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Gene: Gga2 MGI:1921355

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Not currently registered for phenotyping at IMPC

Phenotyping is currently not planned for a knockout strain of this gene.

Gene Summary

Name:
golgi associated, gamma adaptin ear containing, ARF binding protein 2
Synonyms:
1200007E24Rik

Order Alleles

IMPC Data Collections

  • No Body Weight Data
  • No Embryo Imaging Data
  • No Viability Data

IMPC Phenotype Summary

Significant
Not Significant
Not tested

View all our phenotype data below

Phenotypes

The IMPC applies a panel of phenotyping screens to characterise single-gene knockout mice by comparison to wild types. Click on the different tabs to visualise significant phenotypes identified by the IMPC, as well as all data that was measured.

lacZ Expression

Expression data not available

Associated Images

Images submitted by IMPC centres for a selection of procedures. Each set of images is available to view in our image comparator.

Phenotype associated images not available

Human diseases caused by Gga2 mutations

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.

No human diseases associated to this gene by orthology or annotation.

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
Hyperinsulinemic Hypoglycemia, Familial, 7
Hyperinsulinemia, Hypoglycemia, Hypoglycemic seizures, Hyperinsulinemic hypoglycemia OMIM:610021
3-Hydroxy-3-Methylglutaryl-Coa Synthase Deficiency
Hypoglycemia ORPHA:35701
Glycogen Storage Disease 0, Liver
Postprandial hyperglycemia, Neonatal hypoglycemia, Fasting hypoglycemia OMIM:240600
Glucocorticoid Deficiency 3
Recurrent hypoglycemia OMIM:609197
Hyperinsulinism Due To Insr Deficiency
Hypoglycemia, Insulin resistance, 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
Congenital Glucokinase-Related Hyperinsulinism
Fasting hyperinsulinemia, Recurrent hypoglycemia, Type II diabetes mellitus, Hyperinsulinemic hyp... ORPHA:79299
Hyperinsulinemic Hypoglycemia, Familial, 2
Hypoglycemia, Hyperinsulinemic hypoglycemia OMIM:601820
Hypoinsulinemic Hypoglycemia With Hemihypertrophy
Neonatal hypoglycemia, Hypoglycemia, Hypoinsulinemia, Fasting hypoglycemia OMIM:240900
Insulin Autoimmune Syndrome
Nonketotic hypoglycemia, Reactive hypoglycemia, Insulin-resistant diabetes mellitus, Insulin resi... ORPHA:411593
Short Stature Due To Partial Ghr Deficiency
Hypoglycemia ORPHA:314802
Phosphoenolpyruvate Carboxykinase Deficiency, Mitochondrial
Impaired gluconeogenesis, Hypoglycemia OMIM:261650
Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency
Hypoglycemia OMIM:609016
Hypoglycemia, Leucine-Induced
Hypoglycemia, Hyperinsulinemic hypoglycemia OMIM:240800
Glycogen Storage Disease Due To Glycogen Debranching Enzyme Deficiency
Hypoglycemia ORPHA:366
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
Ketotic hypoglycemia, Maternal diabetes, Reactive hypoglycemia, Maturity-onset diabetes of the yo... ORPHA:324575
Hernia, Anterior Diaphragmatic
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, Fasting hyperinsulinemia, Reactive hypoglycemia ORPHA:35878
Hypoinsulinemic Hypoglycemia And Body Hemihypertrophy
Nonketotic hypoglycemia, Neonatal hypoglycemia, Hypoglycemic seizures, Hypoketotic hypoglycemia ORPHA:293964
Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, And Somatic Abnormalities
Hypoglycemia, Insulin-resistant diabetes mellitus, Hyperinsulinemia, Diabetic ketoacidosis, Fasti... OMIM:262190
Non-Insulinoma Pancreatogenous Hypoglycemia Syndrome
Reactive hypoglycemia, Hyperinsulinemia, Fasting hypoglycemia, Hyperinsulinemic hypoglycemia, Hyp... 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
Autosomal Dominant Hyperinsulinism Due To Kir6.2 Deficiency
Maternal diabetes, Hyperinsulinemia, Hypoglycemic seizures, Fasting hypoglycemia, Hyperinsulinemi... ORPHA:276580
Neutropenia, Lethal Congenital, With Eosinophilia
Neonatal death OMIM:257100
Hyperinsulinemic Hypoglycemia, Familial, 8
Hyperinsulinemia, Hypoglycemia, Hypoglycemic seizures OMIM:620211
Dicarboxylic Aminoaciduria
Fasting hypoglycemia OMIM:222730
Endocardial Fibroelastosis
Hypoglycemia ORPHA:2022
Dihydrolipoamide Dehydrogenase Deficiency
Hypoglycemia, Death in childhood OMIM:246900
Mitochondrial Complex Iii Deficiency, Nuclear Type 9
Hypoglycemia OMIM:616111
Hyperinsulinism Due To Ucp2 Deficiency
Reactive hypoglycemia, Hypoglycemic seizures, Recurrent hypoglycemia, Hyperinsulinemic hypoglycem... ORPHA:276556
Combined Oxidative Phosphorylation Deficiency 40
Neonatal death, Death in infancy, Hypoglycemia OMIM:618835
Combined Oxidative Phosphorylation Deficiency 42
Neonatal death, Death in infancy, Hypoglycemia OMIM:618839
Autosomal Dominant Hyperinsulinism Due To Sur1 Deficiency
Hyperinsulinemia, Hypoglycemic seizures, Fasting hypoglycemia, Hyperinsulinemic hypoglycemia, Typ... ORPHA:276575
Orthostatic Hypotension 2
Hypoglycemia OMIM:618182
Diarrhea 13
Recurrent hypoglycemia OMIM:620357
Mitochondrial Dna Depletion Syndrome 9 (Encephalomyopathic Type With Methylmalonic Aciduria)
Neonatal death, Death in infancy, Hypoglycemia, Death in childhood 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
Hypoglycemia, Neonatal hypoglycemia ORPHA:231140
Mitochondrial Pyruvate Carrier Deficiency
Hypoglycemia OMIM:614741
3-Methylglutaconic Aciduria Type 4
Hypoglycemia ORPHA:67048
Silver-Russell Syndrome Due To Maternal Uniparental Disomy Of Chromosome 11
Hypoglycemia ORPHA:231147
Isobutyryl-Coa Dehydrogenase Deficiency
Ketotic hypoglycemia ORPHA:79159
Intellectual Developmental Disorder With Macrocephaly, Seizures, And Speech Delay
Recurrent hypoglycemia OMIM:618158
Mehmo Syndrome
Hypoglycemia OMIM:300148
Riboflavin Deficiency
Hypoglycemia OMIM:615026
Ornithine Transcarbamylase Deficiency
Hypoglycemia ORPHA:664
Monocarboxylate Transporter 1 Deficiency
Ketotic hypoglycemia OMIM:616095
Combined Oxidative Phosphorylation Deficiency 52
Death in infancy, Hypoglycemia OMIM:619386
2-Methylbutyryl-Coa Dehydrogenase Deficiency
Hypoglycemia OMIM:610006
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
Glucocorticoid Deficiency 2
Recurrent hypoglycemia OMIM:607398
Mitochondrial Complex I Deficiency, Nuclear Type 19
Hypoglycemia OMIM:618241
Mitochondrial Trifunctional Protein Deficiency 2
Neonatal death, Death in infancy, Hypoglycemia OMIM:620300
2P21 Microdeletion Syndrome
Hypoglycemia ORPHA:163693
Mitochondrial Complex Iii Deficiency, Nuclear Type 11
Hypoglycemia OMIM:620137
Hsd10 Mitochondrial Disease
Hypoglycemia OMIM:300438
Combined Malonic And Methylmalonic Acidemia
Hypoglycemia ORPHA:289504
Congenital Cataracts-Facial Dysmorphism-Neuropathy Syndrome
Hypoglycemia ORPHA:48431
Combined Oxidative Phosphorylation Deficiency 34
Hypoglycemia OMIM:617872
Pyridoxine-Dependent Epilepsy
Hypoglycemia ORPHA:3006
Glycogen Storage Disease Due To Glucose-6-Phosphatase Deficiency
Hypoglycemia ORPHA:364
Mitochondrial Complex Iv Deficiency, Nuclear Type 12
Death in infancy, Hypoglycemia, Death in adolescence, Death in childhood, Neonatal death, Neonata... OMIM:619055
Glycogen Storage Disease Ixb
Hypoglycemia OMIM:261750
Insulinoma
Nonketotic hypoglycemia, Reactive hypoglycemia, Fasting hyperinsulinemia, Hyperinsulinemia, Recur... ORPHA:97279
Combined Oxidative Phosphorylation Deficiency 47
Hypoglycemia OMIM:618958
Glycogen Storage Disease Due To Hepatic Glycogen Synthase Deficiency
Postprandial hyperglycemia, Ketotic hypoglycemia, Glycosuria ORPHA:2089
Combined Oxidative Phosphorylation Deficiency 36
Hypoglycemia OMIM:617950
Hemochromatosis, Neonatal
Hypoglycemia OMIM:231100
Mody
Transient neonatal diabetes mellitus, Insulin-resistant diabetes mellitus, Diabetic ketoacidosis,... ORPHA:552
Mitochondrial Complex Iii Deficiency, Nuclear Type 5
Hypoglycemia OMIM:615160
Glycogen Storage Disease Ixa1
Hypoglycemia OMIM:306000
Pyruvate Carboxylase Deficiency
Hypoglycemia OMIM:266150
Glycogen Storage Disease Due To Liver Glycogen Phosphorylase Deficiency
Hypoglycemia ORPHA:369
Mitochondrial Complex V (Atp Synthase) Deficiency, Nuclear Type 5
Hypoglycemia OMIM:618120
Adrenal Hyperplasia, Congenital, Due To 21-Hydroxylase Deficiency
Hypoglycemia OMIM:201910
Histidinuria-Renal Tubular Defect Syndrome
Hypoglycemia ORPHA:2158
Mitochondrial Complex I Deficiency, Nuclear Type 20
Death in infancy, Hypoglycemia, Death in childhood OMIM:611126
Silver-Russell Syndrome Due To 7P11.2P13 Microduplication
Hypoglycemia ORPHA:231137
Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic
Impaired gluconeogenesis, Hypoglycemia, Fasting hypoglycemia OMIM:261680
Congenital Hyperinsulinism Due To Hnf4A Deficiency
Hyperinsulinemia, Fasting hypoglycemia, Glycosuria, Hyperinsulinemic hypoglycemia, Neonatal hypog... ORPHA:263455
Malonyl-Coa Decarboxylase Deficiency
Hypoglycemia OMIM:248360
Glycogen Storage Disease Ixc
Hypoglycemia, Fasting hypoglycemia OMIM:613027
Silver-Russell Syndrome 2
Neonatal hypoglycemia OMIM:618905
Hypoadrenocorticism, Familial
Hypoglycemia OMIM:240200
Long Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency
Hypoglycemia, Hypoketotic hypoglycemia ORPHA:5
Glycogen Storage Disease Ixd
Hypoglycemia OMIM:300559
Mitochondrial Complex Iv Deficiency, Nuclear Type 3
