INS - insulin Gene
Also Known as IDDM; ILPR; IRDN; IDDM1; IDDM2; PNDM4; MODY10
Species: Homo sapiens
About INS
This gene has 5 transcripts (splice variants), 255 orthologues, 2 paralogues and is associated with 6 phenotypes. Restricted expression toward pancreas (RPKM 671.7).
Summary
This gene encodes Insulin, a peptide hormone that plays a vital role in the regulation of carbohydrate and lipid metabolism. After removal of the precursor signal peptide, proinsulin is post-translationally cleaved into three peptides: the B chain and A chain peptides, which are covalently linked via two disulfide bonds to form Insulin, and C-peptide. Binding of Insulin to the Insulin Receptor (INSR) stimulates glucose uptake. A multitude of mutant alleles with phenotypic effects have been identified, including insulin-dependent diabetes mellitus, permanent neonatal diabetes diabetes mellitus, maturity-onset diabetes of the young type 10 and hyperproinsulinemia. There is a read-through gene, INS-IGF2, which overlaps with this gene at the 5' region and with the IGF2 gene at the 3' region. [provided by RefSeq, May 2020]
INS Products (4)
| mRNA | Protein | Name |
|---|---|---|
| NM_000207.3 | NP_000198.1 | insulin preproprotein |
| NM_001185097.2 | NP_001172026.1 | insulin preproprotein |
| NM_001185098.2 | NP_001172027.1 | insulin preproprotein |
| NM_001291897.2 | NP_001278826.1 | insulin preproprotein |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables hormone activity |
IMP
IMP: Inferred from mutant phenotype
|
381941 | GOA |
| enables identical protein binding |
IPI
IPI: Inferred from physical interaction
|
17472440 | GOA |
| enables insulin receptor binding |
IDA
IDA: Inferred from direct assay
|
7556975 | GOA |
| enables insulin receptor binding |
IPI
IPI: Inferred from physical interaction
|
8452530 | GOA |
| enables insulin-like growth factor receptor binding |
IPI
IPI: Inferred from physical interaction
|
8452530 | GOA |
| enables protease binding |
IPI
IPI: Inferred from physical interaction
|
20082125 | GOA |
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
9388210 | GOA |
| Cellular Component GO Annotation | Evidence | References | Source |
|---|---|---|---|
| located in extracellular space |
IDA
IDA: Inferred from direct assay
|
9667398 | GOA |
INS Protein Structure
Insulin: Insulin/IGF/Relaxin family (28 - 109)
- 0
- 100
- 110 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
insulin |
|
INS Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | References |
|---|---|---|---|---|---|---|---|
|
Intra
|
INS | P01308 | ADAMTSL4 | Homo sapiens | Q6UY14-3 | 32296183 | |
|
Intra
|
INS | P01308 | ADAMTSL4 | Homo sapiens | Q6UY14-3 | 32296183 | |
|
Intra
|
INS | P01308 | ADAMTSL4 | Homo sapiens | Q6UY14-3 | 32296183 | |
