Gene Summary
IMPC Data Collections
- Body Weight Measurements
- No Embryo Imaging Data
- Viability Data
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.
An assay measuring the expression of lacZ shows the tissue where the gene is expressed.
Anatomy | Images | Zygosity | Mutant Expr |
---|---|---|---|
Adrenal gland | Section images | heterozygote | 100% (2 of 2) |
Aorta | Section images | heterozygote | 100% (2 of 2) |
Brain | Section images | heterozygote | 100% (2 of 2) |
Brainstem | Section images | heterozygote | 100% (2 of 2) |
Cartilage tissue | Section images | heterozygote | 100% (2 of 2) |
Cerebellum | Section images | heterozygote | 100% (2 of 2) |
Cerebral cortex | Section images | heterozygote | 100% (2 of 2) |
Epididymis | Section images | heterozygote | 50% (1 of 2) |
Eye | Section images | heterozygote | 100% (2 of 2) |
Heart | Section images | heterozygote | 100% (2 of 2) |
Hippocampus | Section images | heterozygote | 100% (2 of 2) |
Hypothalamus | Section images | heterozygote | 100% (2 of 2) |
Kidney | Section images | heterozygote | 100% (2 of 2) |
Large intestine | Section images | heterozygote | 100% (2 of 2) |
Lung | Section images | heterozygote | 100% (2 of 2) |
Midbrain | Section images | heterozygote | 100% (2 of 2) |
Olfactory lobe | Section images | heterozygote | 100% (2 of 2) |
Ovary | Section images | heterozygote | 50% (1 of 2) |
Oviduct | Section images | heterozygote | 50% (1 of 2) |
Pancreas | Section images | heterozygote | 100% (2 of 2) |
Pituitary gland | Section images | heterozygote | 100% (2 of 2) |
Skin | Section images | heterozygote | 100% (2 of 2) |
Small intestine | Section images | heterozygote | 100% (2 of 2) |
Spinal cord | Section images | heterozygote | 100% (2 of 2) |
Stomach | Section images | heterozygote | 100% (2 of 2) |
Submandibular gland | Section images | heterozygote | 50% (1 of 2) |
Testis | Section images | heterozygote | 50% (1 of 2) |
Thalamus | Section images | heterozygote | 100% (2 of 2) |
Thymus | Section images | heterozygote | 50% (1 of 2) |
Thyroid gland | Section images | heterozygote | Ambiguous |
Trachea | Section images | heterozygote | 100% (2 of 2) |
Uterus | Section images | heterozygote | 50% (1 of 2) |
Brown adipose tissue | N/A | heterozygote | 0.0% (0 of 2) |
Esophagus | N/A | heterozygote | 0.0% (0 of 2) |
Liver | N/A | heterozygote | 0.0% (0 of 2) |
Lower urinary tract | N/A | heterozygote | Not available |
Lymph node | N/A | heterozygote | 0.0% (0 of 2) |
Mammary gland | N/A | heterozygote | 0.0% (0 of 2) |
Peripheral nervous system | N/A | heterozygote | 0.0% (0 of 2) |
Peyer's patch | N/A | heterozygote | 0.0% (0 of 2) |
Prostate gland | N/A | heterozygote | Not available |
Skeletal muscle | N/A | heterozygote | 0.0% (0 of 2) |
Spleen | N/A | heterozygote | 0.0% (0 of 2) |
Striatum | N/A | heterozygote | 0.0% (0 of 2) |
Urinary bladder | N/A | heterozygote | 0.0% (0 of 2) |
Vascular system | N/A | heterozygote | 0.0% (0 of 2) |
Vesicular gland | N/A | heterozygote | Not available |
White adipose tissue | N/A | heterozygote | 0.0% (0 of 2) |
An assay measuring the expression of lacZ shows the tissue where the gene is expressed.
