Not currently registered for phenotyping at IMPC
Phenotyping is currently not planned for a knockout strain of this gene.
Gene Summary
IMPC Data Collections
- No Body Weight Data
- No Embryo Imaging Data
- No Viability Data
Phenotyping is currently not planned for a knockout strain of this gene.
The analysis uses data from IMPC, along with published data on other mouse mutants, in comparison to human disease reports in OMIM, Orphanet, and DECIPHER.
Phenotype comparisons summarize the similarity of mouse phenotypes with human disease phenotypes.
The table below shows human diseases predicted to be associated to Gga2 by phenotypic similarity.
Disease | Similarity of phenotypes |
Matching phenotypes | Source |
---|---|---|---|
Granulomas, Congenital Cerebral | Neonatal death | OMIM:306300 | |
Genitourinary Tract Anomalies | Neonatal death | OMIM:305690 | |
3-Hydroxy-3-Methylglutaryl-Coa Synthase Deficiency | Hypoglycemia | ORPHA:35701 | |
Hyperinsulinemic Hypoglycemia, Familial, 7 | Hypoglycemic seizures, Hyperinsulinemia, Hyperinsulinemic hypoglycemia, Hypoglycemia | OMIM:610021 | |
Hypoinsulinemic Hypoglycemia And Body Hemihypertrophy | Hypoglycemic seizures, Hypoketotic hypoglycemia, Neonatal hypoglycemia, Nonketotic hypoglycemia | ORPHA:293964 | |
Glycogen Storage Disease 0, Liver | Postprandial hyperglycemia, Neonatal hypoglycemia, Fasting hypoglycemia | OMIM:240600 | |
Hyperinsulinism Due To Insr Deficiency | Insulin resistance, Hypoglycemia, Fasting hyperinsulinemia, Recurrent hypoglycemia, Hyperinsuline... | ORPHA:263458 | |
Dwarfism, Low-Birth-Weight Type, With Unresponsiveness To Growth Hormone | Hypoglycemia | OMIM:223500 | |
Fructose And Galactose Intolerance | Hypoglycemia | OMIM:229500 | |
Short Stature Due To Partial Ghr Deficiency | Hypoglycemia | ORPHA:314802 | |
Congenital Glucokinase-Related Hyperinsulinism | Fasting hyperinsulinemia, Recurrent hypoglycemia, Hypoketotic hypoglycemia, Type II diabetes mell... | ORPHA:79299 | |
Hyperinsulinemic Hypoglycemia, Familial, 2 | Hyperinsulinemic hypoglycemia, Hypoglycemia | OMIM:601820 | |
Insulin Autoimmune Syndrome | Insulin resistance, Insulin-resistant diabetes mellitus, Reactive hypoglycemia, Nonketotic hypogl... | ORPHA:411593 | |
Hypoinsulinemic Hypoglycemia With Hemihypertrophy | Fasting hypoglycemia, Hypoinsulinemia, Neonatal hypoglycemia, Hypoglycemia | OMIM:240900 | |
Phosphoenolpyruvate Carboxykinase Deficiency, Mitochondrial | Impaired gluconeogenesis, Hypoglycemia | OMIM:261650 | |
Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency | Hypoglycemia | OMIM:609016 | |
Glycogen Storage Disease Due To Glycogen Debranching Enzyme Deficiency | Hypoglycemia | ORPHA:366 | |
Hypoglycemia, Leucine-Induced | Hyperinsulinemic hypoglycemia, Hypoglycemia | OMIM:240800 | |
Short Stature Due To Ghsr Deficiency | Hypoglycemia | ORPHA:314811 | |
Pulmonary Hypoplasia, Primary | Neonatal death | OMIM:265430 | |
Pituitary Hormone Deficiency, Combined, 4 | Hypoglycemia | OMIM:262700 | |
Isolated Growth Hormone Deficiency, Type Ia | Hypoglycemia | OMIM:262400 | |
Epidermolysis Bullosa With Diaphragmatic Hernia | Neonatal death | OMIM:226735 | |
Maturity-Onset Diabetes Of The Young, Type 3 | Hyperglycemia, Type II diabetes mellitus, Maturity-onset diabetes of the young | OMIM:600496 | |
Hyperinsulinism Due To Hnf1A Deficiency | Maturity-onset diabetes of the young, Hyperinsulinemia, Hypoketotic hypoglycemia, Reactive hypogl... | ORPHA:324575 | |
Diaphragmatic Hernia 5, X-Linked | Neonatal death | OMIM:306950 | |
3-Methylglutaconic Aciduria Type 1 | Hypoglycemia | ORPHA:67046 | |
Mitochondrial Complex Iii Deficiency, Nuclear Type 3 | Hypoglycemia | OMIM:615158 | |