|
Intra
|
INS | P01308 | KRTAP1-3 | Homo sapiens | Q8IUG1 | 32296183 | |
|
Intra
|
INS | P01308 | KRTAP1-3 | Homo sapiens | Q8IUG1 | 32296183 | |
|
Intra
|
INS | P01308 | KRTAP1-1 | Homo sapiens | Q07627 | 32296183 | |
|
Intra
|
INS | P01308 | KRTAP1-1 | Homo sapiens | Q07627 | 32296183 | |
|
Intra
|
INS | P01308 | KRTAP1-1 | Homo sapiens | Q07627 | 32296183 | |
|
Intra
|
INS | P01308 | IDE | Homo sapiens | P14735-1 | 17051221 | |
|
Intra
|
INS | P01308 | IDE | Homo sapiens | P14735-1 | 17051221 | |
|
Intra
|
INS | P01308 | IDE | Homo sapiens | P14735-1 | 17051221 | |
|
Intra
|
INS | P01308 | NOTCH2NLC | Homo sapiens | P0DPK4 | 32296183 | |
|
Intra
|
INS | P01308 | NOTCH2NLC | Homo sapiens | P0DPK4 | 32296183 | |
|
Intra
|
INS | P01308 | NOTCH2NLC | Homo sapiens | P0DPK4 | 32296183 | |
|
Intra
|
INS | P01308 | CYSRT1 | Homo sapiens | A8MQ03 | 32296183 | |
|
Intra
|
INS | P01308 | CYSRT1 | Homo sapiens | A8MQ03 | 32296183 | |
|
Intra
|
INS | P01308 | INS | Homo sapiens | P01308 | 20738396 | |
|
Intra
|
INS | P01308 | INS | Homo sapiens | P01308 | 20738396 | |
|
Intra
|
INS | P01308 | INS | Homo sapiens | P01308 | 23106816 | |
|
Intra
|
INS | P01308 | INS | Homo sapiens | P01308 | 20738396 | |
|
Intra
|
INS | P01308 | INS | Homo sapiens | P01308 | 23106816 | |
|
Intra
|
INS | P01308 | INS | Homo sapiens | P01308 | 10508408 | |
|
Intra
|
INS | P01308 | INS | Homo sapiens | P01308 | 23510797 | |
|
Intra
|
INS | P01308 | INS | Homo sapiens | P01308 | 20738396 | |
|
Intra
|
INS | P01308 | INS | Homo sapiens | P01308 | 17472440 | |
|
Intra
|
INS | P01308 | INS | Homo sapiens | P01308 | 23416304 | |
|
Intra
|
INS | P01308 | INS | Homo sapiens | P01308 | 23416304 | |
|
Intra
|
INS | P01308 | INS | Homo sapiens | P01308 | 23106816 | |
|
Intra
|
INS | P01308 | INS | Homo sapiens | P01308 | 22854022 | |
|
Intra
|
INS | P01308 | INS | Homo sapiens | P01308 | 17472440 | |
|
Intra
|
INS | P01308 | INS | Homo sapiens | P01308 | 20738396 | |
|
Intra
|
INS | P01308 | INSR | Homo sapiens | P06213-2 | 23302862 | |
|
Intra
|
INS | P01308 | INSR | Homo sapiens | P06213-2 | 29512653 | |
|
Intra
|
INS | P01308 | INS | Homo sapiens | P01308 | 8844841 |
Recombinant INS Proteins
| Cat. No. | Product Name | Accession | Purity |
|---|---|---|---|
| HY-P73243 | Insulin Protein, Human (P.pastoris) | P01308-1 (F25-K53&G90-N110) | ≥ 95%, as determined by reducing SDS-PAGE. |
INS Antibodies
| Cat. No. | Product Name | Application | Reactivity |
|---|---|---|---|
| HY-P80190 | Insulin Antibody (YA723) | IHC-P, ELISA | Human |
| HY-P86130 | Insulin Antibody (YA5822) | WB, IHC-P, ICC/IF, IP, ELISA | Human, Mouse, Rat |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Maturity-Onset Diabetes Of The Young, Type 10 |
|
|
| Hyperproinsulinemia |
