Gene Gene information from NCBI Gene database.
Entrez ID 728661
Gene name Solute carrier family 35 member E2B
Gene symbol SLC35E2B
Synonyms (NCBI Gene)
SLC35E2
Chromosome 1
Chromosome location 1p36.33
miRNA miRNA information provided by mirtarbase database.
1255
miRTarBase ID miRNA Experiments Reference
MIRT050794 hsa-miR-17-5p CLASH 23622248
MIRT709647 hsa-miR-181d-3p HITS-CLIP 19536157
MIRT709646 hsa-miR-3622b-5p HITS-CLIP 19536157
MIRT709645 hsa-miR-6716-5p HITS-CLIP 19536157
MIRT709644 hsa-miR-4253 HITS-CLIP 19536157
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:0001835 Process Blastocyst hatching IEA
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
619315 33941 ENSG00000189339
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P0CK96
Protein name Solute carrier family 35 member E2B
Protein function Putative transporter.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03151 TPT 73 368 Triose-phosphate Transporter family Family
Sequence
Sequence length 405
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
High myopia Uncertain significance ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SEVERE MYOPIA Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations