Gene table of SLC35C1 : solute carrier family 35 member C1

Gene-disease associations table

Disease IDDisease nameSource of annotation with SLC35C1OMIM linkNumber of associated genesgenes
PS212066CONGENITAL DISORDERS OF GLYCOSYLATION, TYPE IIClinVar, OMIM, HUMSAVAR link to OMIM 16B4GALT1, MOGS, SLC35C1, COG4, SLC39A8, TMEM199, COG5, SLC35A2, TMEM165, COG8, COG1, SLC35A1, COG6, MGAT2, CCDC115, COG7

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Annotation of the gene SLC35C1

Associated genes in ENSEMBL
Associated proteins - SwissProt Accession ID
Associated PDB IDs
Cytogenetic Band
Tandem repeats annotation
Transcription regulation as annotated in TRRUST
Associated KEGG pathways
Associated REACTOME pathways
REACTOME pathwayREACTOME IDREACTOME IC
SLC-mediated transmembrane transportR-HSA-4254074.95
Transport of vitamins, nucleosides, and related moleculesR-HSA-4253977.73
Transport of nucleotide sugarsR-HSA-7278029.81
Transmembrane transport of small moleculesR-HSA-3825513.79
Associated GO terms for Molecular function
GO termGO IDGO IC
substrate-specific transmembrane transporter activityGO:00228912.9
nucleobase-containing compound transmembrane transporter activityGO:00159326.34
substrate-specific transporter activityGO:00228922.72
nucleotide-sugar transmembrane transporter activityGO:00053387.54
transporter activityGO:00052152.57
purine nucleotide-sugar transmembrane transporter activityGO:00360809.05
transmembrane transporter activityGO:00228572.82
carbohydrate derivative transporter activityGO:19015056.18
GDP-fucose transmembrane transporter activityGO:00054579.05