Gene Gene information from NCBI Gene database.
Entrez ID 79939
Gene name Solute carrier family 35 member E1
Gene symbol SLC35E1
Synonyms (NCBI Gene)
-
Chromosome 19
Chromosome location 19p13.11
miRNA miRNA information provided by mirtarbase database.
1249
miRTarBase ID miRNA Experiments Reference
MIRT699356 hsa-miR-1295b-5p HITS-CLIP 23313552
MIRT699355 hsa-miR-1912 HITS-CLIP 23313552
MIRT699354 hsa-miR-3130-5p HITS-CLIP 23313552
MIRT699353 hsa-miR-4482-5p HITS-CLIP 23313552
MIRT699352 hsa-miR-6741-3p HITS-CLIP 23313552
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:0005515 Function Protein binding IPI 32296183
GO:0005794 Component Golgi apparatus IBA
GO:0005794 Component Golgi apparatus IDA
GO:0015297 Function Antiporter activity IBA
GO:0016020 Component Membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
620337 20803 ENSG00000127526
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96K37
Protein name Solute carrier family 35 member E1
Protein function Putative transporter.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03151 TPT 28 333 Triose-phosphate Transporter family Family
Sequence
Sequence length 410
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Thyroid cancer, nonmedullary, 1 Uncertain significance 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
Thyroid Cancer Papillary Papillary thyroid cancer Pubtator 34590520 Associate
★☆☆☆☆
Found in Text Mining only