Death in infancy, Neonatal hypoglycemia OMIM:619046
Pyridoxal Phosphate-Responsive Seizures
Hypoglycemia ORPHA:79096
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
Recurrent hypoglycemia, Type II diabetes mellitus ORPHA:254516
3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency
Hypoglycemia, Death in childhood OMIM:246450
Cholestasis, Progressive Familial Intrahepatic, 5
Death in infancy, Hypoglycemia OMIM:617049
Infantile Liver Failure Syndrome 2
Hypoglycemia OMIM:616483
Multiple Acyl-Coa Dehydrogenase Deficiency
Neonatal death, Hypoglycemia, Glycosuria OMIM:231680
Blue Diaper Syndrome
Recurrent hypoglycemia, Increased proinsulin:insulin ratio ORPHA:94086
Laron Syndrome
Hypoglycemia ORPHA:633
Proprotein Convertase 1/3 Deficiency
Hypoinsulinemia, Reactive hypoglycemia OMIM:600955
Combined Oxidative Phosphorylation Deficiency 41
Hypoglycemia OMIM:618838
Primary Microcephaly-Mild Intellectual Disability-Young-Onset Diabetes Syndrome
Diabetes mellitus, Hypoglycemia ORPHA:391408
Pituitary Stalk Interruption Syndrome
Death in infancy, Hypoglycemia ORPHA:95496
Acth Deficiency, Isolated
Fasting hypoglycemia OMIM:201400
Polyendocrine-Polyneuropathy Syndrome
Type II diabetes mellitus, Hypoglycemia, Hypoinsulinemia ORPHA:453533
Mitochondrial Complex Iv Deficiency, Nuclear Type 23
Death in infancy, Hypoglycemia OMIM:620275
Autosomal Recessive Hyperinsulinism Due To Kir6.2 Deficiency
Recurrent hypoglycemia, Neonatal hypoglycemia, Hyperinsulinemic hypoglycemia ORPHA:79644
Classic Galactosemia
Hypoglycemia ORPHA:79239
Mitochondrial Complex I Deficiency, Nuclear Type 33
Hypoglycemia OMIM:618253
Carnitine Palmitoyl Transferase 1A Deficiency
Hypoglycemia ORPHA:156
Medium Chain Acyl-Coa Dehydrogenase Deficiency
Hypoglycemia ORPHA:42
Congenital Isolated Acth Deficiency
Neonatal hypoglycemia, Hypoglycemic seizures ORPHA:199296
Glucocorticoid Resistance, Generalized
Hypoglycemia OMIM:615962
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
Neurodevelopmental Disorder, Mitochondrial, With Abnormal Movements And Lactic Acidosis, With Or Without Seizures
Hypoglycemia OMIM:617710
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, Hypoglycemia, Glycosuria OMIM:616026
Hsd10 Disease, Infantile Type
Hypoglycemia ORPHA:391428
Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency Of
Hypoglycemia OMIM:201450
Carnitine Palmitoyltransferase Ii Deficiency, Infantile
Hypoketotic hypoglycemia OMIM:600649
Fructose-1,6-Bisphosphatase Deficiency
Fasting hypoglycemia, Hypoglycemia, Neonatal hypoglycemia ORPHA:348
Post-Traumatic Pituitary Deficiency
Hypoglycemia ORPHA:95619
Pituitary Hormone Deficiency, Combined, 2
Neonatal hypoglycemia, Hypoglycemic seizures OMIM:262600
Mitochondrial Complex Iii Deficiency, Nuclear Type 6
Hyperglycemia, Hypoglycemia OMIM:615453
Pituitary Hormone Deficiency, Combined, 6
Hypoglycemia, Neonatal hypoglycemia OMIM:613986
Solitary Fibrous Tumor
Recurrent hypoglycemia, Hypoglycemia, Hypoinsulinemia ORPHA:2126
Carnitine-Acylcarnitine Translocase Deficiency
Hypoglycemia, Neonatal hypoglycemia OMIM:212138
