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The welfare and ethical treatment of animal models in research is very important for INFRAFRONTIER.
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EMMA Overview
Everything you need to know about the European Mouse Mutant Archive – EMMA.
Cryopreservation
EMMA archives your mouse/rat mutant free of charge.
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EMMA repository conditions, MTAs, policy on licensing and use restriction.
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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
INFRAFRONTIER offers a host of state-of-the-art services to the biomedical community with the aim to understand and combat human diseases.
Rodent Model Generation
Generation of rodent models using latest genome-editing technologies.
Strain Distribution
Distribution of mutant mouse/rat lines around the globe as frozen gametes or live cohorts.
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Archiving of mutant mouse/rat models generated by researchers around the world.
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Mouse model phenotyping platforms incorporating whole-system screens.
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Germ-free derivation of mouse strains for gnotobiotic studies.
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CD11
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IMPC
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Search results for "Ltbp1" in category
Genes/Alleles
(2 EMMA strains found)
EMMA ID
Strain name
Gene/Transgene symbol
Disease count
EM:02446
B6.129X1-Ltbp1
tm1Rawe
/Cnrm
Ltbp1
1
Order (in stock)
EM:05861
B6Brd;B6N-Tyr
c-Brd
Ltbp1
tm1a(EUCOMM)Wtsi
/WtsiH
Ltbp1
1
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
Hyperparathyroidism
Gastrointestinal system
Intestinal disease
Hirschsprung disease
Inflammatory bowel disease disease
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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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Rigid spine muscular dystrophy 1
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systemic scleroderma
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Autosomal recessive osteopetrosis 2
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Osteogenesis imperfecta type
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Nervous system
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Alzheimer's disease
Amyotrophic lateral sclerosis type 1
Autosomal recessive early-onset Parkinson disease 7
Multiple sclerosis
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Peripheral nervous system disease
Charcot-Marie-Tooth disease type 1A
Charcot-Marie-Tooth disease type 2A2
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
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Urinary system
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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
Obesity
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Transient neonatal diabetes mellitus
Type 1 diabetes mellitus
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
Wiskott-Aldrich syndrome
Waardenburg syndrome type 1
Waardenburg syndrome type 2A
Xeroderma pigmentosum variant type
Syndrome
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CHARGE syndrome
CHARGE syndrome
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Sudden infant death syndrome
Selected strain collections
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TET-expression systems
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
