Showing entry for SUN domain-containing protein 1



                       
General Target Information
BXGT IdBXGT025393
Protein NameSUN domain-containing protein 1
Uniport IdO94901
GeneSUN1
Gene Id23353
DomainMRP; Sad1_UNC; Sun2_CC2
Pfam PF09387   PF07738   PF18580  
OrganismHomo sapiens (Human)
Target protein  affiliated  biological  pathways
KEGG
Class Subclass KEGG Id Pathway Name
Gene Ontology
GO Type GO Id Gene Ontology
Biological Process GO:0051642 centrosome localization
Biological Process GO:0070197 meiotic attachment of telomere to nuclear envelope
Biological Process GO:0006998 nuclear envelope organization
Biological Process GO:0090292 nuclear matrix anchoring at nuclear membrane
Biological Process GO:0021817 nucleokinesis involved in cell motility in cerebral cortex radial glia guided migration
Biological Process GO:0001503 ossification
Biological Process GO:0009612 response to mechanical stimulus
Biological Process GO:0007283 spermatogenesis
Biological Process GO:0007129 synapsis
molecular function GO:0140444 cytoskeleton-nuclear membrane anchor activity
molecular function GO:0005521 lamin binding
molecular function GO:0043495 protein-membrane adaptor activity
cellular component GO:0005737 cytoplasm
cellular component GO:0005639 integral component of nuclear inner membrane
cellular component GO:0043231 intracellular membrane-bounded organelle
cellular component GO:0034993 meiotic nuclear membrane microtubule tethering complex
cellular component GO:0005635 nuclear envelope
cellular component GO:0031965 nuclear membrane
Reactome
Pathway Id Pathway Name
R-HSA-1221632 Meiotic synapsis
R-HSA-1474165 Reproduction
R-HSA-1500620 Meiosis
R-HSA-1640170 Cell Cycle
Target protein-related  diseases
Disease
CUI Id BXGD Id Disease Name Disease Class
C0004238 BXGD000262 Atrial Fibrillation Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0006142 BXGD000374 Malignant neoplasm of breast Neoplasms; Skin and Connective Tissue Diseases
C0006826 BXGD000408 Malignant Neoplasms Neoplasms
C0013264 BXGD000808 Muscular Dystrophy, Duchenne Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C0019372 BXGD001329 Herpesviridae Infections Infections
C0026848 BXGD001941 Myopathy Musculoskeletal Diseases; Nervous System Diseases
C0026850 BXGD001942 Muscular Dystrophy Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C0033300 BXGD002403 Progeria Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
C0079680 BXGD003085 Lentivirus Infections Infections
C0152013 BXGD003516 Adenocarcinoma of lung (disorder) Neoplasms
C0153392 BXGD003630 Malignant neoplasm of nasopharynx Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases
C0235480 BXGD004751 Paroxysmal atrial fibrillation Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0238301 BXGD004909 Cancer of Nasopharynx Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases
C0410189 BXGD008413 Muscular Dystrophy, Emery-Dreifuss Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C0427460 BXGD008616 Red cell distribution width determination
C0520680 BXGD009102 Sleep Apnea, Central Respiratory Tract Diseases; Nervous System Diseases
C0678222 BXGD009749 Breast Carcinoma Neoplasms; Skin and Connective Tissue Diseases
C0751039 BXGD010302 Cockayne Syndrome, Type I Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases
C1269955 BXGD012005 Tumor Cell Invasion
C1304746 BXGD012343 RDW - Red blood cell distribution width result
C1305855 BXGD012348 Body mass index
C1306459 BXGD012361 Primary malignant neoplasm Neoplasms
C2363741 BXGD017100 HIV-1 infection
C2585653 BXGD017139 Persistent atrial fibrillation Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C2931822 BXGD018068 Nasopharyngeal carcinoma Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases
C3468561 BXGD018908 familial atrial fibrillation Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
Target protein-related  compounds
Compounds
BXGC Id Compound Name Strcuture Molecular Weight
BXGC0002591 Potassium 39.1
The  target protein-related  foods
Foods
BXGF Id Food Name Scientific Name Food Group Number of compound? Number of compound in food, higher numbers indicate the food are more associated with the protein