Gene Gene information from NCBI Gene database.
Entrez ID 339665
Gene name Solute carrier family 35 member E4
Gene symbol SLC35E4
Synonyms (NCBI Gene)
-
Chromosome 22
Chromosome location 22q12.2
miRNA miRNA information provided by mirtarbase database.
167
miRTarBase ID miRNA Experiments Reference
MIRT646861 hsa-miR-6819-3p HITS-CLIP 23824327
MIRT646860 hsa-miR-6877-3p HITS-CLIP 23824327
MIRT646859 hsa-miR-5088-5p HITS-CLIP 23824327
MIRT646858 hsa-miR-1245a HITS-CLIP 23824327
MIRT646856 hsa-miR-8079 HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
5
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0005794 Component Golgi apparatus IBA
GO:0015297 Function Antiporter activity IBA
GO:0016020 Component Membrane IEA
GO:0055085 Process Transmembrane transport IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6ICL7
Protein name Solute carrier family 35 member E4
Protein function Putative transporter.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03151 TPT 47 326 Triose-phosphate Transporter family Family
Sequence
Sequence length 350
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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
ATRIAL FIBRILLATION GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations