Gene Gene information from NCBI Gene database.
Entrez ID 23302
Gene name WSC domain containing 1
Gene symbol WSCD1
Synonyms (NCBI Gene)
-
Chromosome 17
Chromosome location 17p13.2
miRNA miRNA information provided by mirtarbase database.
118
miRTarBase ID miRNA Experiments Reference
MIRT486051 hsa-miR-4781-5p PAR-CLIP 20371350
MIRT486050 hsa-miR-3960 PAR-CLIP 20371350
MIRT486049 hsa-miR-8072 PAR-CLIP 20371350
MIRT486048 hsa-miR-4467 PAR-CLIP 20371350
MIRT486047 hsa-miR-3180 PAR-CLIP 20371350
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
6
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane IEA
GO:0000139 Component Golgi membrane ISS
GO:0005794 Component Golgi apparatus IEA
GO:0008146 Function Sulfotransferase activity IEA
GO:0008146 Function Sulfotransferase activity ISS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
619584 29060 ENSG00000179314
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q658N2
Protein name Sialate:O-sulfotransferase 1 (WSC domain-containing protein 1)
Protein function Sialate:O-sulfotransferase which catalyzes 8-O-sulfation at the Sia-glycan level using 3'-phosphoadenosine 5'-phosphosulfate (PAPS) as a donor, forming 8-O-sulfated Sia (Sia8S)-glycans. Displays selectivity toward glycolipids such as GM1 ganglio
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01822 WSC 145 224 WSC domain Domain
PF01822 WSC 248 330 WSC domain Domain
PF00685 Sulfotransfer_1 416 525 Sulfotransferase domain Domain
Sequence
MAKPFFRLQKFLRRTQFLLFFLTAAYLMTGSLLLLQRVRVALPQGPRAPGPLQTLPVAAV
ALGVGLLDSRALHDPRVSPELLLGVDMLQSPLTRPRPGPRWLRSRNSELRQLRRRWFHHF
MSDSQGPPALGPEAARPAIHSRGTYIGCFSDDGHERTLKGAVFYDLRKMTVSHCQDACAE
RSYVYAGLEAGAECYCGNRLPAVSVGLEECNHECKGEKGSVCGA
VDRLSVYRVDELQPGS
RKRRTATYRGCFRLPENITHAFPSSLIQANVTVGTCSGFCSQKEFPLAILRGWECYCAYP
TPRFNLRDAMDSSVCGQDPEAQRLAEYCEV
YQTPVQDTRCTDRRFLPNKSKVFVALSSFP
GAGNTWARHLIEHATGFYTGSYYFDGTLYNKGFKGEKDHWRSRRTICVKTHESGRREIEM
FDSAILLIRNPYRSLVAEFNRKCAGHLGYAADRNWKSKEWPDFVNSYASWWSSHVLDWLK
YGKRLLVVHYEELRRSLVPTLREMVAFLNVSVSEERLLCVENNKE
GSFRRRGRRSHDPEP
FTPEMKDLINGYIRTVDQALRDHNWTGLPREYVPR
Sequence length 575
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
13
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
BIPOLAR DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CORNEAL NEOVASCULARIZATION GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ESSENTIAL TREMOR GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
HYPOTENSION GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Liver neoplasms Liver neoplasms CTD_human_DG 19233941
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Malignant neoplasm of liver Liver Cancer CTD_human_DG 19233941
★☆☆☆☆
Found in Text Mining only