Anatomy | Images | Zygosity | Mutant Expr |
---|---|---|---|
Embryo | N/A | heterozygote | 100% (2 of 2) |
Embryo | N/A | homozygote | Ambiguous |
Brain | N/A | heterozygote | 50% (1 of 2) |
Brain | N/A | homozygote | Ambiguous |
Dorsal root ganglion | N/A | heterozygote | 0.0% (0 of 2) |
Dorsal root ganglion | N/A | homozygote | Ambiguous |
Ear | N/A | heterozygote | 0.0% (0 of 2) |
Ear | N/A | homozygote | Ambiguous |
Eye | N/A | heterozygote | 0.0% (0 of 2) |
Eye | N/A | homozygote | Ambiguous |
Footplate | N/A | heterozygote | 0.0% (0 of 2) |
Footplate | N/A | homozygote | Ambiguous |
Forebrain | N/A | heterozygote | 0.0% (0 of 2) |
Forebrain | N/A | homozygote | Ambiguous |
Forelimb | N/A | heterozygote | 0.0% (0 of 2) |
Forelimb | N/A | homozygote | Ambiguous |
Fronto-nasal process | N/A | heterozygote | Ambiguous |
Fronto-nasal process | N/A | homozygote | Ambiguous |
Handplate | N/A | heterozygote | 0.0% (0 of 2) |
Handplate | N/A | homozygote | Ambiguous |
Head | N/A | heterozygote | 100% (2 of 2) |
Head | N/A | homozygote | Ambiguous |
Heart | N/A | heterozygote | 0.0% (0 of 2) |
Heart | N/A | homozygote | Ambiguous |
Hindbrain | N/A | heterozygote | 50% (1 of 2) |
Hindbrain | N/A | homozygote | Ambiguous |
Hindlimb | N/A | heterozygote | 0.0% (0 of 2) |
Hindlimb | N/A | homozygote | Ambiguous |
Liver | N/A | heterozygote | 0.0% (0 of 2) |
Liver | N/A | homozygote | Ambiguous |
Lung | N/A | heterozygote | Ambiguous |
Lung | N/A | homozygote | Ambiguous |
Mandibular process | N/A | heterozygote | 0.0% (0 of 2) |
Mandibular process | N/A | homozygote | Ambiguous |
Maxillary process | N/A | heterozygote | 0.0% (0 of 2) |
Maxillary process | N/A | homozygote | Ambiguous |
Midbrain | N/A | heterozygote | 0.0% (0 of 2) |
Midbrain | N/A | homozygote | Ambiguous |
Nose | N/A | heterozygote | 100% (2 of 2) |
Nose | N/A | homozygote | Ambiguous |
Oral cavity | N/A | heterozygote | 0.0% (0 of 2) |
Oral cavity | N/A | homozygote | Ambiguous |
Skin | N/A | heterozygote | 0.0% (0 of 2) |
Skin | N/A | homozygote | Ambiguous |
Spinal cord | N/A | heterozygote | 50% (1 of 2) |
Spinal cord | N/A | homozygote | Ambiguous |
Tail somite | N/A | heterozygote | 0.0% (0 of 2) |
Tail somite | N/A | homozygote | Ambiguous |
Tail | N/A | heterozygote | 0.0% (0 of 2) |
Tail | N/A | homozygote | Ambiguous |
Background staining occurs in wild type mice and embryos at an incidental rate.
Anatomy | Background staining in controls (WT) |
---|---|
adrenal gland | 0.0% |
aorta | 0.0% |
brain | 0.0% |
brainstem | 0.0% |
brown adipose tissue | 0.0% |
cartilage tissue | 0.0% |
cerebellum | 0.0% |
cerebral cortex | 0.0% |
epididymis | Unavailable |
esophagus | 0.0% |
eye | 0.0% |
heart | 0.0% |
hippocampus | 0.0% |
hypothalamus | 0.0% |
kidney | 0.0% |
large intestine | 0.0% |
liver | 0.0% |
lower urinary tract | 0.0% |
lung | 0.0% |
lymph node | 0.0% |
mammary gland | 0.0% |
midbrain | 0.0% |
olfactory lobe | 0.0% |
ovary | 0.0% |
oviduct | 0.0% |
pancreas | 0.0% |
peripheral nervous system | 0.0% |
peyers patch | 0.0% |
pituitary gland | 0.0% |
prostate gland | 0.0% |
skeletal muscle | 0.0% |
skin | 0.0% |
small intestine | 0.0% |
spinal cord | 0.0% |
spleen | 0.0% |
stomach | 0.0% |
striatum | 0.0% |
submandibular gland | 0.0% |
testis | 0.0% |
thalamus | 0.0% |
thymus | 0.0% |
thyroid gland | 0.0% |
trachea | 0.0% |
urinary bladder | |
uterus | 0.0% |
vascular system | 0.0% |
vesicular gland | Unavailable |
white adipose tissue | 0.0% |
Background staining occurs in wild type mice and embryos at an incidental rate.