Homozygous 11P15-P14 Deletion Syndrome | Hyperinsulinemia, Hypoglycemia | OMIM:606528 | |
Glycogen Storage Disease Vi | Hypoglycemia | OMIM:232700 | |
Hyperinsulinism-Hyperammonemia Syndrome | Hyperinsulinemic hypoglycemia, Reactive hypoglycemia, Fasting hyperinsulinemia | ORPHA:35878 | |
Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, And Somatic Abnormalities | Postprandial hyperglycemia, Insulin-resistant diabetes mellitus, Hypoglycemia, Hyperglycemia, Hyp... | OMIM:262190 | |
Non-Insulinoma Pancreatogenous Hypoglycemia Syndrome | Hyperinsulinemia, Hypoketotic hypoglycemia, Reactive hypoglycemia, Hyperinsulinemic hypoglycemia,... | ORPHA:276608 | |
Neonatal Hemochromatosis | Hypoglycemia | ORPHA:446 | |
Short Stature-Delayed Bone Age Due To Thyroid Hormone Metabolism Deficiency | Fasting hypoglycemia | ORPHA:171706 | |
Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency | Hypoglycemia | OMIM:610090 | |
Neutropenia, Lethal Congenital, With Eosinophilia | Neonatal death | OMIM:257100 | |
Autosomal Dominant Hyperinsulinism Due To Kir6.2 Deficiency | Type I diabetes mellitus, Hyperinsulinemia, Hypoketotic hypoglycemia, Maternal diabetes, Fasting ... | ORPHA:276580 | |
Hyperinsulinemic Hypoglycemia, Familial, 8 | Hypoglycemic seizures, Hyperinsulinemia, Hypoglycemia | OMIM:620211 | |
Dicarboxylic Aminoaciduria | Fasting hypoglycemia | OMIM:222730 | |
Endocardial Fibroelastosis | Hypoglycemia | ORPHA:2022 | |
Dihydrolipoamide Dehydrogenase Deficiency | Death in childhood, Hypoglycemia | OMIM:246900 | |
Hyperinsulinism Due To Ucp2 Deficiency | Recurrent hypoglycemia, Hypoketotic hypoglycemia, Reactive hypoglycemia, Hyperinsulinemic hypogly... | ORPHA:276556 | |
Combined Oxidative Phosphorylation Deficiency 40 | Hypoglycemia, Death in infancy, Neonatal death | OMIM:618835 | |
Combined Oxidative Phosphorylation Deficiency 42 | Hypoglycemia, Death in infancy, Neonatal death | OMIM:618839 | |
Mitochondrial Complex Iii Deficiency, Nuclear Type 9 | Hypoglycemia | OMIM:616111 | |
Orthostatic Hypotension 2 | Hypoglycemia | OMIM:618182 | |
Diarrhea 13 | Recurrent hypoglycemia | OMIM:620357 | |
Autosomal Dominant Hyperinsulinism Due To Sur1 Deficiency | Type I diabetes mellitus, Hyperinsulinemia, Hypoketotic hypoglycemia, Hyperinsulinemic hypoglycem... | ORPHA:276575 | |
Mitochondrial Dna Depletion Syndrome 9 (Encephalomyopathic Type With Methylmalonic Aciduria) | Hypoglycemia, Death in childhood, Death in infancy, Neonatal death | OMIM:245400 | |
3-Methylcrotonyl-Coa Carboxylase Deficiency | Hypoglycemia | ORPHA:6 | |
Propionic Acidemia | Hypoglycemia | ORPHA:35 | |
Silver-Russell Syndrome Due To An Imprinting Defect Of 11P15 | Neonatal hypoglycemia, Hypoglycemia | ORPHA:231140 | |
Intellectual Developmental Disorder With Macrocephaly, Seizures, And Speech Delay | Recurrent hypoglycemia | OMIM:618158 | |
Silver-Russell Syndrome Due To Maternal Uniparental Disomy Of Chromosome 11 | Hypoglycemia | ORPHA:231147 | |
Isobutyryl-Coa Dehydrogenase Deficiency | Ketotic hypoglycemia | ORPHA:79159 | |
Mehmo Syndrome | Hypoglycemia | OMIM:300148 | |
Mitochondrial Pyruvate Carrier Deficiency | Hypoglycemia | OMIM:614741 | |
3-Methylglutaconic Aciduria Type 4 | Hypoglycemia | ORPHA:67048 | |
Riboflavin Deficiency | Hypoglycemia | OMIM:615026 | |
Monocarboxylate Transporter 1 Deficiency | Ketotic hypoglycemia | OMIM:616095 | |
Ornithine Transcarbamylase Deficiency | Hypoglycemia | ORPHA:664 | |
Combined Oxidative Phosphorylation Deficiency 52 | Hypoglycemia, Death in infancy | OMIM:619386 | |
2-Methylbutyryl-Coa Dehydrogenase Deficiency | Hypoglycemia | OMIM:610006 | |
Hsd10 Mitochondrial Disease | Hypoglycemia | OMIM:300438 | |
Short Chain Acyl-Coa Dehydrogenase Deficiency | Ketotic hypoglycemia | ORPHA:26792 | |