Carnitine Deficiency, Systemic Primary
Impaired gluconeogenesis, Recurrent hypoglycemia OMIM:212140
Donohue Syndrome
Postprandial hyperglycemia, Hyperglycemia, Hyperinsulinemia, Fasting hypoglycemia OMIM:246200
Propionic Acidemia
Hypoglycemia OMIM:606054
Insulin-Resistance Syndrome Type B
Insulin resistance, Fasting hyperinsulinemia, Insulin-resistant diabetes mellitus, Hyperinsulinem... ORPHA:2298
Maple Syrup Urine Disease
Hypoglycemia OMIM:248600
Cog8-Cdg
Hypoglycemia ORPHA:95428
Smith-Kingsmore Syndrome
Hypoglycemia OMIM:616638
Aica-Ribosuria Due To Atic Deficiency
Hypoglycemia OMIM:608688
Timothy Syndrome
Hypoglycemia OMIM:601005
Microcephaly, Short Stature, And Impaired Glucose Metabolism 2
Recurrent hypoglycemia OMIM:616817
Polyendocrine-Polyneuropathy Syndrome
Type I diabetes mellitus, Hypoglycemia OMIM:616113
Glucocorticoid Deficiency 4 With Or Without Mineralocorticoid Deficiency
Hypoglycemia OMIM:614736
Hypotonia-Cystinuria Syndrome
Neonatal hypoglycemia OMIM:606407
Bachmann-Bupp Syndrome
Hypoglycemia OMIM:619075
Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency Of
Nonketotic hypoglycemia, Death in infancy OMIM:201475
Mitochondrial Complex Iv Deficiency, Nuclear Type 22
Death in infancy, Hypoglycemia OMIM:619355
Fanconi-Bickel Syndrome
Diabetes mellitus, Impaired glucose tolerance, Fasting hypoglycemia, Glycosuria, Postprandial hyp... ORPHA:2088
Hyperinsulinism Due To Short Chain 3-Hydroxylacyl-Coa Dehydrogenase Deficiency
Fasting hyperinsulinemia, Hypoglycemic seizures, Hyperinsulinemic hypoglycemia, Neonatal hypoglyc... ORPHA:71212
3-Methylcrotonyl-Coa Carboxylase 1 Deficiency
Hypoglycemia OMIM:210200
Carnitine Palmitoyltransferase Ii Deficiency, Lethal Neonatal
Nonketotic hypoglycemia, Death in infancy, Hypoglycemia OMIM:608836
Basilicata-Akhtar Syndrome
Neonatal hypoglycemia OMIM:301032
Fructose-1,6-Bisphosphatase Deficiency
Hypoglycemia OMIM:229700
Methylmalonic Aciduria Due To Methylmalonyl-Coa Mutase Deficiency
Hypoglycemia OMIM:251000
Reni Syndrome
Hypoglycemia OMIM:617575
Glucocorticoid Deficiency 1
Recurrent hypoglycemia OMIM:202200
Immunodeficiency, Common Variable, 10
Hypoglycemia OMIM:615577
Silver-Russell Syndrome Due To A Point Mutation
Hypoglycemia ORPHA:397590
Pancreatic And Cerebellar Agenesis
Death in infancy, Hyperglycemia, Diabetes mellitus, Hypoglycemia OMIM:609069
Shashi-Pena Syndrome
Hypoglycemia OMIM:617190
Tenorio Syndrome
Hypoglycemia, Hypoinsulinemia OMIM:616260
D-Glyceric Aciduria
Hypoglycemia OMIM:220120
Silver-Russell Syndrome 1
Fasting hypoglycemia OMIM:180860
Intellectual Developmental Disorder, Autosomal Dominant 45
Neonatal hypoglycemia OMIM:617600
Carnitine Palmitoyltransferase I Deficiency
Hypoketotic hypoglycemia OMIM:255120
Congenital Disorder Of Glycosylation, Type Ig
Hypoglycemia OMIM:607143
Glutaric Acidemia I
Hypoglycemia OMIM:231670
Dopamine Beta-Hydroxylase Deficiency
Insulin resistance, Hyperinsulinemia, Hypoglycemia ORPHA:230
Congenital Disorder Of Glycosylation, Type Im
Death in infancy, Hypoketotic hypoglycemia OMIM:610768
Beta-Ketothiolase Deficiency