|
|
| Diabetes Mellitus, Permanent Neonatal, 4 |
|
|
| Type 1 Diabetes Mellitus 2 |
|
|
| Permanent Neonatal Diabetes Mellitus |
|
|
| Diabetes Mellitus, Permanent Neonatal, 1 |
|
|
| Isolated Permanent Neonatal Diabetes Mellitus |
|
|
| Maturity-Onset Diabetes Of The Young |
|
|
| Neonatal Diabetes |
|
|
| Type 1 Diabetes Mellitus |
|
|
| Prediabetes Syndrome |
|
|
| Hyperglycemia |
|
|
| Anovulation |
|
|
| Glucose Intolerance |
|
|
| Gestational Diabetes |
|
|
| Diabetes Mellitus |
|
|
| Carbohydrate Metabolic Disorder |
|
|
| Hyperinsulinism |
|
|
| Fetal Macrosomia |
|
|
| Hyperandrogenism |
|
|
| Diabetic Neuropathy |
|
|
| Hypoglycemic Coma |
|
|
| Polycystic Ovary Syndrome |
|
|
| Diabetes Mellitus, Ketosis-Prone |
|
|
| Acanthosis Nigricans |
|
|
| Overnutrition |
|
|
| Hypoglycemia |
|
|
| Donohue Syndrome |
|
|
| Monogenic Diabetes |
|
|
| Fatty Liver Disease |
|
|
| Autonomic Neuropathy |
|
|
| Abdominal Obesity-Metabolic Syndrome 1 |
|
|
| Maturity-Onset Diabetes Of The Young, Type 2 |
|
|
| Ovarian Disease |
|
|
| Leptin Deficiency Or Dysfunction |
|
|
| Insulinoma |
|
|
| Hyperuricemia |
|
|
| Pancreatic Cystadenoma |
|
|
| Microvascular Complications Of Diabetes 5 |
|
|
| Brittle Diabetes |
|
|
| Liver Disease |
|
|
| Stiff-Person Syndrome |
|
|
| Diabetic Angiopathy |
|
|
| Hirata Disease |
|
|
| Type 1 Diabetes Mellitus 5 |
|
|
| Vascular Disease |
|
|
| Lipid Metabolism Disorder |
|
|
| Acromegaly |
|
|
| Type 2 Diabetes Mellitus |
|
|
| Dumping Syndrome |
|
|
| Duodenitis |
|
|
| Monocarboxylate Transporter 1 Deficiency |
|
|
| Autoimmune Polyendocrine Syndrome, Type Ii |
|
|
| Hypopituitarism |
|
|
| Cardiovascular System Disease |
|
|
| Insulin-Like Growth Factor I |
|
|
| Sleep Apnea |
|
|
| Diabetic Encephalopathy |
|
|
| Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, And Somatic Abnormalities |
|
|
| Critical Illness Polyneuropathy |
|
|
| Alcoholic Ketoacidosis |
|
|
| Factitious Disorder |
|
|
| Hyperinsulinemic Hypoglycemia |
|
|
| Inflammatory And Toxic Neuropathy |
|
|
| Autoimmune Disease Of Endocrine System |
|
|
| Pituitary Gland Disease |
|
|
| Pituitary Apoplexy |
|
|
| Non-Alcoholic Fatty Liver Disease |
|
|
| Empty Sella Syndrome |
|
|
| Mandibular Hypoplasia, Deafness, Progeroid Features, And Lipodystrophy Syndrome |
|
|
| Lipodystrophy, Familial Partial, Type 2 |
|
|
| Somatostatinoma |
|
|
| Acquired Metabolic Disease |
|
|
| Atherosclerosis Susceptibility |
|
|
| Nephrosclerosis |
|
|
| Carpal Tunnel Syndrome |
|
|
| Islet Cell Tumor |
|
|
| Congenital Generalized Lipodystrophy |
|
|
| Familial Hyperlipidemia |
|
|
| Severe Nonproliferative Diabetic Retinopathy |
|
|
| Glucose Metabolism Disease |
|
|
| Post-Surgical Hypoinsulinemia |
|
|
| Autoimmune Disease |
|
|
| Scleredema Adultorum |
|
|
| Craniopharyngioma |
|
|
| Gastrinoma |
|
|
| Chronic Fatigue Syndrome |
|
|
| Hypertension, Essential |
|
|
| Hyperprolactinemia |
|
|
| Hyperinsulinemic Hypoglycemia, Familial, 2 |
|
|
| Background Diabetic Retinopathy |
|
|
| Amenorrhea |
|
|
| Inherited Metabolic Disorder |
|
|
| Familial Partial Lipodystrophy |
|
|
| Silent Myocardial Infarction |
|
|
| Hypogonadism |
|
|
| Acne |
|
|
| Kidney Disease |
|
|
| Diabetes Insipidus |
|
|
| Functional Gastric Disease |
|
|
| Hypokalemia |
|
|
| Adult Syndrome |
|
|
| Sebaceous Gland Disease |
|
|
| Duodenal Ulcer |
|
|
| Lipoprotein Quantitative Trait Locus |
|
|
| Arteriosclerosis |
|
|
| Angina Pectoris |
|
|
| Hyperlipidemia, Familial Combined, 3 |
|
|
| Aromatase Deficiency |
|
|
| Pigmentation Disease |
|
|
| Hyperthyroidism |
|
|
| Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 |
|
|
| Ovarian Hyperstimulation Syndrome |
|
|
| Autonomic Nervous System Disease |
|
|
| Uremia |
|
|
| Postgastrectomy Syndrome |
|
|
| Pellagra |
|
|
| Cholelithiasis |
|
|
| Skin Tag |
|
|
| Fanconi-Bickel Syndrome |
|
|
| Bulimia Nervosa |
|
|
| Gastrointestinal System Benign Neoplasm |
|
|
| Turner Syndrome |
|
|
| Alcoholic Liver Cirrhosis |
|
|
| Apnea, Obstructive Sleep |
|
|
| Body Mass Index Quantitative Trait Locus 11 |
|
|
| Thyroiditis |
|
|
| Diabetic Autonomic Neuropathy |
|
|
| Polyneuropathy In Collagen Vascular Disease |
|
|
| Olfactory Nerve Disease |
|
|
| Malignant Otitis Externa |
|
|
| Diabetic Polyneuropathy |
|
|
| Costello Syndrome |
|
|
| Schizoaffective Disorder |
|
|
| Hypertriglyceridemia 1 |
|
|
| Dermatitis, Atopic, 6 |
|
|
| Lipid Storage Disease |
|
|
| Necrobiosis Lipoidica |
|
|
| Congestive Heart Failure |
|
|
| Teratoma |
|
|
| Glycogen Storage Disease |
|
|
| Cholera |
|
|
| Microvascular Complications Of Diabetes 3 |
|
|
| Macular Retinal Edema |
|
|
| Gout |
|
|
| Acute Pancreatitis |
|
|
| Coronary Heart Disease 1 |
|
|
| Cystinosis |
|
|
| Prolactinoma |
|
|
| Generalized Atherosclerosis |
|
|
| Anorexia Nervosa |
|
|
| Goiter |
|
|
| Cavernous Sinus Thrombosis |
|
|
| Sleep Disorder |
|
|
| Hypoparathyroidism |
|
|
| Retinal Microaneurysm |
|
|
| Nephrolithiasis |
|
|
| Pancreatitis |
|
|
| Non-Alcoholic Steatohepatitis |
|
|
| Prader-Willi Syndrome |
|
|
| Marasmus |
|
|
| Hyperpituitarism |
|
|
| Chronic Kidney Disease |
|
|
| Fibromyalgia |
|
|
| Type 1 Diabetes Mellitus 6 |
|
|
| Sheehan Syndrome |
|
|
| Kidney Hypertrophy |
|
|
| Retinal Vascular Disease |
|
|
| Adrenal Gland Disease |
|
|
| Lymphopenia |
|
|
| Alopecia-Intellectual Disability Syndrome 2 |
|
|
| Urinary Tract Infection |
|
|
| Fascioliasis |
|
|
| Retroperitoneal Hemangiopericytoma |
|
|
| Peripheral Artery Disease |
|
|