Mitochondrial Complex Iv Deficiency, Nuclear Type 4 | Hypoglycemia | OMIM:619048 | |
Glycogen Storage Disease Iii | Hypoglycemia | OMIM:232400 | |
Mitochondrial Complex I Deficiency, Nuclear Type 19 | Hypoglycemia | OMIM:618241 | |
Mitochondrial Trifunctional Protein Deficiency 2 | Hypoglycemia, Death in infancy, Neonatal death | OMIM:620300 | |
Mitochondrial Complex Iii Deficiency, Nuclear Type 11 | Hypoglycemia | OMIM:620137 | |
2P21 Microdeletion Syndrome | Hypoglycemia | ORPHA:163693 | |
Combined Oxidative Phosphorylation Deficiency 34 | Hypoglycemia | OMIM:617872 | |
Combined Malonic And Methylmalonic Acidemia | Hypoglycemia | ORPHA:289504 | |
Glycogen Storage Disease Due To Glucose-6-Phosphatase Deficiency | Hypoglycemia | ORPHA:364 | |
Pyridoxine-Dependent Epilepsy | Hypoglycemia | ORPHA:3006 | |
Hemochromatosis, Neonatal | Hypoglycemia | OMIM:231100 | |
Congenital Cataracts-Facial Dysmorphism-Neuropathy Syndrome | Hypoglycemia | ORPHA:48431 | |
Mitochondrial Complex Iv Deficiency, Nuclear Type 12 | Hypoglycemia, Death in childhood, Death in infancy, Neonatal death, Death in adolescence, Neonata... | OMIM:619055 | |
Combined Oxidative Phosphorylation Deficiency 47 | Hypoglycemia | OMIM:618958 | |
Glycogen Storage Disease Due To Hepatic Glycogen Synthase Deficiency | Postprandial hyperglycemia, Ketotic hypoglycemia, Glycosuria | ORPHA:2089 | |
Insulinoma | Fasting hyperinsulinemia, Recurrent hypoglycemia, Hyperinsulinemia, Reactive hypoglycemia, Nonket... | ORPHA:97279 | |
Combined Oxidative Phosphorylation Deficiency 36 | Hypoglycemia | OMIM:617950 | |
Glycogen Storage Disease Ixb | Hypoglycemia | OMIM:261750 | |
Mody | Glycosuria, Insulin-resistant diabetes mellitus, Hyperglycemia, Glucose intolerance, Transient ne... | ORPHA:552 | |
Mitochondrial Complex Iii Deficiency, Nuclear Type 5 | Hypoglycemia | OMIM:615160 | |
Mitochondrial Complex V (Atp Synthase) Deficiency, Nuclear Type 5 | Hypoglycemia | OMIM:618120 | |
Glycogen Storage Disease Due To Liver Glycogen Phosphorylase Deficiency | Hypoglycemia | ORPHA:369 | |
Pyruvate Carboxylase Deficiency | Hypoglycemia | OMIM:266150 | |
Mitochondrial Complex I Deficiency, Nuclear Type 20 | Hypoglycemia, Death in childhood, Death in infancy | OMIM:611126 | |
Silver-Russell Syndrome Due To 7P11.2P13 Microduplication | Hypoglycemia | ORPHA:231137 | |
Histidinuria-Renal Tubular Defect Syndrome | Hypoglycemia | ORPHA:2158 | |
Glycogen Storage Disease Ixa1 | Hypoglycemia | OMIM:306000 | |
Glucocorticoid Deficiency 3 | Recurrent hypoglycemia | OMIM:609197 | |
Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Hypoglycemia, Impaired gluconeogenesis, Fasting hypoglycemia | OMIM:261680 | |
Malonyl-Coa Decarboxylase Deficiency | Hypoglycemia | OMIM:248360 | |
Silver-Russell Syndrome 2 | Neonatal hypoglycemia | OMIM:618905 | |
Congenital Hyperinsulinism Due To Hnf4A Deficiency | Glycosuria, Hypoketotic hypoglycemia, Hyperinsulinemia, Hyperinsulinemic hypoglycemia, Fasting hy... | ORPHA:263455 | |
Long Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency | Hypoketotic hypoglycemia, Hypoglycemia | ORPHA:5 | |
Non-Acquired Isolated Growth Hormone Deficiency | Neonatal hypoglycemia | ORPHA:631 | |
Mitochondrial Complex Iv Deficiency, Nuclear Type 3 | Neonatal hypoglycemia, Death in infancy | OMIM:619046 | |
Glycogen Storage Disease Ixc | Hypoglycemia, Fasting hypoglycemia | OMIM:613027 | |
Hypoadrenocorticism, Familial | Hypoglycemia | OMIM:240200 | |
Adrenal Hyperplasia, Congenital, Due To 21-Hydroxylase Deficiency | Hypoglycemia | OMIM:201910 | |
3-Methylglutaconic Aciduria With Deafness, Encephalopathy, And Leigh-Like Syndrome | Hypoglycemia | OMIM:614739 | |
Pyruvate Dehydrogenase E3 Deficiency | Hypoglycemia | ORPHA:2394 | |
Combined Oxidative Phosphorylation Deficiency 10 | Hypoglycemia | OMIM:614702 | |
Temple Syndrome | Type II diabetes mellitus, Recurrent hypoglycemia | ORPHA:254516 | |
Glycogen Storage Disease Ixd | Hypoglycemia | OMIM:300559 | |
Infantile Liver Failure Syndrome 2 | Hypoglycemia | OMIM:616483 | |
Blue Diaper Syndrome | Increased proinsulin:insulin ratio, Recurrent hypoglycemia | ORPHA:94086 | |
Multiple Acyl-Coa Dehydrogenase Deficiency | Glycosuria, Hypoglycemia, Neonatal death | OMIM:231680 | |
Laron Syndrome | Hypoglycemia | ORPHA:633 | |
Congenital Isolated Acth Deficiency | Hypoglycemic seizures, Neonatal hypoglycemia | ORPHA:199296 | |
Autosomal Recessive Hyperinsulinism Due To Kir6.2 Deficiency | Neonatal hypoglycemia, Hyperinsulinemic hypoglycemia, Recurrent hypoglycemia | ORPHA:79644 | |
Long-Olsen-Distelmaier Syndrome | Death in childhood, Hypoglycemia | OMIM:620609 | |
Cholestasis, Progressive Familial Intrahepatic, 5 | Hypoglycemia, Death in infancy | OMIM:617049 | |
Combined Oxidative Phosphorylation Deficiency 41 | Hypoglycemia | OMIM:618838 | |
Aromatic L-Amino Acid Decarboxylase Deficiency | Hypoglycemia | ORPHA:35708 | |
Pyridoxal Phosphate-Responsive Seizures | Hypoglycemia | ORPHA:79096 | |
Primary Microcephaly-Mild Intellectual Disability-Young-Onset Diabetes Syndrome | Diabetes mellitus, Hypoglycemia | ORPHA:391408 | |
Proprotein Convertase 1/3 Deficiency | Hypoinsulinemia, Reactive hypoglycemia | OMIM:600955 | |
Acth Deficiency, Isolated | Fasting hypoglycemia | OMIM:201400 | |
Pituitary Stalk Interruption Syndrome | Hypoglycemia, Death in infancy | ORPHA:95496 | |
Polyendocrine-Polyneuropathy Syndrome | Hypoinsulinemia, Type II diabetes mellitus, Hypoglycemia | ORPHA:453533 | |
Mitochondrial Complex Iv Deficiency, Nuclear Type 23 | Hypoglycemia, Death in infancy | OMIM:620275 | |
Classic Galactosemia | Hypoglycemia | ORPHA:79239 | |
Medium Chain Acyl-Coa Dehydrogenase Deficiency | Hypoglycemia | ORPHA:42 | |
Mitochondrial Complex I Deficiency, Nuclear Type 33 | Hypoglycemia | OMIM:618253 | |
Glucocorticoid Resistance, Generalized | Hypoglycemia | OMIM:615962 | |
Carnitine Palmitoyl Transferase 1A Deficiency | Hypoglycemia | ORPHA:156 | |
Glucocorticoid Deficiency 2 | Hypoglycemia, Recurrent hypoglycemia | OMIM:607398 | |
Neurodevelopmental Disorder, Mitochondrial, With Abnormal Movements And Lactic Acidosis, With Or Without Seizures | Hypoglycemia | OMIM:617710 | |
Cataract-Growth Hormone Deficiency-Sensory Neuropathy-Sensorineural Hearing Loss-Skeletal Dysplasia Syndrome | Fasting hypoglycemia | ORPHA:436174 | |
Houge-Janssens Syndrome 1 | Hypoglycemia | OMIM:616355 | |
Galactokinase Deficiency | Hyperinsulinemia, Hypoglycemia | ORPHA:79237 | |
Carnitine Palmitoyltransferase Ii Deficiency, Infantile | Hypoketotic hypoglycemia | OMIM:600649 | |
Growth Delay Due To Insulin-Like Growth Factor Type 1 Deficiency | Insulin resistance, Hypoglycemia | ORPHA:73272 | |
3-Hydroxyacyl-Coa Dehydrogenase Deficiency | Hypoglycemic seizures, Hypoketotic hypoglycemia | OMIM:231530 | |
Fanconi Renotubular Syndrome 4 With Maturity-Onset Diabetes Of The Young | Diabetes mellitus, Glycosuria, Hypoglycemia | OMIM:616026 | |
Hsd10 Disease, Infantile Type | Hypoglycemia | ORPHA:391428 | |
Mitochondrial Complex Iii Deficiency, Nuclear Type 6 | Hyperglycemia, Hypoglycemia | OMIM:615453 | |
Post-Traumatic Pituitary Deficiency | Hypoglycemia | ORPHA:95619 | |
Pituitary Hormone Deficiency, Combined, 2 | Hypoglycemic seizures, Neonatal hypoglycemia | OMIM:262600 | |
Fructose-1,6-Bisphosphatase Deficiency | Hypoglycemia, Neonatal hypoglycemia, Fasting hypoglycemia | ORPHA:348 | |
