Gene Gene information from NCBI Gene database.
Entrez ID 347734
Gene name Solute carrier family 35 member B2
Gene symbol SLC35B2
Synonyms (NCBI Gene)
HLD26PAPST1SLLUGTrel4
Chromosome 6
Chromosome location 6p21.1
Summary Sulfotransferases (e.g., SULT4A1; MIM 608359) use an activated form of sulfate, 3-prime-phosphoadenosine 5-prime-phosphosulfate (PAPS), as a common sulfate donor for sulfation of glycoproteins, proteoglycans, and glycolipids in the endoplasmic reticulum a
miRNA miRNA information provided by mirtarbase database.
118
miRTarBase ID miRNA Experiments Reference
MIRT027098 hsa-miR-103a-3p Sequencing 20371350
MIRT030466 hsa-miR-24-3p Microarray 19748357
MIRT030466 hsa-miR-24-3p Sequencing 20371350
MIRT031660 hsa-miR-16-5p Sequencing 20371350
MIRT031660 hsa-miR-16-5p Proteomics 18668040
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
27
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane IBA
GO:0000139 Component Golgi membrane IDA 12716889
GO:0000139 Component Golgi membrane IEA
GO:0000139 Component Golgi membrane IEA
GO:0000139 Component Golgi membrane TAS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
610788 16872 ENSG00000157593
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8TB61
Protein name Adenosine 3'-phospho 5'-phosphosulfate transporter 1 (PAPS transporter 1) (Putative MAPK-activating protein PM15) (Putative NF-kappa-B-activating protein 48) (Solute carrier family 35 member B2)
Protein function Probably functions as a 3'-phosphoadenylyl sulfate:adenosine 3',5'-bisphosphate antiporter at the Golgi membranes. Mediates the transport from the cytosol into the lumen of the Golgi of 3'-phosphoadenylyl sulfate/adenosine 3'-phospho 5'-phosphos
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF08449 UAA 111 412 UAA transporter family Family
Tissue specificity TISSUE SPECIFICITY: Highly expressed in the placenta, pancreas, mammary gland and skeletal muscle. Weakly or not expressed in colon, heart and prostate (PubMed:12716889). Expressed in the brain, predominantly in frontal lobe gray matter, subcortical front
Sequence
Sequence length 432
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Transport and synthesis of PAPS
Transport of nucleotide sugars
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
4
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)
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession Evidence Score
Leukodystrophy, hypomyelinating, 26, with chondrodysplasia Pathogenic rs757164153, rs760851221 RCV003152568
RCV003152620
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Primary bone dysplasia with multiple joint dislocations Pathogenic rs760851221 RCV001264615
★★★★☆
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
Hypomyelinating leukodystrophy 11 Conflicting classifications of pathogenicity ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Treacher Collins syndrome 3 Conflicting classifications of pathogenicity ClinVar
★★☆☆☆
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
B-Cell Lymphomas B-Cell Lymphoma BEFREE 20809502
★☆☆☆☆
Found in Text Mining only
Breast Carcinoma Breast Carcinoma BEFREE 25124574
★☆☆☆☆
Found in Text Mining only
Breast Neoplasms Breast neoplasm Pubtator 25124574 Associate
★☆☆☆☆
Found in Text Mining only
Carcinoma Ductal Breast Ductal carcinoma of breast Pubtator 25124574 Associate
★☆☆☆☆
Found in Text Mining only
Cardiomyopathy, Familial Idiopathic Cardiomyopathy BEFREE 25124574
★☆☆☆☆
Found in Text Mining only
Chronic Lymphocytic Leukemia Lymphocytic Leukemia BEFREE 11342346, 12454822, 1376056, 16109617, 25700432, 8946198, 9888704
★☆☆☆☆
Found in Text Mining only
Colorectal Neoplasms Colorectal neoplasm Pubtator 27756247 Associate
★☆☆☆☆
Found in Text Mining only
Hereditary Multiple Exostoses Multiple congenital exostosis BEFREE 21506131
★☆☆☆☆
Found in Text Mining only
Invasive Ductal Breast Carcinoma Invasive Duct and Lobular Carcinoma BEFREE 25124574
★☆☆☆☆
Found in Text Mining only
Lymphoma Lymphoma BEFREE 31187468
★☆☆☆☆
Found in Text Mining only