Hyperglycemia, Hypoglycemia ORPHA:134
Multiple Acyl-Coa Dehydrogenase Deficiency
Hypoglycemia ORPHA:26791
Congenital Disorder Of Glycosylation, Type Iie
Death in infancy, Hypoglycemia OMIM:608779
Cholera
Miscarriage, Hypoglycemia ORPHA:173
Recurrent Metabolic Encephalomyopathic Crises-Rhabdomyolysis-Cardiac Arrhythmia-Intellectual Disability Syndrome
Hypoglycemia, Hypoglycemic seizures 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
Glycogen Storage Disease Due To Liver And Muscle Phosphorylase Kinase Deficiency
Recurrent hypoglycemia, Ketotic hypoglycemia, Fasting hypoglycemia ORPHA:79240
Carnitine-Acylcarnitine Translocase Deficiency
Fasting hypoglycemia, Hypoketotic hypoglycemia ORPHA:159
Macrocephaly-Intellectual Disability-Neurodevelopmental Disorder-Small Thorax Syndrome
Neonatal hypoglycemia ORPHA:457485
Rabson-Mendenhall Syndrome
Impaired glucose tolerance, Insulin resistance, Fasting hyperinsulinemia, Insulin-resistant diabe... ORPHA:769
Mitochondrial Complex Iii Deficiency, Nuclear Type 1
Neonatal death, Recurrent hypoglycemia, Hypoglycemia, Hyperglycemia OMIM:124000
Neurodevelopmental Disorder With Hypotonia, Dysmorphic Facies, And Skeletal Anomalies, With Or Without Seizures
Hypoglycemia OMIM:620224
Mirage Syndrome
Hypoglycemia OMIM:617053
Glycogen Storage Disease Ia
Hypoglycemia, Fasting hypoglycemia OMIM:232200
Combined Oxidative Phosphorylation Defect Type 39
Neonatal hypoglycemia ORPHA:565624
Midface Hypoplasia, Obesity, Developmental Delay, And Neonatal Hypotonia
Neonatal hypoglycemia OMIM:608624
Leigh Syndrome
Hypoglycemia ORPHA:506
Sotos Syndrome
Glucose intolerance, Neonatal hypoglycemia OMIM:117550
3-Methylcrotonyl-Coa Carboxylase 2 Deficiency
Hypoglycemia OMIM:210210
Combined Oxidative Phosphorylation Deficiency 37
Hypoglycemia OMIM:618329
Carnitine Palmitoyl Transferase Ii Deficiency, Severe Infantile Form
Hypoketotic hypoglycemia ORPHA:228305
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
Growth Retardation, Impaired Intellectual Development, Hypotonia, And Hepatopathy
Hypoglycemia OMIM:617093
Mitochondrial Dna Depletion Syndrome 3 (Hepatocerebral Type)
Hypoglycemia OMIM:251880
Late-Onset Isolated Acth Deficiency
Type I diabetes mellitus, Hypoglycemia ORPHA:199299
Congenital Disorder Of Glycosylation With Defective Fucosylation 1
Hypoglycemia OMIM:618005
Congenital Disorder Of Glycosylation, Type It
Hypoglycemia OMIM:614921
3-Methylglutaconic Aciduria Type 7
Neonatal hypoglycemia ORPHA:445038
Isolated Complex I Deficiency
Diabetes mellitus, Hypoglycemia ORPHA:2609
Cerebral Visual Impairment
Neonatal hypoglycemia ORPHA:447788
Mitochondrial Dna Depletion Syndrome 15 (Hepatocerebral Type)
Death in infancy, Hypoglycemia OMIM:617156
Mitochondrial Trifunctional Protein Deficiency 1
Hypoketotic hypoglycemia OMIM:609015
Oculodentodigital Dysplasia
Hypoglycemia ORPHA:2710
Orthostatic Hypotension 1
Neonatal hypoglycemia OMIM:223360
Carbonic Anhydrase Va Deficiency, Hyperammonemia Due To
Hypoglycemia OMIM:615751
Acyl-Coa Dehydrogenase 9 Deficiency
Nonketotic hypoglycemia ORPHA:99901