Pituitary Hormone Deficiency, Combined, 6 | Neonatal hypoglycemia, Hypoglycemia | OMIM:613986 | |
Solitary Fibrous Tumor | Hypoinsulinemia, Hypoglycemia, Recurrent hypoglycemia | ORPHA:2126 | |
Aica-Ribosiduria Due To Atic Deficiency | Hypoglycemia | OMIM:608688 | |
Carnitine Deficiency, Systemic Primary | Impaired gluconeogenesis, Recurrent hypoglycemia | OMIM:212140 | |
Carnitine-Acylcarnitine Translocase Deficiency | Neonatal hypoglycemia, Hypoglycemia | OMIM:212138 | |
Propionic Acidemia | Hypoglycemia | OMIM:606054 | |
Donohue Syndrome | Postprandial hyperglycemia, Hyperglycemia, Hyperinsulinemia, Fasting hypoglycemia | OMIM:246200 | |
Insulin-Resistance Syndrome Type B | Postprandial hyperglycemia, Insulin resistance, Glycosuria, Insulin-resistant diabetes mellitus, ... | ORPHA:2298 | |
Cog8-Cdg | Hypoglycemia | ORPHA:95428 | |
Timothy Syndrome | Hypoglycemia | OMIM:601005 | |
Smith-Kingsmore Syndrome | Hypoglycemia | OMIM:616638 | |
Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency Of | Hypoglycemia | OMIM:201450 | |
Microcephaly, Short Stature, And Impaired Glucose Metabolism 2 | Recurrent hypoglycemia | OMIM:616817 | |
Maple Syrup Urine Disease, Type Ia | Hypoglycemia | OMIM:248600 | |
Glucocorticoid Deficiency 4 With Or Without Mineralocorticoid Deficiency | Hypoglycemia | OMIM:614736 | |
Polyendocrine-Polyneuropathy Syndrome | Type I diabetes mellitus, Hypoglycemia | OMIM:616113 | |
Bachmann-Bupp Syndrome | Hypoglycemia | OMIM:619075 | |
Hypotonia-Cystinuria Syndrome | Neonatal hypoglycemia | OMIM:606407 | |
Mitochondrial Complex Iv Deficiency, Nuclear Type 22 | Hypoglycemia, Death in infancy | OMIM:619355 | |
Fanconi-Bickel Syndrome | Postprandial hyperglycemia, Glycosuria, Fasting hypoglycemia, Diabetes mellitus, Impaired glucose... | ORPHA:2088 | |
Hyperinsulinism Due To Short Chain 3-Hydroxylacyl-Coa Dehydrogenase Deficiency | Fasting hyperinsulinemia, Hypoketotic hypoglycemia, Hyperinsulinemic hypoglycemia, Hypoglycemic s... | ORPHA:71212 | |
3-Methylcrotonyl-Coa Carboxylase 1 Deficiency | Hypoglycemia | OMIM:210200 | |
Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency Of | Nonketotic hypoglycemia, Death in infancy | OMIM:201475 | |
Immunodeficiency, Common Variable, 10 | Hypoglycemia | OMIM:615577 | |
Carnitine Palmitoyltransferase Ii Deficiency, Lethal Neonatal | Hypoglycemia, Nonketotic hypoglycemia, Death in infancy | OMIM:608836 | |
Basilicata-Akhtar Syndrome | Neonatal hypoglycemia | OMIM:301032 | |
Glucocorticoid Deficiency 1 | Recurrent hypoglycemia | OMIM:202200 | |
Shashi-Pena Syndrome | Hypoglycemia | OMIM:617190 | |
Reni Syndrome | Hypoglycemia | OMIM:617575 | |
Silver-Russell Syndrome Due To A Point Mutation | Hypoglycemia | ORPHA:397590 | |
Pancreatic And Cerebellar Agenesis | Hypoglycemia, Hyperglycemia, Diabetes mellitus, Death in infancy | OMIM:609069 | |
Fructose-1,6-Bisphosphatase Deficiency | Hypoglycemia | OMIM:229700 | |
Silver-Russell Syndrome 1 | Fasting hypoglycemia | OMIM:180860 | |
Tenorio Syndrome | Hypoinsulinemia, Hypoglycemia | OMIM:616260 | |
Methylmalonic Aciduria Due To Methylmalonyl-Coa Mutase Deficiency | Hypoglycemia | OMIM:251000 | |
3-Hydroxy-3-Methylglutaryl-Coa Synthase-2 Deficiency | Hypoglycemia | OMIM:605911 | |
Immunodeficiency 10 | Hypoglycemia | OMIM:612783 | |
D-Glyceric Aciduria | Hypoglycemia | OMIM:220120 | |
Intellectual Developmental Disorder, Autosomal Dominant 45 | Neonatal hypoglycemia | OMIM:617600 | |
3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency | Death in childhood, Hypoglycemia | OMIM:246450 | |
Glutaric Acidemia I | Hypoglycemia | OMIM:231670 | |
Congenital Disorder Of Glycosylation, Type Ig | Hypoglycemia | OMIM:607143 | |
