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CLN6 (CLN6 transmembrane ER protein)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
54982
Gene nameGene Name - the full gene name approved by the HGNC.
CLN6 transmembrane ER protein
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
CLN6
SynonymsGene synonyms aliases
CLN4A, CLN6A, HsT18960, nclf
ChromosomeChromosome number
15
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
15q23
SummarySummary of gene provided in NCBI Entrez Gene.
This gene is one of eight which have been associated with neuronal ceroid lipofuscinoses (NCL). Also referred to as Batten disease, NCL comprises a class of autosomal recessive, neurodegenerative disorders affecting children. The genes responsible likely
SNPsSNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs3743088 T>C Conflicting-interpretations-of-pathogenicity, uncertain-significance Missense variant, coding sequence variant
rs104894483 C>A,G,T Benign, benign-likely-benign, pathogenic, likely-benign Missense variant, coding sequence variant, stop gained
rs104894484 C>T Pathogenic Missense variant, coding sequence variant
rs104894486 G>A,C Pathogenic Coding sequence variant, synonymous variant, stop gained
rs121908079 ATA>- Pathogenic Coding sequence variant, inframe deletion
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT024862 hsa-miR-215-5p Microarray 19074876
MIRT026355 hsa-miR-192-5p Microarray 19074876
MIRT044786 hsa-miR-320a CLASH 23622248
MIRT043180 hsa-miR-324-5p CLASH 23622248
MIRT040288 hsa-miR-615-3p CLASH 23622248
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001573 Process Ganglioside metabolic process IMP 16857350
GO:0005515 Function Protein binding IPI 17237713, 19235893, 19941651, 30177828, 32296183, 32814053
GO:0005730 Component Nucleolus IDA
GO:0005769 Component Early endosome IDA 17237713
GO:0005783 Component Endoplasmic reticulum IBA 21873635
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID Q9NWW5
Protein name Ceroid-lipofuscinosis neuronal protein 6 (Protein CLN6)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15156 CLN6
30 309
Ceroid-lipofuscinosis neuronal protein 6
Family
Sequence
Sequence length 311
Interactions View interactions
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Action myoclonus-renal failure syndrome Action Myoclonus-Renal Failure Syndrome rs727502772, rs727502773, rs121909118, rs121909119, rs727502781, rs727502782, rs200053119, rs886041078, rs886041077, rs886041076, rs886041075, rs995674389, rs1553948516, rs1578733075 25401298
Dentatorubral pallidoluysian atrophy Dentatorubral-Pallidoluysian Atrophy rs60216939 25401298
Developmental regression Developmental regression rs1224421127
Leukoencephalopathy Leukoencephalopathy rs34757931
Unknown
Disease name Disease term dbSNP ID References
Cerebral atrophy Cerebral atrophy
Dementia Dementia
Developmental dyspraxia Developmental Coordination Disorder 23789114
Disorder of eye Disorder of eye

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