| Beta-Thalassemia |
|
|
| Lens Disease |
|
|
| Beckwith-Wiedemann Syndrome |
|
|
| Liver Cirrhosis |
|
|
| Tuberous Sclerosis |
|
|
| Acute Orbital Inflammation |
|
|
| Orbital Cellulitis |
|
|
| Wolfram Syndrome 1 |
|
|
| Heart Disease |
|
|
| Thalassemia |
|
|
| Hypothyroidism |
|
|
| Amyloidosis |
|
|
| Mediastinitis |
|
|
| Mucormycosis |
|
|
| Thyroid Gland Disease |
|
|
| Diabetic Cataract |
|
|
| Persistent Fetal Circulation Syndrome |
|
|
| Renal Glucosuria |
|
|
| Maturity-Onset Diabetes Of The Young, Type 3 |
|
|
| Familial Hypercholesterolemia |
|
|
| Transient Neonatal Diabetes Mellitus |
|
|
| Graves Disease 1 |
|
|
| Motor Neuron Disease |
|
|
| Acute Myocardial Infarction |
|
|
| Ovarian Stromal Hyperthecosis |
|
|
| Type 1 Diabetes Mellitus 4 |
|
|
| Amyloid Tumor |
|
|
| Hypothalamic Disease |
|
|
| Maturity-Onset Diabetes Of The Young, Type 1 |
|
|
| Diabetic Macular Edema |
|
|
| Type 1 Diabetes Mellitus 3 |
|
|
| Conn'S Syndrome |
|
|
| Hypogonadotropic Hypogonadism 24 With Or Without Anosmia |
|
|
| Mineral Metabolism Disease |
|
|
| Androgenic Alopecia |
|
|
| Complete Generalized Lipodystrophy |
|
|
| Balanitis |
|
|
| Anxiety |
|
|
| Arteries, Anomalies Of |
|
|
| Speech And Communication Disorders |
|
|
| Intermediate Coronary Syndrome |
|
|
| Lactose Intolerance |
|
|
| Breast Cancer |
|
|
| Myocardial Infarction |
|
|
| Protein-Deficiency Anemia |
|
|
| Hypogonadotropic Hypogonadism |
|
|
| Adermatoglyphia |
|
|
| Short Syndrome |
|
|
| Neurotic Disorder |
|
|
| Peptic Ulcer Disease |
|
|
| Acquired Generalized Lipodystrophy |
|
|
| Intracranial Sinus Thrombosis |
|
|
| Kwashiorkor |
|
|
| Potter'S Syndrome |
|
|
| Familial Periodic Paralysis |
|
|
| Decubitus Ulcer |
|
|
| Pre-Eclampsia |
|
|
| Peripheral Vascular Disease |
|
|
| Maturity-Onset Diabetes Of The Young, Type 4 |
|
|
| Hypercholesterolemia, Familial, 1 |
|
|
| Rubeosis Iridis |
|
|
| Adrenal Cortical Hypofunction |
|
|
| Asphyxia Neonatorum |
|
|
| Central Pontine Myelinolysis |
|
|
| Vein Disease |
|
|
| Malaria |
|
|
| Neurogenic Arthropathy |
|
|
| Transient Cerebral Ischemia |
|
|
| Pituitary Infarct |
|
|
| Pancreatic Endocrine Carcinoma |
|
|
| Epiphyseal Dysplasia, Multiple, With Early-Onset Diabetes Mellitus |
|
|
| Myxedema |
|
|
| Disorder Of Sexual Development |
|
|
| Acidophil Adenoma |
|
|
| Aspiration Pneumonia |
|
|
| Adrenal Carcinoma |
|
|
| Nasopharyngitis |
|
|
| Deficiency Anemia |
|
|
| Specific Developmental Disorder |
|
|
| Dysthymic Disorder |
|
|
| Substance Abuse |
|
|
| Steroid Inherited Metabolic Disorder |
|
|
| Pancreatic Agenesis |
|
|
| Eating Disorder |
|
|
| Lipodystrophy, Congenital Generalized, Type 2 |
|
|
| Alcohol Use Disorder |
|
|
| Type 1 Diabetes Mellitus 12 |
|
|
| Vulvovaginitis |