Beta-Ketothiolase Deficiency | Hyperglycemia, Hypoglycemia | ORPHA:134 | |
Congenital Disorder Of Glycosylation, Type Im | Hypoketotic hypoglycemia, Death in infancy | OMIM:610768 | |
Dopamine Beta-Hydroxylase Deficiency | Insulin resistance, Hyperinsulinemia, Hypoglycemia | ORPHA:230 | |
Congenital Disorder Of Glycosylation, Type Iie | Hypoglycemia, Death in infancy | OMIM:608779 | |
Multiple Acyl-Coa Dehydrogenase Deficiency | Hypoglycemia | ORPHA:26791 | |
Cholera | Hypoglycemia, Miscarriage | ORPHA:173 | |
Recurrent Metabolic Encephalomyopathic Crises-Rhabdomyolysis-Cardiac Arrhythmia-Intellectual Disability Syndrome | Hypoglycemic seizures, Hypoglycemia | ORPHA:480864 | |
Intellectual Disability-Macrocephaly-Hypotonia-Behavioral Abnormalities Syndrome | Hypoglycemia | ORPHA:457279 | |
Glycogen Storage Disease Due To Liver Phosphorylase Kinase Deficiency | Hypoglycemia, Fasting hypoglycemia | ORPHA:264580 | |
Carnitine-Acylcarnitine Translocase Deficiency | Hypoketotic hypoglycemia, Fasting hypoglycemia | ORPHA:159 | |
Macrocephaly-Intellectual Disability-Neurodevelopmental Disorder-Small Thorax Syndrome | Neonatal hypoglycemia | ORPHA:457485 | |
Glycogen Storage Disease Due To Liver And Muscle Phosphorylase Kinase Deficiency | Ketotic hypoglycemia, Fasting hypoglycemia, Recurrent hypoglycemia | ORPHA:79240 | |
Combined Oxidative Phosphorylation Deficiency 59 | Ketotic hypoglycemia | OMIM:620646 | |
Rabson-Mendenhall Syndrome | Postprandial hyperglycemia, Insulin resistance, Insulin-resistant diabetes mellitus, Fasting hype... | ORPHA:769 | |
Mirage Syndrome | Hypoglycemia | OMIM:617053 | |
Mitochondrial Complex Iii Deficiency, Nuclear Type 1 | Recurrent hypoglycemia, Hyperglycemia, Hypoglycemia, Neonatal death | OMIM:124000 | |
Neurodevelopmental Disorder With Hypotonia, Dysmorphic Facies, And Skeletal Anomalies, With Or Without Seizures | Hypoglycemia | OMIM:620224 | |
Glycogen Storage Disease Ia | Hypoglycemia, Fasting hypoglycemia | OMIM:232200 | |
Midface Hypoplasia, Obesity, Developmental Delay, And Neonatal Hypotonia | Neonatal hypoglycemia | OMIM:608624 | |
Methylmalonic Aciduria, Cblb Type | Hypoglycemia | OMIM:251110 | |
Combined Oxidative Phosphorylation Defect Type 39 | Neonatal hypoglycemia | ORPHA:565624 | |
Sotos Syndrome | Neonatal hypoglycemia, Glucose intolerance | OMIM:117550 | |
Combined Oxidative Phosphorylation Deficiency 58 | Hypoglycemia | OMIM:620451 | |
Leigh Syndrome | Hypoglycemia | ORPHA:506 | |
Carnitine Palmitoyl Transferase Ii Deficiency, Severe Infantile Form | Hypoketotic hypoglycemia | ORPHA:228305 | |
Combined Oxidative Phosphorylation Deficiency 37 | Hypoglycemia | OMIM:618329 | |
Growth Retardation, Impaired Intellectual Development, Hypotonia, And Hepatopathy | Hypoglycemia | OMIM:617093 | |
Late-Onset Isolated Acth Deficiency | Type I diabetes mellitus, Hypoglycemia | ORPHA:199299 | |
Carnitine Palmitoyltransferase I Deficiency | Hypoketotic hypoglycemia | OMIM:255120 | |
Metabolic Crises, Recurrent, With Rhabdomyolysis, Cardiac Arrhythmias, And Neurodegeneration | Hypoglycemia | OMIM:616878 | |
Cataracts, Growth Hormone Deficiency, Sensory Neuropathy, Sensorineural Hearing Loss, And Skeletal Dysplasia | Hypoglycemia | OMIM:616007 | |
Silver-Russell Syndrome | Insulin resistance, Recurrent hypoglycemia | ORPHA:813 | |
Isolated Complex I Deficiency | Diabetes mellitus, Hypoglycemia | ORPHA:2609 | |
3-Methylcrotonyl-Coa Carboxylase 2 Deficiency | Hypoglycemia | OMIM:210210 | |
Multiple Mitochondrial Dysfunctions Syndrome 7 | Hyperglycemia, Hypoglycemia | OMIM:620423 | |
Congenital Disorder Of Glycosylation With Defective Fucosylation 1 | Hypoglycemia | OMIM:618005 | |
3-Methylglutaconic Aciduria Type 7 | Neonatal hypoglycemia | ORPHA:445038 | |
