiple Endocrine Neoplasia, Type Iia,Rhabdomyosarcoma,Orbit Embryonal Rhabdomyosarcoma,Orbit Rhabdomyosarcoma,Syringomyelia,Noonan Syndrome With Multiple Lentigines,Alacrima, Achalasia, And Mental Retardation Syndrome,Enophthalmos,Cranial Nerve Neoplasm,Liposarcoma,Optic Nerve Neoplasm,Subclavian Artery Aneurysm,Skin Carcinoma,Turner Syndrome,Disease Of Mental Health,Chromosome 17q11.2 Deletion Syndrome, 1.4-Mb,Neurofibrosarcoma,Cerebral Arterial Disease,Proteus Syndrome,Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a,Glaucoma 3, Primary Congenital, A,Central Nervous System Cancer,Mechanical Ectropion,Ectropion,Renovascular Hypertension,Craniopharyngioma,Aland Island Eye Disease,Myopathy, Centronuclear, 5,Skeletal Muscle Cancer,Muscle Cancer,Multiple Endocrine Neoplasia, Type I,Sarcoma, Synovial,Neural Tube Defects,Legius Syndrome,Odontochondrodysplasia,Strabismus,Sturge-Weber Syndrome,Myelodysplastic Syndrome,Tumor Predisposition Syndrome,Autosomal Genetic Disease,Ewing Sarcoma,Paraganglioma,Gastrointestinal Stromal Tumor,Paraganglioma And Gastric Stromal Sarcoma,Fibroma,Von Hippel-Lindau Syndrome,Watson Syndrome,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Mucosal Melanoma,Extra-Adrenal Pheochromocytoma,Specific Developmental Disorder,Meningioma, Familial,Autism Spectrum Disorder,Osteofibrous Dysplasia,Endocrine Organ Benign Neoplasm,Central Nervous System Benign Neoplasm,Cardiovascular Organ Benign Neoplasm,Brain Glioma,Chromosome 17q11.2 Duplication Syndrome, 1.4-Mb,Scoliosis,Moyamoya Disease 1,Juvenile Myelomonocytic Leukemia,Li-Fraumeni Syndrome,Lipomatosis, Multiple,Persistent Generalized Lymphadenopathy,Inguinal Hernia,Chromosome 17q11.2 Deletion Syndrome,Rett Syndrome,Myeloma, Multiple,Medulloblastoma,Spinal Disease,Autism,Melanoma, Cutaneous Malignant 1,Melanoma, Uveal,Pulmonic Stenosis |
3pg7_b | P21359 | ENSG00000196712 | NF1 | 100.00 | 2.20E-37 | 2.80E-41 | 329.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR140C | IRA1 | SGDID:S000000344 | IQGAP1 KIAA0051 |
Ras GTPase-activating-like protein IQGAP1 (p195) |
Homo sapiens | Bullous Skin Disease,Colorectal Cancer,Gastric Cancer,Skin Disease,Nephrotic Syndrome, Type 3,Lissencephaly,Wolf-Hirschhorn Syndrome,Leigh Syndrome |
3fay_a | P46940 | ENSG00000140575 | IQGAP1 | 100.00 | 2.60E-37 | 3.10E-41 | 349.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR140C | IRA1 | SGDID:S000000344 | RasGAP |
GTPase-activator protein for Ras-like GTPase |
pfam Family | PF00616 | 99.80 | 1.90E-24 | 2.40E-28 | 222.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |