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EMMA Overview
Everything you need to know about the European Mouse Mutant Archive – EMMA.
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EMMA archives your mouse/rat mutant free of charge.
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Access to over 8700 mouse mutants and a couple of tens of rat mutants.
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Strains originated by large-scale projects archived and distributed by EMMA.
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Services Overview
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Generation of rodent models using latest genome-editing technologies.
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Distribution of mutant mouse/rat lines around the globe as frozen gametes or live cohorts.
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Search results for "Ptpn22" in category
Genes/Alleles
(2 EMMA strains found)
EMMA ID
Strain name
Gene/Transgene symbol
Disease count
EM:06015
C57BL/6NTac-Ptpn22
tm1e(EUCOMM)Wtsi
/Cnrm
Ptpn22
Order (in stock)
EM:06017
C57BL/6NTac-Ptpn22
tm1e(EUCOMM)Wtsi
/Cnrm
Ptpn22
Order (in stock)
Browse curated disease models
Cardiovascular system
Heart disease
Atrioventricular spetal defect
Dilated cardiomyopathy
Hypertrophic cardiomyopathy
Jervell-Lange Nielsen syndrome
Tetralogy of Fallot
Endocrine system
Parathyroid gland disease
Primary hyperaldosteronism
Adrenal gland disease
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Gastrointestinal system
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Hirschsprung disease
Inflammatory bowel disease disease
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Primary billiary cirrhosis
Immune system
Hypersensitivity reaction disease
Autoimmune lymphoproliferative syndrome
Sjogren's syndrome
Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome
Lymphatic system disease
Familial hemophagocytic lymphohistiocytosis 2
Hereditary lymphedema
Primary immunodeficiency disease
DNA ligase IV deficiency
T-cell immunodeficiency, congenital alopecia, and nail dystrophy
Hematopoietic system
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Leukocyte disease
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Integumentary system
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Musculoskeletal system
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Rigid spine muscular dystrophy 1
Muscle tissue
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systemic scleroderma
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Autosomal recessive osteopetrosis 2
Clubfoot
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Muenke Syndrome
Osteogenesis imperfecta type
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Osteogenesis imperfecta type 3
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Spondyloepiphyseal dysplasia congenita
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Nervous system
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Autosomal recessive early-onset Parkinson disease 7
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Peripheral nervous system disease
Charcot-Marie-Tooth disease type 1A
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Charcot-Marie-Tooth disease type 2D
Charcot-Marie-Tooth disease X-linked dominant 1
Brain disease
Basal ganglia calcification
Creutzfeldt-Jakob disease
Early infantile epileptic encephalopathy
Sensory system disease
Aniridia
Autosomal dominant nonsyndromic deafness 12
Autosomal dominant nonsyndromic deafness 36
Autosomal recessive nonsyndromic deafness 1A
Autosomal recessive nonsyndromic deafness 4A
Autosomal recessive nonsyndromic deafness 31
Autosomal recessive nonsyndromic deafness 7
Autosomal recessive nonsyndromic deafness 42
Cataract
Cataract 1 multiple types
Cataract 19 multiple types
Cataract 20 multiple types
Cataract 21 multiple types
Congenital stationary night blindness
Otitis media
Ocular albinism
Retinitis pigmentosa 40
Persistent hyperplastic primary vitreous
Respiratory system
Lung disease
Pulmonary alveolar proteinosis
Urinary system
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Cellular proliferation
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Benign neoplasm
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Mental health
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Metabolism
Acquired metabolic disease
Familial hypocalciuric hypercalcemia 1
Metabolic syndrome X
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Inherited metabolic disorder
Alkaptonuria
Aspartylglucosaminuria
Cutaneous porphyria
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Neuronal ceroid lipofuscinosis 3
Neuronal ceroid lipofuscinosis 7
Neuronal ceroid lipofuscinosis 10
Favism
Genetic disease
Ciliopathy
Joubert syndrome 6
Meckel syndrome
Primary ciliary dyskinesia 7
Maturity-onset diabetes of the young
Maturity-onset diabetes of the young
Maturity-onset diabetes of the young type 2
Chondrodysplasia punctata
X-linked chondrodysplasia punctata
Monogenic disease
Branchiootorenal syndrome
Clouston syndrome<
Denys-Drash syndrome
Microphthalmia with limb anomalies
Nephronophthisis 2
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Waardenburg syndrome type 1
Waardenburg syndrome type 2A
Xeroderma pigmentosum variant type
Syndrome
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CHARGE syndrome
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Sudden infant death syndrome
Selected strain collections
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Genome Editing Mice for Medicine – GEMM
Wellcome Trust Knockout Mouse Resource
PHENOMIN-ICS NR Collection
PHENOMIN-ICS Recombinase collection
Mosaic Analysis with Double Markers (MADM)
Rat strains
Curated Disease Models
