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Search results for "Tmem42" in category
Genes/Alleles
(2 EMMA strains found)
EMMA ID
Strain name
Gene/Transgene symbol
Disease count
EM:14196
C57BL/6N-Tmem42
tm1b(KOMP)Wtsi
/WtsiPh
Tmem42
Register interest
EM:08045
C57BL/6N-A
tm1Brd
Tmem42
tm1a(KOMP)Wtsi
/WtsiBiat
Tmem42
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Cardiovascular system
Heart disease
Atrioventricular spetal defect
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Jervell-Lange Nielsen syndrome
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Endocrine system
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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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Autosomal recessive early-onset Parkinson disease 7
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Peripheral nervous system disease
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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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Mental health
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Inherited metabolic disorder
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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
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Chondrodysplasia punctata
X-linked chondrodysplasia punctata
Monogenic disease
Branchiootorenal syndrome
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Denys-Drash syndrome
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Curated Disease Models
