Gene Gene information from NCBI Gene database.
Entrez ID 140679
Gene name Solute carrier family 32 member 1
Gene symbol SLC32A1
Synonyms (NCBI Gene)
DEE114GEFSP12VGATVIAATVIAAT GEFSP12
Chromosome 20
Chromosome location 20q11.23
Summary The protein encoded by this gene is an integral membrane protein involved in gamma-aminobutyric acid (GABA) and glycine uptake into synaptic vesicles. The encoded protein is a member of amino acid/polyamine transporter family II. [provided by RefSeq, Jul
miRNA miRNA information provided by mirtarbase database.
26
miRTarBase ID miRNA Experiments Reference
MIRT019437 hsa-miR-148b-3p Microarray 17612493
MIRT1359901 hsa-miR-138 CLIP-seq
MIRT1359902 hsa-miR-1587 CLIP-seq
MIRT1359903 hsa-miR-1908 CLIP-seq
MIRT1359904 hsa-miR-3180 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
58
GO ID Ontology Definition Evidence Reference
GO:0001762 Process Beta-alanine transport IEA
GO:0001762 Process Beta-alanine transport ISS
GO:0003333 Process Amino acid transmembrane transport IEA
GO:0005886 Component Plasma membrane TAS
GO:0006811 Process Monoatomic ion transport TAS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
616440 11018 ENSG00000101438
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9H598
Protein name Vesicular inhibitory amino acid transporter (GABA and glycine transporter) (Solute carrier family 32 member 1) (Vesicular GABA transporter) (hVIAAT)
Protein function Antiporter that exchanges vesicular protons for cytosolic 4-aminobutanoate or to a lesser extend glycine, thus allowing their secretion from nerve terminals. The transport is equally dependent on the chemical and electrical components of the pro
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01490 Aa_trans 114 513 Transmembrane amino acid transporter protein Family
Tissue specificity TISSUE SPECIFICITY: Retina. Expressed throughout the horizontal cells or more specifically at the terminals. {ECO:0000269|PubMed:12115694}.
Sequence
Sequence length 525
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Synaptic vesicle cycle
Retrograde endocannabinoid signaling
GABAergic synapse
Morphine addiction
Nicotine addiction
  Transport of inorganic cations/anions and amino acids/oligopeptides
GABA synthesis, release, reuptake and degradation
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
17
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)
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession Evidence Score
Developmental and epileptic encephalopathy 114 Likely pathogenic; Pathogenic rs2145650130, rs2145650002 RCV003989131
RCV003989157
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Generalized epilepsy with febrile seizures plus Likely pathogenic; Pathogenic rs2084284179, rs2084286998 RCV001260921
RCV001260920
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Generalized epilepsy with febrile seizures plus, type 12 Likely pathogenic; Pathogenic rs2084284179, rs2084286998 RCV003985020
RCV003985019
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Intellectual disability Likely pathogenic rs2145650002, rs2145650130 RCV001800257
RCV001800258
★★★★☆
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
ANOREXIA NERVOSA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
EARLY INFANTILE DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY Orphanet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
EARLY INFANTILE EPILEPTIC ENCEPHALOPATHY WITH SUPPRESSION BURSTS Disgenet
★★☆☆☆
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
Alzheimer Disease Alzheimer disease Pubtator 39650656 Associate
★☆☆☆☆
Found in Text Mining only
Anxiety Anxiety Disorder BEFREE 28129110
★☆☆☆☆
Found in Text Mining only
Anxiety Disorders Anxiety Disorder BEFREE 28129110
★☆☆☆☆
Found in Text Mining only
Autism Spectrum Disorders Autism Spectrum Disorder BEFREE 31133774
★☆☆☆☆
Found in Text Mining only
Congenital exomphalos Congenital Exomphalos BEFREE 25027639
★☆☆☆☆
Found in Text Mining only
Cystitis Cystitis BEFREE 28885452
★☆☆☆☆
Found in Text Mining only
Dementia Dementia Pubtator 29343737 Associate
★☆☆☆☆
Found in Text Mining only
Epilepsy Epilepsy BEFREE 17711980
★☆☆☆☆
Found in Text Mining only
Epilepsy Idiopathic Generalized Epilepsy Pubtator 34038384 Associate
★☆☆☆☆
Found in Text Mining only
Generalized Epilepsy With Febrile Seizures Plus Type 1 Generalized epilepsy with febrile seizures plus Pubtator 34038384 Associate
★☆☆☆☆
Found in Text Mining only