Background staining occurs in wild type embryos at a measurable rate.
Anatomy | Background staining in controls(WT) |
---|---|
brain | 0.0% |
dorsal root ganglion | Ambiguous |
ear | 0.0% |
embryo | 0.0% |
eye | 0.0% |
footplate | 0.0% |
forebrain | 0.0% |
forelimb | 0.0% |
fronto-nasal process | Ambiguous |
handplate | 0.0% |
head | 0.0% |
heart | 0.0% |
hindbrain | 0.0% |
hindlimb | 0.0% |
liver | 0.0% |
lung | 0.0% |
mandibular process | 0.0% |
maxillary process | 0.0% |
midbrain | 0.0% |
nose | Ambiguous |
oral cavity | 0.0% |
skin | 0.0% |
spinal cord | Ambiguous |
tail | 0.0% |
tail somite group | 0.0% |
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 associated to Grcc10 by orthology or direct annotation.
Disease | Similarity of phenotypes |
Matching phenotypes | Source |
---|---|---|---|
Temtamy Syndrome | ORPHA:1777 | ||
Temtamy Syndrome | OMIM:218340 |
The table below shows human diseases predicted to be associated to Grcc10 by phenotypic similarity.
Disease | Similarity of phenotypes |
Matching phenotypes | Source |
---|---|---|---|
Venular Insufficiency, Systemic | Cyanosis | OMIM:192700 | |
Sulfhemoglobinemia, Congenital | Cyanosis | OMIM:185460 | |
Diffuse Palmoplantar Keratoderma-Acrocyanosis Syndrome | Acrocyanosis | ORPHA:86918 | |
Methemoglobinemia, Beta Type | Cyanosis | OMIM:617971 | |
Methemoglobinemia, Alpha Type | Cyanosis | OMIM:617973 | |
Cryofibrinogenemia, Familial Primary | Acrocyanosis | OMIM:123540 | |
Breath-Holding Spells | Cyanosis | OMIM:607578 | |
Cyanosis, Transient Neonatal | Jaundice, Cyanosis | OMIM:613977 | |
Cleft Larynx, Posterior | Cyanosis | OMIM:215800 | |
Seizures, Benign Familial Infantile, 3 | Cyanosis | OMIM:607745 | |
Bullous Dystrophy, Hereditary Macular Type | Acrocyanosis | OMIM:302000 | |
Obesity-Hypoventilation Syndrome | Cyanosis | OMIM:257500 | |
Seizures, Benign Familial Infantile, 1 | Cyanosis | OMIM:601764 | |
Perching Syndrome | Cyanosis | OMIM:617055 | |
Peripheral Motor Neuropathy-Dysautonomia Syndrome | Acrocyanosis | ORPHA:2400 | |
Neuralgic Amyotrophy | Acrocyanosis | ORPHA:2901 | |
Laryngeal Abductor Paralysis | Cyanosis | OMIM:150260 | |
Cardiomyopathy-Hypotonia-Lactic Acidosis Syndrome | Cyanosis | ORPHA:91130 | |
Buerger Disease | Acrocyanosis | ORPHA:36258 | |
Phosphoserine Aminotransferase Deficiency | Cyanotic episode | OMIM:610992 | |
Tricuspid Atresia | Cyanosis | ORPHA:1209 | |
Classic Glucose Transporter Type 1 Deficiency Syndrome | Cyanosis | ORPHA:71277 | |
Mitochondrial Phosphate Carrier Deficiency | Cyanosis | OMIM:610773 | |
Benign Familial Infantile Epilepsy | Cyanosis | ORPHA:306 | |
Interstitial Pneumonitis, Desquamative, Familial | Cyanosis | OMIM:263000 | |
Methemoglobinemia Due To Deficiency Of Methemoglobin Reductase | Cyanosis | OMIM:250800 | |
Laryngotracheal Angioma | Cyanosis | ORPHA:137935 | |
Hypoadrenocorticism, Familial | Cyanosis | OMIM:240200 | |
Hereditary Methemoglobinemia | Cyanosis | ORPHA:621 | |
High Altitude Pulmonary Edema | Hypoxemia, Cyanosis | ORPHA:330012 | |
Chronic Pneumonitis Of Infancy | Hypoxemia, Cyanosis | ORPHA:91359 | |
Benign Familial Neonatal Epilepsy | Circumoral cyanosis | ORPHA:1949 | |
Congenital Pulmonary Lymphangiectasia | Cyanosis | ORPHA:2414 | |
Infant Acute Respiratory Distress Syndrome | Hypoxemia, Cyanosis | ORPHA:70587 | |
Acquired Methemoglobinemia | Hypoxemia, Cyanosis | ORPHA:464453 | |
Methemoglobinemia And Ambiguous Genitalia | Cyanosis | OMIM:250790 | |
Laryngotracheoesophageal Cleft | Cyanosis | ORPHA:2004 | |
Ethylmalonic Encephalopathy | Acrocyanosis, Petechiae | ORPHA:51188 | |
Congenital Fibrinogen Deficiency | Cyanosis, Bruising susceptibility, Subcutaneous hemorrhage | ORPHA:335 | |
Cryptogenic Organizing Pneumonia | Hypoxemia, Cyanosis | ORPHA:1302 | |
Restrictive Dermopathy 2 | Cyanosis | OMIM:619793 | |
Congenital Heart Block | Cyanosis | ORPHA:60041 | |
Phosphoserine Aminotransferase Deficiency, Infantile/Juvenile Form | Cyanotic episode | ORPHA:284417 | |
Postsynaptic Congenital Myasthenic Syndromes | Cyanosis | ORPHA:98913 | |
Encephalopathy, Ethylmalonic | Acrocyanosis, Petechiae | OMIM:602473 | |
Pulmonary Alveolar Proteinosis, Acquired | Hypoxemia, Cyanosis | OMIM:610910 | |
Asbestos Intoxication | Hypoxemia, Cyanosis, Oxygen desaturation on exertion | ORPHA:2302 | |
Hsd10 Disease, Infantile Type | Cyanosis | ORPHA:391428 | |
Chiari Malformation Type Ii | Cyanosis | OMIM:207950 | |
Primary Pulmonary Hypoplasia | Hypoxemia, Cyanosis | ORPHA:2257 | |
Combined Oxidative Phosphorylation Defect Type 23 | Cyanosis | ORPHA:444013 | |
Dravet Syndrome | Cyanotic episode | ORPHA:33069 | |
Isolated Right Ventricular Hypoplasia | Hypoxemia, Cyanosis | ORPHA:439 | |
Hyperimmunoglobulinemia D With Periodic Fever | Urticaria, Erythema, Acrocyanosis, Purpura | ORPHA:343 | |
Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Cyanosis | OMIM:261680 | |
Microcephaly, Cerebellar Hypoplasia, And Cardiac Conduction Defect Syndrome | Acrocyanosis | OMIM:614407 | |
Eosinophilic Fasciitis | Acrocyanosis | ORPHA:3165 | |
Acute Interstitial Pneumonia | Hypoxemia, Cyanosis | ORPHA:79126 | |
Choanal Atresia | Cyanosis | ORPHA:137914 | |
Acquired Purpura Fulminans | Acrocyanosis, Macular purpura | ORPHA:49566 | |
Fallot Complex-Intellectual Disability-Growth Delay Syndrome | Cyanosis | ORPHA:3304 | |
Congenitally Uncorrected Transposition Of The Great Arteries | Hypoxemia, Cyanosis | ORPHA:860 | |
Criss-Cross Heart | Cyanosis | ORPHA:1461 | |
Autoimmune Pulmonary Alveolar Proteinosis | Hypoxemia, Cyanosis | ORPHA:747 | |
Waardenburg Syndrome Type 3 | Acrocyanosis | ORPHA:896 | |
Aicardi-Goutieres Syndrome 1 | Erythema, Prolonged neonatal jaundice, Acrocyanosis, Petechiae, Purpura | OMIM:225750 | |
Hereditary Bullous Dystrophy, Macular Type | Acrocyanosis | ORPHA:1867 | |
Sepsis In Premature Infants | Jaundice, Cyanosis, Petechiae, Purpura | ORPHA:90051 | |
Tetrasomy 5P | Cyanosis | ORPHA:3309 | |
