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EMMA Overview
Everything you need to know about the European Mouse Mutant Archive – EMMA.
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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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CD11
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Search results for "Ndufa10" in category
Genes/Alleles
(2 EMMA strains found)
EMMA ID
Strain name
Gene symbol
Disease count
EM:08723
C57BL/6NTac-Ndufa10
tm1e(EUCOMM)Hmgu
/Ieg
Ndufa10
1
Order (in stock)
EM:10048
C57BL/6N-Ndufa10
tm1e.1(EUCOMM)Hmgu
/Ieg
Ndufa10
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
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Gastrointestinal system
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Immune system
Hypersensitivity reaction disease
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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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systemic scleroderma
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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
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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
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Retinitis pigmentosa 40
Persistent hyperplastic primary vitreous
Respiratory system
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Urinary system
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Mental health
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Metabolism
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Alkaptonuria
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Neuronal ceroid lipofuscinosis 3
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Neuronal ceroid lipofuscinosis 10
Favism
Genetic disease
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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 2A
Xeroderma pigmentosum variant type
Syndrome
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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
