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Gene |
Common name for disease |
Proposed New Nomenclature |
Gene Product (protein) |
Protein description |
Online
Mendelian Inheritance in Man¨ |
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CLN1 |
Infantile classic |
CLN1 disease,
infantile |
Palmitoyl protein
thioesterase 1, PPT1 |
soluble lysosomal
enzyme deficiency |
256730 |
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CLN1
disease, late infantile |
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CLN1
disease, juvenile |
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CLN1
disease, adult |
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CLN2 |
Late infantile
classic |
CLN2 disease,
late infantile |
Tripeptidyl peptidase
1, TPP1 |
soluble lysosomal
enzyme deficiency |
204500 |
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CLN2
disease, juvenile |
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CLN3 |
Juvenile
classic |
CLN3 disease |
CLN3
transmembrane protein |
transmembrane
protein |
204200 |
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CLN4/DNAJC5 |
Adult autosomal
dominant Batten, Kuf's disease, Ceroid Lipofuscinosis, Parry type |
CLN4 disease |
Cysteine
string proteinα |
secretory vesicle protein |
162350 |
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CLN5 |
Finnish variant Late
infantile |
CLN5 disease,
late infantile |
Ceroid-lipofuscinosis
neuronal protein 5 |
soluble lysosomal
(non)enzyme deficiency |
256731 |
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CLN5
disease, juvenile |
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CLN5
disease, adult |
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CLN6 |
Early juvenile
variant or late infantile variant |
CLN6 disease,
late infantile |
Ceroid-lipofuscinosis
neuronal protein 6 |
transmembrane
protein, endoplasmic reticulum |
601780 |
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CLN6
disease, juvenile |
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|
CLN6 |
Adult
CLN6 disease |
CLN6
disease, adult |
Ceroid-lipofuscinosis neuronal
protein 6 |
transmembrane protein,
endoplasmic reticulum |
204300 |
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CLN7 |
Late infantile
variant |
CLN7 disease,
late infantile |
Major facilitator superfamily
domain-containing protein 8 |
transmembrane protein,
endolysosomal transporter |
610951 |
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CLN8 |
Late infantile
variant, EPMR (progressive epilepsy with mental retardation) |
CLN8 disease,
late infantile |
unknown transmembrane protein,
ER, ER-Golgi intermediate complex |
transmembrane protein,
endoplasmic reticulum , ER-Golgi intermediate complex |
600143 |
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CLN10/CTSD |
Congenital classic,
late infantile, adult |
CLN10 disease,
congenital |
Cathepsin D |
soluble lysosomal
enzyme deficiency |
610127 |
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CLN10
disease, late infantile |
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CLN10
disease, juvenile |
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CLN10
disease, adult |
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CLN11/GRN |
Adult
(heterozygous mutations cause frontotemporal lobar dementia) |
CLN11 disease,
adult |
Progranulin |
non enzyme;
function of protein poorly understood |
To Be
Determined (TBD) |
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CLN12/ATP13A2 |
CLN12 disease,
juvenile (mutations also cause Kufor-Rakeb syndrome) |
CLN12 disease,
juvenile |
P-type ATPase |
non enzyme;
function of protein poorly understood |
TBD |
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CLN13 |
Adult Kufs type
B |
CLN13 disease,
adult |
Cathepsin F |
soluble
lysosomal enzyme deficiency |
TBD |
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CLN14/KCTD7 |
CLN14 disease,
infantile |
CLN14 disease,
infantile |
Potassium
channel tetramerization domain-containing protein 7 |
probable
transmembrane protein voltage-gated potassium channel complex |
TBD |
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(Williams
and Mole 2012, Cooper, Mole, Williams 2012) |
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