Congenital Disorder Of Glycosylation, Type Iiaa | Hypoglycemia | OMIM:620454 | |
Congenital Disorder Of Glycosylation, Type It | Hypoglycemia | OMIM:614921 | |
Cerebral Visual Impairment | Neonatal hypoglycemia | ORPHA:447788 | |
Mitochondrial Dna Depletion Syndrome 15 (Hepatocerebral Type) | Hypoglycemia, Death in infancy | OMIM:617156 | |
Mitochondrial Trifunctional Protein Deficiency 1 | Hypoketotic hypoglycemia | OMIM:609015 | |
Oculodentodigital Dysplasia | Hypoglycemia | ORPHA:2710 | |
Acyl-Coa Dehydrogenase 9 Deficiency | Nonketotic hypoglycemia | ORPHA:99901 | |
Mitochondrial Dna Depletion Syndrome 3 (Hepatocerebral Type) | Hypoglycemia | OMIM:251880 | |
Carbonic Anhydrase Va Deficiency, Hyperammonemia Due To | Hypoglycemia | OMIM:615751 | |
X-Linked Dominant Chondrodysplasia Punctata | Neonatal hypoglycemia | ORPHA:35173 | |
Immunodeficiency 59 And Hypoglycemia | Hypoglycemia | OMIM:233600 | |
Fanconi-Bickel Syndrome | Postprandial hyperglycemia, Glycosuria, Fasting hypoglycemia | OMIM:227810 | |
Familial Glucocorticoid Deficiency | Hypoglycemic seizures, Ketotic hypoglycemia | ORPHA:361 | |
Pituitary Apoplexy | Hypoglycemia | ORPHA:95613 | |
3-Methylglutaconic Aciduria, Type Viib | Neonatal hypoglycemia | OMIM:616271 | |
3-Methylglutaconic Aciduria, Type Viii | Neonatal hypoglycemia, Death in infancy, Neonatal death | OMIM:617248 | |
Mitochondrial Dna Depletion Syndrome 6 (Hepatocerebral Type) | Hypoglycemia, Recurrent hypoglycemia | OMIM:256810 | |
Orthostatic Hypotension 1 | Neonatal hypoglycemia | OMIM:223360 | |
Bannayan-Riley-Ruvalcaba Syndrome | Hypoglycemia | ORPHA:109 | |
Dilated Cardiomyopathy With Ataxia | Neonatal hypoglycemia | ORPHA:66634 | |
3-Hydroxy-3-Methylglutaric Aciduria | Nonketotic hypoglycemia, Recurrent hypoglycemia | ORPHA:20 | |
Pyruvate Carboxylase Deficiency | Hyperglycemia, Hypoglycemia | ORPHA:3008 | |
Neurodevelopmental Disorder With Hypotonia, Craniofacial Abnormalities, And Seizures | Hypoglycemia | OMIM:614501 | |
Neurologic, Endocrine, And Pancreatic Disease, Multisystem, Infantile-Onset 2 | Neonatal hypoglycemia, Hypoglycemia | OMIM:619418 | |
Wars2-Related Combined Oxidative Phosphorylation Defect | Neonatal hypoglycemia | ORPHA:572798 | |
Mitochondrial Complex I Deficiency, Nuclear Type 1 | Hypoglycemia, Death in infancy | OMIM:252010 | |
Congenital Syphilis | Hypoglycemia | ORPHA:499009 | |
Very Long Chain Acyl-Coa Dehydrogenase Deficiency | Hypoketotic hypoglycemia | ORPHA:26793 | |
Mitochondrial Trifunctional Protein Deficiency | Hypoketotic hypoglycemia | ORPHA:746 | |
Congenital Lipoid Adrenal Hyperplasia Due To Star Deficency | Hypoglycemia | ORPHA:90790 | |
Holoprosencephaly | Diabetes mellitus, Hypoglycemia | ORPHA:2162 | |
Kabuki Syndrome 2 | Neonatal hypoglycemia | OMIM:300867 | |
Shigellosis | Hypoglycemia | ORPHA:810 | |
Sheehan Syndrome | Hypoglycemia | ORPHA:91355 | |
Deeah Syndrome | Death in adolescence, Neonatal hypoglycemia, Death in childhood, Death in infancy | OMIM:619004 | |
Fatal Infantile Lactic Acidosis With Methylmalonic Aciduria | Hypoglycemia | ORPHA:17 | |
Alg12-Cdg | Recurrent hypoglycemia | ORPHA:79324 | |
Glutaryl-Coa Dehydrogenase Deficiency | Fasting hypoglycemia | ORPHA:25 | |
Intellectual Developmental Disorder, X-Linked, Syndromic, With Pigmentary Mosaicism And Coarse Facies | Hypoglycemia | OMIM:301066 | |
Glycogen Storage Disease Ib | Hypoglycemia | OMIM:232220 | |
Multiple Endocrine Neoplasia, Type I | Hypoglycemia | OMIM:131100 | |
Methylmalonic Acidemia With Homocystinuria, Type Cblc | Hypoglycemia | ORPHA:79282 | |
Congenital Adrenal Hyperplasia Due To 3-Beta-Hydroxysteroid Dehydrogenase Deficiency | Neonatal hypoglycemia | ORPHA:90791 | |
