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Biological Process
Protein Localization To Nucleus
Diseases Associated With Protein Localization To Nucleus
Disease
Prostatic Neoplasms
Craniofacial Abnormalities
Diabetes Mellitus, Type 2
Breast Carcinoma
Hepatocellular Carcinoma
Leukemia, Promyelocytic, Acute
Cell Transformation, Neoplastic
Muscular Dystrophies, Limb-Girdle
Stomach Neoplasms
Muscular Dystrophy, Emery-Dreifuss
Myocardial Ischemia
Neoplasm Invasiveness
Liver Cirrhosis, Experimental
Left Ventricular Hypertrophy
Precancerous Conditions
Hiv Infections
Colorectal Cancer
Hand Deformities, Congenital
Campomelic Dysplasia
Carcinoma
Basal Cell Carcinoma
Carcinoma, Non-Small-Cell Lung
Renal Cell Carcinoma
Dilated Cardiomyopathy
Charcot-Marie-Tooth Disease, Type 2b1
Cholangitis
Coloboma
Congenital Abnormalities
Corneal Dystrophy, Fleck
Coronary Artery Disease
Deafness, Autosomal Dominant 23
Sudden Cardiac Arrest
Diabetes Mellitus
Diabetes Mellitus, Experimental
Diamond-Blackfan Anemia 7
Disease Progression
Limb Dystonia
Dystonia Musculorum Deformans Type 1
Dystonic Disorders
Ehlers-Danlos Syndrome Type 1
Ehlers-Danlos Syndrome, Type Vii, Autosomal Dominant
Endometriosis
Esophageal Squamous Cell Carcinoma
Eye Abnormalities
Fatty Liver
Femoral Fractures
Fibrosis
Foot Deformities, Congenital
Heart Block
Heart-Hand Syndrome, Slovenian Type
Heart Valve Diseases
Hernia, Diaphragmatic
Hiv-Associated Lipodystrophy Syndrome
Cyclopia
Holoprosencephaly 3
Hyperinsulinism
Hyperlipidemias
Hyperostosis, Cortical, Congenital
Hypertension
Hypertriglyceridemia
Male Infertility
Insulin Resistance
Jaw Abnormalities
Keloid
Limb-Girdle Muscular Dystrophy, Type 1b
Lipodystrophy, Familial Partial
Liver Cirrhosis
Mammary Neoplasms, Animal
Mammary Neoplasms, Experimental
Mandibuloacral Dysplasia With Type A Lipodystrophy
Maxillary Neoplasms
Melanoma
Melanoma, Experimental
Meningioma
Microphthalmia, Isolated, With Coloboma 5
Microphthalmia, Syndromic 6
Muscular Dystrophy, Congenital, Lmna-Related
Nephrogenic Fibrosing Dermopathy
Nephrotic Syndrome
Neuroectodermal Tumors, Primitive
Obesity
Oral Submucous Fibrosis
Orofacial Cleft 11
Orofacial Cleft 5
Osteoarthritis
Osteogenesis Imperfecta
Osteogenesis Imperfecta, Type 2a
Osteogenesis Imperfecta, Type 3
Osteogenesis Imperfecta, Type 4
Osteoporosis
Osteosarcoma
Parkinson Disease, Secondary
Pierre Robin Syndrome
Polycystic Ovary Syndrome
Progeria
Prolactinoma
Pulmonary Fibrosis
Retinitis Pigmentosa 31
Scleroderma, Localized
Single Upper Central Incisor
Sinoatrial Block
Skeletal Defects, Genital Hypoplasia, And Mental Retardation
Skin Neoplasms
Tachycardia, Ventricular
Tight Skin Contracture Syndrome, Lethal
Tooth Abnormalities
Vitamin A Deficiency
Werner Syndrome
Witkop Syndrome
Abortion, Spontaneous
Wittwer Syndrome
Acth-Secreting Pituitary Adenoma
Lung Adenocarcinoma
Alzheimer's Disease
Ameloblastoma
Aneurysm, Dissecting
Anodontia
Anonychia Congenita
Aortic Valve Insufficiency
Psoriatic Arthritis
Rheumatoid Arthritis
Atrial Fibrillation
Autism Spectrum Disorder
Autoimmune Disease
Bone Resorption
Brain Neoplasms
Branchiootic Syndrome 3
Calcinosis
Related Genes
ABCA7
BANP
BMP4
BMP7
CALR
CNEP1R1
COL1A1
DNAJB6
HHEX
LMNA
MDM2
MSX1
PLRG1
SHH
SIX1
SIX4
SMO
SOX9
SYNE2
TOPORS
TOR1A
XPO1
ZBTB16
