SLC35G2 (solute carrier family 35 member G2)

Gene Gene information from NCBI Gene database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID 80723
Gene name Solute carrier family 35 member G2
Gene symbol SLC35G2
Synonyms (NCBI Gene)
TMEM22
Chromosome 3
Chromosome location 3q22.3
miRNA miRNA information provided by mirtarbase database.
44
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all (44)
miRTarBase ID miRNA Experiments Reference
MIRT550120 hsa-miR-3662 PAR-CLIP 21572407
MIRT305134 hsa-miR-3617-5p PAR-CLIP 21572407
MIRT305132 hsa-miR-641 PAR-CLIP 21572407
MIRT090510 hsa-miR-5197-5p PAR-CLIP 21572407
MIRT305128 hsa-miR-181a-5p PAR-CLIP 21572407
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
11
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all (11)
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 28514442, 32296183, 33961781
GO:0005794 Component Golgi apparatus IDA
GO:0005886 Component Plasma membrane IBA
GO:0005886 Component Plasma membrane IDA 19148500
GO:0005886 Component Plasma membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
617812 28480 ENSG00000168917
Protein Protein information from UniProt database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8TBE7
Protein name Solute carrier family 35 member G2 (Transmembrane protein 22)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00892 EamA 102 → 238 EamA-like transporter family Family
PF00892 EamA 255 → 390 EamA-like transporter family Family
Sequence
Sequence length 412
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
Gene miRNA Gene ontology Other IDs Protein Associated diseases
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)
Show/Hide Unknown Diseases (2)
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
Melanoma Uncertain significance ClinVar
CTD
★★★★★
★★★☆☆
Reported in Unknown/Other Associations (≥2 sources)
MITOCHONDRIAL COMPLEX I DEFICIENCY — Disgenet, GenCC
Disgenet, GenCC
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Show/Hide Text Mining Associations (2)
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Carcinoma Hepatocellular Associate 35637633, 40055377
★★★★★
★☆☆☆☆
Found in Text Mining only
Chemical and Drug Induced Liver Injury Associate 35637633
★★★★★
★☆☆☆☆
Found in Text Mining only