Protein CLN8 is a protein that in humans is encoded by the CLN8 gene. This gene encodes a transmembrane protein that localizes to the endoplasmic reticulum...
9 KB (894 words) - 05:35, 29 August 2023
to the Golgi apparatus upon recruitment by a complex composed of CLN6 and CLN8 proteins. The enzymes are transported from the Golgi apparatus to lysosomes...
43 KB (4,709 words) - 17:51, 12 June 2024
mutations in the CLN8 gene. The disease is now known as the mildest form of NCL. There are two forms of this mutated gene: 1-CLN8 and 2-CLN8. 1-CLN8 is known...
9 KB (1,065 words) - 01:40, 22 February 2024
Type 7 CLN7 610951 MFSD8 Type 8 CLN8 Northern epilepsy, progressive epilepsy with mental retardation (EPMR) 610003 CLN8 Type 8 Turkish late infantile (Turkish...
39 KB (4,424 words) - 07:07, 22 June 2024
functions as a lysosomal transmembrane protein. Northern epilepsy: CLN8 encodes for CLN8, a transmembrane protein of the endoplasmic reticulum. Late infantile...
31 KB (3,426 words) - 04:30, 2 July 2024
variant (CLN6) Type 7 CLN7 Type 8 Northern epilepsy (CLN8) Type 8 Turkish late infantile (CLN8) Type 9 German/Serbian late infantile (unknown) Type 10...
18 KB (1,819 words) - 05:23, 3 April 2024
code Genes related to neuronal ceroid lipofuscinosis: CLN3, CLN5, CLN6, CLN8 This disambiguation page lists articles associated with the title CLN. If...
877 bytes (129 words) - 01:45, 14 January 2024
lipofuscinosis are found in the Finnish heritage: CLN1, CLN3, CLN5, and CLN8. Names for conditions associated with these subtypes include infantile neuronal...
13 KB (1,459 words) - 20:06, 6 May 2024
HGNC:2074 Q13286 3201 CLN5 HGNC:2076 O75503 3202 CLN6 HGNC:2077 Q9NWW5 3203 CLN8 HGNC:2079 Q9UBY8 3204 CLNK HGNC:17438 Q7Z7G1 3205 CLNS1A HGNC:2080 P54105...
277 KB (17 words) - 23:17, 27 April 2024
accessibility complex 1 CHRNA2: cholinergic receptor, nicotinic, alpha 2 (neuronal) CLN8: ceroid-lipofuscinosis, neuronal 8 CNGB3: cyclic nucleotide gated channel...
29 KB (1,896 words) - 23:26, 28 March 2024