Silver-Russell Syndrome Due To Maternal Uniparental Disomy Of Chromosome 7 | Insulin resistance, Fasting hypoglycemia | ORPHA:96182 | |
Acute Adrenal Insufficiency | Hypoglycemia | ORPHA:95409 | |
Carnitine Palmitoyltransferase Ii Deficiency | Hypoketotic hypoglycemia | ORPHA:157 | |
Glycogen Storage Disease Due To Glucose-6-Phosphatase Deficiency Type Ib | Hypoglycemic seizures, Hypoglycemia | ORPHA:79259 | |
Renal Agenesis, Bilateral | Nonketotic hypoglycemia | ORPHA:1848 | |
Perlman Syndrome | Hypoglycemia | OMIM:267000 | |
Simpson-Golabi-Behmel Syndrome | Hypoglycemia, Death in infancy | ORPHA:373 | |
Histiocytoid Cardiomyopathy | Hypoglycemia | ORPHA:137675 | |
Carnitine Palmitoyl Transferase Ii Deficiency, Neonatal Form | Hypoketotic hypoglycemia | ORPHA:228308 | |
Menkes Disease | Hypoglycemia | ORPHA:565 | |
Leprechaunism | Postprandial hyperglycemia, Insulin resistance, Hyperinsulinemia, Recurrent infantile hypoglycemi... | ORPHA:508 | |
Addison Disease | Type I diabetes mellitus, Hypoglycemia | ORPHA:85138 | |
Hereditary Fructose Intolerance | Reactive hypoglycemia | ORPHA:469 | |
Generalized Glucocorticoid Resistance Syndrome | Hypoglycemia | ORPHA:786 | |
Glycogen Storage Disease Ic | Hypoglycemia | OMIM:232240 | |
Deficiency In Anterior Pituitary Function-Variable Immunodeficiency Syndrome | Recurrent hypoglycemia | ORPHA:293978 | |
Tyrosinemia, Type I | Hypoglycemia | OMIM:276700 | |
Rajab Interstitial Lung Disease With Brain Calcifications 1 | Hypoglycemia | OMIM:613658 | |
Glycerol Kinase Deficiency | Hypoglycemia | OMIM:307030 | |
Hypothyroidism Due To Deficient Transcription Factors Involved In Pituitary Development Or Function | Hypoglycemia | ORPHA:226307 | |
Mitochondrial Complex Iv Deficiency, Nuclear Type 5 | Hypoglycemia, Hyperglycemia, Death in infancy | OMIM:220111 | |
Fructose Intolerance, Hereditary | Glycosuria, Hypoglycemia | OMIM:229600 | |
Primary Fanconi Renotubular Syndrome | Glycosuria, Hypoglycemia | ORPHA:3337 | |
Glycogen Storage Disease Of Heart, Lethal Congenital | Neonatal hypoglycemia | OMIM:261740 | |
46,Xy Difference Of Sex Development-Adrenal Insufficiency Due To Cyp11A1 Deficiency | Neonatal hypoglycemia | ORPHA:168558 | |
Inherited Isolated Adrenal Insufficiency Due To Partial Cyp11A1 Deficiency | Neonatal hypoglycemia | ORPHA:289548 | |
Beckwith-Wiedemann Syndrome | Neonatal hypoglycemia, Hypoglycemia | ORPHA:116 | |
Costello Syndrome | Hypoglycemia | OMIM:218040 | |
Marburg Hemorrhagic Fever | Hypoglycemia | ORPHA:99826 | |
Neurooculorenal Syndrome | Recurrent hypoglycemia | OMIM:620305 | |
Megalencephaly-Severe Kyphoscoliosis-Overgrowth Syndrome | Neonatal hypoglycemia | ORPHA:457359 | |
Acute Liver Failure | Hypoglycemia | ORPHA:90062 | |
Non-Acquired Panhypopituitarism | Hypoglycemia | ORPHA:90695 | |
Classic Congenital Adrenal Hyperplasia Due To 21-Hydroxylase Deficiency | Neonatal hypoglycemia, Miscarriage | ORPHA:90794 | |
Holoprosencephaly 1 | Hypoglycemia | OMIM:236100 | |
Combined Pituitary Hormone Deficiencies, Genetic Forms | Hypoglycemia | ORPHA:95494 | |
Antley-Bixler Syndrome With Genital Anomalies And Disordered Steroidogenesis | Hypoglycemia | OMIM:201750 | |
Beckwith-Wiedemann Syndrome | Neonatal hypoglycemia | OMIM:130650 | |
Sotos Syndrome | Neonatal hypoglycemia | ORPHA:821 |
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MGI Allele | Allele Type | Produced |
---|---|---|
Gga2tm1e(EUCOMM)Hmgu | Targeted, non-conditional allele | ES Cells |
Gga2tm1a(EUCOMM)Hmgu | KO first allele (reporter-tagged insertion with conditional potential) | Targeting vectors, ES Cells |
Gga2em1(IMPC)Ccpcz | Exon Deletion | Mice |
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