Gene Gene information from NCBI Gene database.
Entrez ID 256471
Gene name Major facilitator superfamily domain containing 8
Gene symbol MFSD8
Synonyms (NCBI Gene)
CCMDCLN7SLC74A1
Chromosome 4
Chromosome location 4q28.2
Summary This gene encodes a ubiquitous integral membrane protein that contains a transporter domain and a major facilitator superfamily (MFS) domain. Other members of the major facilitator superfamily transport small solutes through chemiosmotic ion gradients. Th
SNPs SNP information provided by dbSNP.
41
SNP ID Visualize variation Clinical significance Consequence
rs118203975 C>T Pathogenic Missense variant, coding sequence variant, non coding transcript variant
rs118203976 C>T Pathogenic Non coding transcript variant, missense variant, coding sequence variant, 3 prime UTR variant
rs118203977 A>C,G Pathogenic Stop gained, coding sequence variant, synonymous variant, non coding transcript variant
rs118203978 T>C,G Pathogenic, uncertain-significance Missense variant, coding sequence variant, non coding transcript variant
rs140948465 G>A,T Likely-pathogenic Missense variant, non coding transcript variant, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
463
miRTarBase ID miRNA Experiments Reference
MIRT044382 hsa-miR-200c-3p CLASH 23622248
MIRT504645 hsa-miR-106a-5p PAR-CLIP 20371350
MIRT504643 hsa-miR-106b-5p PAR-CLIP 20371350
MIRT504642 hsa-miR-17-5p PAR-CLIP 20371350
MIRT504641 hsa-miR-20a-5p PAR-CLIP 20371350
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
56
GO ID Ontology Definition Evidence Reference
GO:0005254 Function Chloride channel activity IBA
GO:0005254 Function Chloride channel activity IDA 34910516
GO:0005254 Function Chloride channel activity IEA
GO:0005739 Component Mitochondrion IEA
GO:0005764 Component Lysosome IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
611124 28486 ENSG00000164073
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8NHS3
Protein name Major facilitator superfamily domain-containing protein 8 (Ceroid-lipofuscinosis neuronal protein 7)
Protein function Outward-rectifying chloride channel involved in endolysosomal chloride homeostasis, membrane fusion and function. Conducts chloride currents up to hundreds of picoamperes. Regulates lysosomal calcium content by reducing the lysosomal membrane po
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07690 MFS_1 42 373 Major Facilitator Superfamily Family
Tissue specificity TISSUE SPECIFICITY: Expressed at very low levels in all tissues tested. {ECO:0000269|PubMed:17564970}.
Sequence
Sequence length 518
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG 
  Lysosome  
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1063
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Cone-rod dystrophy Likely pathogenic; Pathogenic rs559155109 RCV005418155
Hereditary ataxia Likely pathogenic; Pathogenic rs868732642 RCV005626180
Late-infantile neuronal ceroid lipofuscinosis Likely pathogenic; Pathogenic rs571950296, rs2148840216, rs140948465, rs724159970, rs796052742, rs2546165318, rs1057518388, rs200319160, rs587778809, rs749315686, rs1739594685, rs868732642 RCV001831364
RCV005607021
RCV001826401
RCV001276178
RCV005614384
RCV005616496
RCV001833502
RCV000616705
RCV001271142
RCV001271146
RCV001832379
RCV005606764
Macular dystrophy with central cone involvement Likely pathogenic; Pathogenic rs1156864297, rs571950296, rs760049336, rs118203977, rs267607235, rs724159970, rs727502800, rs724159971, rs1578986310, rs2546137643, rs796052752, rs559155109, rs1553950197, rs587778809, rs1578794927
View all (2 more)
RCV001353036
RCV005038169
RCV005023342
RCV005031377
RCV002496222
RCV000149773
RCV000149775
RCV000763521
RCV004771529
RCV002571627
RCV005411364
RCV001542748
RCV005034185
RCV001353040
RCV002497278
RCV002497393
RCV001706719
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Abnormality of the nervous system Conflicting classifications of pathogenicity rs565253666 RCV001814504
Cervical cancer Conflicting classifications of pathogenicity; Likely benign rs75039907, rs796052738 RCV005886632
RCV005892184
Familial cancer of breast Conflicting classifications of pathogenicity rs75039907 RCV005886631
Gastric cancer Benign rs200526922 RCV005870942
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Autism Spectrum Disorder Associate 32722525
Ceroid Lipofuscinosis Neuronal 2 Associate 31721179
Ceroid Lipofuscinosis Neuronal 6 Associate 28586915
Ceroid Lipofuscinosis Neuronal 7 Associate 25333361, 30144815, 30249282, 36833170, 37742391
Epilepsies Myoclonic Associate 22612257
Frontotemporal Dementia Associate 30382371
Frontotemporal Lobar Degeneration Associate 30382371
Glaucoma Open Angle Associate 34348663
Heredodegenerative Disorders Nervous System Associate 28586915
Hypertensive Retinopathy Associate 28586915, 35216386