X-Linked Dominant Chondrodysplasia Punctata
Neonatal hypoglycemia ORPHA:35173
Immunodeficiency 59 And Hypoglycemia
Hypoglycemia OMIM:233600
Pituitary Apoplexy
Hypoglycemia ORPHA:95613
Fanconi-Bickel Syndrome
Postprandial hyperglycemia, Fasting hypoglycemia, Glycosuria OMIM:227810
3-Methylglutaconic Aciduria, Type Viii
Neonatal death, Death in infancy, Neonatal hypoglycemia OMIM:617248
Familial Glucocorticoid Deficiency
Ketotic hypoglycemia, Hypoglycemic seizures ORPHA:361
3-Methylglutaconic Aciduria, Type Viib
Neonatal hypoglycemia OMIM:616271
Mitochondrial Dna Depletion Syndrome 6 (Hepatocerebral Type)
Recurrent hypoglycemia, Hypoglycemia OMIM:256810
Bannayan-Riley-Ruvalcaba Syndrome
Hypoglycemia ORPHA:109
Dilated Cardiomyopathy With Ataxia
Neonatal hypoglycemia ORPHA:66634
Neurodevelopmental Disorder With Hypotonia, Craniofacial Abnormalities, And Seizures
Hypoglycemia OMIM:614501
3-Hydroxy-3-Methylglutaric Aciduria
Nonketotic hypoglycemia, Recurrent hypoglycemia ORPHA:20
Wars2-Related Combined Oxidative Phosphorylation Defect
Neonatal hypoglycemia ORPHA:572798
Neurologic, Endocrine, And Pancreatic Disease, Multisystem, Infantile-Onset 2
Hypoglycemia, Neonatal hypoglycemia OMIM:619418
Pyruvate Carboxylase Deficiency
Hyperglycemia, Hypoglycemia ORPHA:3008
Mitochondrial Trifunctional Protein Deficiency
Hypoketotic hypoglycemia ORPHA:746
Very Long Chain Acyl-Coa Dehydrogenase Deficiency
Hypoketotic hypoglycemia ORPHA:26793
Mitochondrial Complex I Deficiency, Nuclear Type 1
Death in infancy, Hypoglycemia OMIM:252010
Congenital Lipoid Adrenal Hyperplasia Due To Star Deficency
Hypoglycemia ORPHA:90790
Holoprosencephaly
Diabetes mellitus, Hypoglycemia ORPHA:2162
Kabuki Syndrome 2
Neonatal hypoglycemia OMIM:300867
Sheehan Syndrome
Hypoglycemia ORPHA:91355
Shigellosis
Hypoglycemia ORPHA:810
Fatal Infantile Lactic Acidosis With Methylmalonic Aciduria
Hypoglycemia ORPHA:17
Deeah Syndrome
Death in infancy, Death in adolescence, Neonatal hypoglycemia, Death in childhood OMIM:619004
Alg12-Cdg
Recurrent hypoglycemia ORPHA:79324
Glycogen Storage Disease Ib
Hypoglycemia OMIM:232220
Glutaryl-Coa Dehydrogenase Deficiency
Fasting hypoglycemia ORPHA:25
Intellectual Developmental Disorder, X-Linked, Syndromic, With Pigmentary Mosaicism And Coarse Facies
Hypoglycemia OMIM:301066
Methylmalonic Acidemia With Homocystinuria, Type Cblc
Hypoglycemia ORPHA:79282
Congenital Adrenal Hyperplasia Due To 3-Beta-Hydroxysteroid Dehydrogenase Deficiency
Neonatal hypoglycemia ORPHA:90791
Multiple Endocrine Neoplasia, Type I
Hypoglycemia OMIM:131100
Acute Adrenal Insufficiency
Hypoglycemia ORPHA:95409
Silver-Russell Syndrome Due To Maternal Uniparental Disomy Of Chromosome 7
Insulin resistance, Fasting hypoglycemia ORPHA:96182
Carnitine Palmitoyltransferase Ii Deficiency
Hypoketotic hypoglycemia ORPHA:157
Glycogen Storage Disease Due To Glucose-6-Phosphatase Deficiency Type Ib
Hypoglycemia, Hypoglycemic seizures ORPHA:79259
Perlman Syndrome
Hypoglycemia OMIM:267000
Renal Agenesis, Bilateral
Nonketotic hypoglycemia ORPHA:1848