Neurodevelopmental Disorder With Impaired Language And Ataxia And With Or Without Seizures | Cyanosis | OMIM:619580 | |
Pulmonary Arteriovenous Malformation | Hypoxemia, Cyanosis, Telangiectasia | ORPHA:2038 | |
Severe Growth Deficiency-Strabismus-Extensive Dermal Melanocytosis-Intellectual Disability Syndrome | Cyanosis | ORPHA:488627 | |
Carnitine-Acylcarnitine Translocase Deficiency | Cyanosis | ORPHA:159 | |
Double Outlet Right Ventricle | Cyanosis | ORPHA:3426 | |
Surfactant Metabolism Dysfunction, Pulmonary, 1 | Cyanosis | OMIM:265120 | |
Congenital Myasthenic Syndrome | Cyanosis | ORPHA:590 | |
Presynaptic Congenital Myasthenic Syndromes | Cyanosis | ORPHA:98914 | |
Pulmonary Capillary Hemangiomatosis | Hypoxemia, Cyanosis | ORPHA:199241 | |
Congenital Tricuspid Valve Dysplasia | Hypoxemia, Cyanosis | ORPHA:555874 | |
Kallmann Syndrome-Heart Disease Syndrome | Cyanosis | ORPHA:2326 | |
Fucosidosis | Acrocyanosis, Vascular skin abnormality | ORPHA:349 | |
Cardiac Valvular Dysplasia 2 | Central cyanosis | OMIM:620067 | |
Surfactant Metabolism Dysfunction, Pulmonary, 2 | Hypoxemia, Cyanosis | OMIM:610913 | |
Eosinophilic Granulomatosis With Polyangiitis | Urticaria, Acrocyanosis, Cutis marmorata, Purpura | ORPHA:183 | |
Surfactant Metabolism Dysfunction, Pulmonary, 3 | Hypoxemia, Cyanosis | OMIM:610921 | |
Meckel Syndrome 14 | Cyanosis | OMIM:619879 | |
Myasthenic Syndrome, Congenital, 21, Presynaptic | Cyanosis | OMIM:617239 | |
Ethylene Glycol Poisoning | Cyanosis | ORPHA:31826 | |
Heterotaxy, Visceral, 7, Autosomal | Cyanosis | OMIM:616749 | |
Structural Heart Defects And Renal Anomalies Syndrome | Cyanosis | OMIM:617478 | |
Complete Atrioventricular Septal Defect | Cyanosis | ORPHA:1329 | |
Telangiectasia, Hereditary Hemorrhagic, Type 4 | Conjunctival telangiectasia, Cyanosis, Lip telangiectasia, Tongue telangiectasia, Nasal mucosa te... | OMIM:610655 | |
Myasthenia Gravis | Acrocyanosis | ORPHA:589 | |
Tarp Syndrome | Cyanosis | ORPHA:2886 | |
Telangiectasia, Hereditary Hemorrhagic, Type 2 | Conjunctival telangiectasia, Cyanosis, Nail bed telangiectasia, Fingerpad telangiectases, Lip tel... | OMIM:600376 | |
Pulmonary Alveolar Microlithiasis | Hypoxemia, Cyanosis, Oxygen desaturation on exertion | ORPHA:60025 | |
Atrial Septal Defect, Ostium Primum Type | Cyanosis | ORPHA:99106 | |
Double Outlet Left Ventricle | Cyanosis | ORPHA:3427 | |
Atrial Septal Defect, Coronary Sinus Type | Cyanosis | ORPHA:99104 | |
Mitochondrial Complex I Deficiency, Nuclear Type 1 | Cyanosis | OMIM:252010 | |
Glycogen Storage Disease Of Heart, Lethal Congenital | Cyanosis | OMIM:261740 | |
Histiocytoid Cardiomyopathy | Cyanosis | ORPHA:137675 | |
Poems Syndrome | Acrocyanosis | ORPHA:2905 | |
Neuropathy, Hereditary Sensory And Autonomic, Type Iii | Acrocyanosis | OMIM:223900 | |
Esophageal Atresia | Cyanosis | ORPHA:1199 | |
Encephalopathy, Acute, Infection-Induced, Susceptibility To, 9 | Cyanosis | OMIM:618426 | |
Telangiectasia, Hereditary Hemorrhagic, Type 1 | Conjunctival telangiectasia, Cyanosis, Telangiectasia of the skin, Nail bed telangiectasia, Finge... | OMIM:187300 | |