|
|
| Osteoporosis |
|
|
| Wolfram Syndrome |
|
|
| Angelman Syndrome |
|
|
| Cataract |
|
|
| Hemorrhoid |
|
|
| Endogenous Depression |
|
|
| Nonobstructive Coronary Artery Disease |
|
|
| Colon Adenocarcinoma |
|
|
| Esophageal Varix |
|
|
| Pernicious Anemia |
|
|
| Parathyroid Gland Disease |
|
|
| Endometrial Cancer |
|
|
| Osteogenesis Imperfecta, Type Xviii |
|
|
| Carotid Artery Disease |
|
|
| Aortic Atherosclerosis |
|
|
| Renal Artery Disease |
|
|
| Disease Of Mental Health |
|
|
| Hernia, Hiatus |
|
|
| Transient Refractive Change |
|
|
| Chronic Ulcer Of Skin |
|
|
| Lysosomal Storage Disease |
|
|
| Cellulitis |
|
|
| Pancreas Disease |
|
|
| Diastolic Heart Failure |
|
|
| Hair Disease |
|
|
| Proteasome-Associated Autoinflammatory Syndrome 1 |
|
|
| Prostatic Hypertrophy |
|
|
| Vitamin B12 Deficiency |
|
|
| Compartment Syndrome |
|
|
| Hypokalemic Periodic Paralysis, Type 1 |
|
|
| Colorectal Cancer |
|
|
| Microvascular Complications Of Diabetes 1 |
|
|
| Nerve Compression Syndrome |
|
|
| Platelet Glycoprotein Iv Deficiency |
|
|
| Metal Metabolism Disorder |
|
|
| Diffuse Idiopathic Skeletal Hyperostosis |
|
|
| Paralytic Ileus |
|
|
| Pyelitis |
|
|
| Lipomatosis |
|
|
| Cystic Fibrosis |
|
|
| Necrotizing Fasciitis |
|
|
| Choline Deficiency Disease |
|
|
| Heart Conduction Disease |
|
|
| Vitamin Metabolic Disorder |
|
|
| Endocrine System Disease |
|
|
| Neovascular Glaucoma |
|
|
| Sensory System Disease |
|
|
| Premature Menopause |
|
|
| Peripheral Nervous System Disease |
|
|
| Systolic Heart Failure |
|
|
| Newborn Respiratory Distress Syndrome |
|
|
| Adrenal Cortex Disease |
|
|
| Premature Ovarian Failure 19 |
|
|
| Fetal Erythroblastosis |
|
|
| Mild Cognitive Impairment |
|
|
| Glycogen Storage Disease Ia |
|
|
| Lipodystrophy, Familial Partial, Type 3 |
|
|
| Nephrotic Syndrome |
|
|
| Bone Resorption Disease |
|
|
| Hypertensive Heart Disease |
|
|
| Lipoid Congenital Adrenal Hyperplasia |
|
|
| Hepatic Vascular Disease |
|
|
| Epilepsy, Idiopathic Generalized 4 |
|
|
| Bone Remodeling Disease |
|
|
| Beriberi |
|
|
| Type 1 Diabetes Mellitus 23 |
|
|
| Type 1 Diabetes Mellitus 8 |
|
|
| Cerebrovascular Disease |
|
|
| Muscular Dystrophy |
|
|
| Cell Type Benign Neoplasm |
|
|
| Major Depressive Disorder |
|
|
| Aromatase Excess Syndrome |
|
|
| Common Variable Immunodeficiency |
|
|
| Pancreatic Cancer |
|
|
| Integumentary System Disease |
|
|
| Vascular Dementia |
|
|
| Renal Hypertension |
|
|
| Type 1 Diabetes Mellitus 15 |
|
|
| Macular Degeneration, Age-Related, 1 |
|
|
| Liver Lipoma |
|
|
| Uterine Benign Neoplasm |
|
|
| Pain Agnosia |
|
|
| Autoimmune Disease Of Gastrointestinal Tract |
|
|
| Substance Dependence |
|
|
| Heart Valve Disease |
|
|