Simpson-Golabi-Behmel Syndrome
Death in infancy, Hypoglycemia ORPHA:373
Histiocytoid Cardiomyopathy
Hypoglycemia ORPHA:137675
Carnitine Palmitoyl Transferase Ii Deficiency, Neonatal Form
Hypoketotic hypoglycemia ORPHA:228308
Menkes Disease
Hypoglycemia ORPHA:565
Leprechaunism
Insulin resistance, Hyperinsulinemia, Recurrent infantile hypoglycemia, Fasting hypoglycemia, Pos... 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
Glycerol Kinase Deficiency
Hypoglycemia OMIM:307030
Tyrosinemia, Type I
Hypoglycemia OMIM:276700
Glycogen Storage Disease Ic
Hypoglycemia OMIM:232240
Mitochondrial Complex Iv Deficiency, Nuclear Type 5
Death in infancy, Hyperglycemia, Hypoglycemia OMIM:220111
Hypothyroidism Due To Deficient Transcription Factors Involved In Pituitary Development Or Function
Hypoglycemia ORPHA:226307
Deficiency In Anterior Pituitary Function-Variable Immunodeficiency Syndrome
Recurrent hypoglycemia ORPHA:293978
Fructose Intolerance, Hereditary
Hypoglycemia, Glycosuria OMIM:229600
Primary Fanconi Renotubular Syndrome
Hypoglycemia, Glycosuria ORPHA:3337
Rajab Interstitial Lung Disease With Brain Calcifications 1
Hypoglycemia OMIM:613658
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
Glycogen Storage Disease Of Heart, Lethal Congenital
Neonatal hypoglycemia OMIM:261740
Beckwith-Wiedemann Syndrome
Hypoglycemia, Neonatal hypoglycemia ORPHA:116
Costello Syndrome
Hypoglycemia OMIM:218040
Marburg Hemorrhagic Fever
Hypoglycemia ORPHA:99826
Megalencephaly-Severe Kyphoscoliosis-Overgrowth Syndrome
Neonatal hypoglycemia ORPHA:457359
Neurooculorenal Syndrome
Recurrent hypoglycemia OMIM:620305
Acute Liver Failure
Hypoglycemia ORPHA:90062
Classic Congenital Adrenal Hyperplasia Due To 21-Hydroxylase Deficiency
Miscarriage, Neonatal hypoglycemia ORPHA:90794
Non-Acquired Panhypopituitarism
Hypoglycemia ORPHA:90695
Holoprosencephaly 1
Hypoglycemia OMIM:236100
Antley-Bixler Syndrome With Genital Anomalies And Disordered Steroidogenesis
Hypoglycemia OMIM:201750
Beckwith-Wiedemann Syndrome
Neonatal hypoglycemia OMIM:130650
Combined Pituitary Hormone Deficiencies, Genetic Forms
Hypoglycemia ORPHA:95494
Sotos Syndrome
Neonatal hypoglycemia ORPHA:821

Histopathology

Summary table of phenotypes displayed during the Histopathology procedure which are considered significant. Full histopathology data table, including submitted images, can be accessed by clicking any row in this table.

There is no histopathology data for Gga2

IMPC related publications

The table below lists publications which used either products generated by the IMPC or data produced by the phenotyping efforts of the IMPC. These publications have also been associated to Gga2.

No publications found that use IMPC mice or data for Gga2.

Order Mouse and ES Cells

All available products are supplied via our member's centres or partnerships. When ordering a product from the IMPC you will be redirected to one of their websites or prompted to start an email.

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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