Hyperoxaluria, Primary, Type I | Acrocyanosis, Cutis marmorata | OMIM:259900 | |
Familial Dysautonomia | Acrocyanosis | ORPHA:1764 | |
Congenital Tracheomalacia | Cyanosis | ORPHA:95430 | |
Atrial Septal Defect, Ostium Secundum Type | Cyanosis | ORPHA:99103 | |
Unilateral Polymicrogyria | Cyanosis | ORPHA:268943 | |
Absence Of The Pulmonary Artery | Cyanosis, Hypocapnia | ORPHA:980 | |
Abnormal Origin Of Right Or Left Pulmonary Artery From The Aorta | Cyanosis | ORPHA:99050 | |
Heterotaxy, Visceral, 1, X-Linked | Cyanosis | OMIM:306955 | |
Pitt-Hopkins Syndrome | Acrocyanosis | ORPHA:2896 | |
Hutchinson-Gilford Progeria Syndrome | Premature skin wrinkling, Prominent superficial blood vessels, Generalized abnormality of skin, C... | ORPHA:740 | |
Primary Hyperoxaluria | Acrocyanosis, Cutis marmorata | ORPHA:416 | |
Dermatomyositis | Cutaneous photosensitivity, Acrocyanosis, Telangiectasia of the skin, Erythema | ORPHA:221 | |
Postinfectious Vasculitis | Palpable purpura, Acrocyanosis, Cutis marmorata, Vasculitis in the skin | ORPHA:48435 | |
Congenital Tracheal Stenosis | Cyanosis | ORPHA:141127 | |
Rapid-Onset Childhood Obesity-Hypothalamic Dysfunction-Hypoventilation-Autonomic Dysregulation Syndrome | Cyanosis | ORPHA:293987 | |
Aortic Arch Interruption | Cyanosis | ORPHA:2299 | |
Aicardi-Goutières Syndrome | Acrocyanosis, Cutis marmorata, Prolonged neonatal jaundice | ORPHA:51 | |
Cardiac Valvular Dysplasia 1 | Cyanosis | OMIM:212093 | |
Classical Ehlers-Danlos Syndrome | Prematurely aged appearance, Poor wound healing, Ecchymosis, Acrocyanosis, Fragile skin, Bruising... | ORPHA:287 | |
Eisenmenger Syndrome | Hypoxemia, Cyanosis | ORPHA:97214 | |
Truncus Arteriosus | Cyanosis | ORPHA:3384 | |
Congenitally Corrected Transposition Of The Great Arteries | Cyanosis | ORPHA:216694 | |
Coffin-Lowry Syndrome | Acrocyanosis, Cutis marmorata | OMIM:303600 | |
Goodpasture Syndrome | Cyanosis | OMIM:233450 | |
Generalized Arterial Calcification Of Infancy | Cyanosis | ORPHA:51608 | |
Hypermobile Ehlers-Danlos Syndrome | Acrocyanosis | ORPHA:285 | |
Congenital Total Pulmonary Venous Return Anomaly | Cyanosis | ORPHA:99125 | |
Temtamy Syndrome | ORPHA:1777 | ||
Temtamy Syndrome | OMIM:218340 |
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 |
---|---|---|
Grcc10tm1a(EUCOMM)Hmgu | KO first allele (reporter-tagged insertion with conditional potential) | Targeting vectors, ES Cells |
Grcc10tm1(KOMP)Vlcg | Reporter-tagged deletion allele (with selection cassette) | Mice, ES Cells |
Grcc10tm1.1(KOMP)Vlcg | Reporter-tagged deletion allele (post Cre, with no selection cassette) | Mice |
Grcc10tm3(EUCOMM)Wtsi | Reporter-tagged deletion allele (with selection cassette) | Targeting vectors, ES Cells |
Grcc10tm1e(EUCOMM)Hmgu | Targeted, non-conditional allele | ES Cells |
Get highlights of the most important data releases, news and events, delivered straight to your email inbox
Subscribe to newsletter