| Systemic Lupus Erythematosus |
|
|
| Agnosia |
|
|
| Mental Depression |
|
|
| Celiac Disease 1 |
|
|
| Placenta Disease |
|
|
| Myopathy |
|
|
| Bilirubin Metabolic Disorder |
|
|
| Retinal Disease |
|
|
| Reproductive Organ Benign Neoplasm |
|
|
| Exudative Vitreoretinopathy 1 |
|
|
| Uvulitis |
|
|
| Neurogenic Bladder |
|
|
| Hemoglobinopathy |
|
|
| Polyhydramnios |
|
|
| Teeth Hard Tissue Disease |
|
|
| Amelogenesis Imperfecta, Type Ig |
|
|
| Bronchial Disease |
|
|
| Alzheimer Disease 9 |
|
|
| Bone Inflammation Disease |
|
|
| Multiple Endocrine Neoplasia, Type I |
|
|
| Hyperlipoproteinemia, Type V |
|
|
| Supine Hypotensive Syndrome |
|
|
| Primary Bacterial Infectious Disease |
|
|
| Schizophrenia |
|
|
| Rhabdomyosarcoma |
|
|
| Beta-Thalassemia Major |
|
|
| Physical Disorder |
|
|
| Gallbladder Disease |
|
|
| Muscular Disease |
|
|
| Ureteric Orifice Cancer |
|
|
| Muscle Tissue Disease |
|
|
| Prostate Cancer |
|
|
| Breast Adenocarcinoma |
|
|
| Hepatocellular Carcinoma |
|
|
| Lactic Acidosis |
|
|
| Ovarian Cancer |
|
|
| Diencephalic Astrocytoma |
|
|
| Neuroblastoma |
|
|
| Ulcer Of Lower Limbs |
|
|
| Glucosephosphate Dehydrogenase Deficiency |
|
|
| Eye Disease |
|
|
| Cryptorchidism, Unilateral Or Bilateral |
|
|
| Constipation |
|
|
| Inguinal Hernia |
|
|
| Patent Ductus Arteriosus 1 |
|
|
| Arthrogryposis, Distal, Type 1c |
|
|
| Chromosomal Duplication Syndrome |
|
|
| Parkinson Disease, Late-Onset |
|
|
| Hypertrichosis |
|
|
| Psychotic Disorder |
|
|
| Hemochromatosis, Type 1 |
|
|
| Migraine With Or Without Aura 1 |
|
|
| Respiratory Failure |
|
|
| Alcohol Dependence |
|
|
| Amelogenesis Imperfecta |
|
|
| Nervous System Disease |
|
|
| Skin Disease |
|
|
| Optic Nerve Disease |
|
|
| Immune Deficiency Disease |
|
|
| Stroke, Ischemic |
|
|
| Atrial Heart Septal Defect |
|
|
| Colonic Benign Neoplasm |
|
|
| Connective Tissue Disease |
|
|
| Patent Foramen Ovale |
|
|
| Attention Deficit-Hyperactivity Disorder |
|
|
| Primary Biliary Cholangitis |
|
|
| Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes |
|
|
| Polycystic Kidney Disease |
|
|
| Alzheimer Disease, Familial, 1 |
|
|
| Osteochondrodysplasia |
|
|
| Hypertrophic Cardiomyopathy |
|
|
| Dilated Cardiomyopathy |
|
|
| Rasopathy |
|
|
| Amyotrophic Lateral Sclerosis 1 |
|
|
| Congenital Nervous System Abnormality |
|
|
| Retinitis Pigmentosa |
|
|
| Fundus Dystrophy |
|
|
Orthologs Information
| Species | Symbol | Source | ID |
|---|---|---|---|
| Felis catus | INS | VGNC | VGNC:82037 |
| Bos taurus | INS | VGNC | VGNC:56268 |
| Canis familiaris | INS | VGNC | VGNC:97204 |
| Macaca mulatta | INS | VGNC | VGNC:101288 |
| Rattus norvegicus | INS | RGD | RGD:2916 |
| Mus musculus | INS | MGD | MGI:96573 |
| Others | INS | NCBI |