Gene Details | GeDiPNet - Complete Gene Info, Disease Associations & Pathways

Gene Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.	80723
Gene name Gene Name - the full gene name approved by the HGNC.	Solute carrier family 35 member G2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.	SLC35G2
Synonyms (NCBI Gene) Gene synonyms aliases	TMEM22
Chromosome Chromosome number	3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.	3q22.3

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
MIRT305129	hsa-miR-181b-5p	PAR-CLIP	21572407
MIRT305130	hsa-miR-181c-5p	PAR-CLIP	21572407
MIRT305131	hsa-miR-181d-5p	PAR-CLIP	21572407
MIRT305133	hsa-miR-4262	PAR-CLIP	21572407
MIRT550119	hsa-miR-4724-5p	PAR-CLIP	21572407
MIRT550118	hsa-miR-34a-5p	PAR-CLIP	21572407
MIRT550117	hsa-miR-34c-5p	PAR-CLIP	21572407
MIRT550116	hsa-miR-449a	PAR-CLIP	21572407
MIRT550115	hsa-miR-449b-5p	PAR-CLIP	21572407
MIRT550114	hsa-miR-548au-3p	PAR-CLIP	21572407
MIRT090501	hsa-miR-30a-5p	PAR-CLIP	21572407
MIRT090505	hsa-miR-30b-5p	PAR-CLIP	21572407
MIRT090503	hsa-miR-30c-5p	PAR-CLIP	21572407
MIRT090504	hsa-miR-30d-5p	PAR-CLIP	21572407
MIRT090506	hsa-miR-30e-5p	PAR-CLIP	21572407
MIRT550113	hsa-miR-376a-3p	PAR-CLIP	21572407
MIRT550112	hsa-miR-376b-3p	PAR-CLIP	21572407
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
MIRT305129	hsa-miR-181b-5p	PAR-CLIP	21572407
MIRT305130	hsa-miR-181c-5p	PAR-CLIP	21572407
MIRT305131	hsa-miR-181d-5p	PAR-CLIP	21572407
MIRT305133	hsa-miR-4262	PAR-CLIP	21572407
MIRT550119	hsa-miR-4724-5p	PAR-CLIP	21572407
MIRT550118	hsa-miR-34a-5p	PAR-CLIP	21572407
MIRT550117	hsa-miR-34c-5p	PAR-CLIP	21572407
MIRT550116	hsa-miR-449a	PAR-CLIP	21572407
MIRT550115	hsa-miR-449b-5p	PAR-CLIP	21572407
MIRT550114	hsa-miR-548au-3p	PAR-CLIP	21572407
MIRT090501	hsa-miR-30a-5p	PAR-CLIP	21572407
MIRT090505	hsa-miR-30b-5p	PAR-CLIP	21572407
MIRT090503	hsa-miR-30c-5p	PAR-CLIP	21572407
MIRT090504	hsa-miR-30d-5p	PAR-CLIP	21572407
MIRT090506	hsa-miR-30e-5p	PAR-CLIP	21572407
MIRT550113	hsa-miR-376a-3p	PAR-CLIP	21572407
MIRT550112	hsa-miR-376b-3p	PAR-CLIP	21572407

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
GO:0005886	Component	Plasma membrane	TAS	19148500
GO:0016020	Component	Membrane	IEA
GO:0030672	Component	Synaptic vesicle membrane	IDA	34269178
GO:0030672	Component	Synaptic vesicle membrane	IEA
GO:0031410	Component	Cytoplasmic vesicle	IEA
GO:0045202	Component	Synapse	IEA

MIM	HGNC	e!Ensembl
617812	28480	ENSG00000168917

Protein

UniProt ID

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

MDTSPSRKYPVKKRVKIHPNTVMVKYTSHYPQPGDDGYEEINEGYGNFMEENPKKGLLSE
MKKKGRAFFGTMDTLPPPTEDPMINEIGQFQSFAEKNIFQSRKMWIVLFGSALAHGCVAL
ITRLVSDRSKVPSLELIFIRSVFQVLSVLVVCYYQEAPFGPSGYRLRLFFYGVCNVISIT
CAYTSFSIVPPSNGTTMWRATTTVFSAILAFLLVDEKMAYVDMATVVCSILGVCLVMIPN
IVDEDNSLLNAWKEAFGYTMTVMAGLTTALSMIVYRSIKEKISMWTALFTFGWTGTIWGI
STMFILQEPIIPLDGETWSYLIAICVCSTAAFLGVYYALDKFHPALVSTVQHLEIVVAMV
LQLLVLHIFPSIYDVFGGVIIMISVFVLAGYKLYWRNLRKQDYQEILDSPIK

Sequence length

412

Interactions

View interactions

Show/Hide Unknown Diseases (1)

Disease merge term	Disease name	Evidence	References	Source
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Mitochondrial Complex Deficiency	mitochondrial complex I deficiency	N/A	N/A	GenCC

Show/Hide Text Mining Associations (2)

Disease Name	Relationship Type	References
Associations from Text Mining Disease associations identified through Pubtator
Carcinoma Hepatocellular	Associate	35637633, 40055377
Chemical and Drug Induced Liver Injury	Associate	35637633

SLC35G2 (solute carrier family 35 member G2)