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Search results for "Tmem132a" in category
Genes/Alleles
(1 EMMA strains found)
EMMA ID
Strain name
Gene symbol
Disease count
EM:09726
C57BL/6NTac-Tmem132a
tm1a(KOMP)Wtsi
/WtsiH
Tmem132a
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Browse curated disease models
Cardiovascular system
Heart disease
Atrioventricular spetal defect
Dilated cardiomyopathy
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Jervell-Lange Nielsen syndrome
Tetralogy of Fallot
Endocrine system
Parathyroid gland disease
Primary hyperaldosteronism
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Inflammatory bowel disease disease
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Immune system
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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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Epidermolysis bullosa simplex Dowling-Meara type
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Musculoskeletal system
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Rigid spine muscular dystrophy 1
Muscle tissue
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Ehlers-Danlos syndrome
systemic scleroderma
Bone disease
Autosomal recessive osteopetrosis 2
Clubfoot
Craniosynostosis
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Muenke Syndrome
Osteogenesis imperfecta type
Osteogenesis imperfecta type 2
Osteogenesis imperfecta type 3
Rheumatoid arthritis
Saethre-Chotzen syndrome
Spondyloepiphyseal dysplasia congenita
X-linked hypophosphatemic rickets
Nervous system
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Alzheimer's disease
Amyotrophic lateral sclerosis type 1
Autosomal recessive early-onset Parkinson disease 7
Multiple sclerosis
Parkinson disease
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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Nevoid basal cell carcinoma syndrome
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Benign neoplasm
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Mental health
Developmental disorder of mental health
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Metabolism
Acquired metabolic disease
Familial hypocalciuric hypercalcemia 1
Metabolic syndrome X
Obesity
Diabetes mellitus
Transient neonatal diabetes mellitus
Type 1 diabetes mellitus
Inherited metabolic disorder
Alkaptonuria
Aspartylglucosaminuria
Cutaneous porphyria
Glycogen storage disease III
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
Cardiofaciocutaneous syndrome
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CHARGE syndrome
CHARGE syndrome
Sudden infant death syndrome
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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
