Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
23443
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 35 member A3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC35A3
Synonyms (NCBI Gene) Gene synonyms aliases
AMRS
Disease Acronyms (UniProt) Disease acronyms from UniProt database
AMRS
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1p21.2
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a UDP-N-acetylglucosamine transporter found in the golgi apparatus membrane. In cattle, a missense mutation in this gene causes complex vertebral malformation. Alternative splicing results in multiple transcript variants. [provided by Re
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs141952252 A>G Pathogenic Intron variant, coding sequence variant, missense variant
rs398122524 C>T Pathogenic Coding sequence variant, stop gained
rs866803539 ->A Pathogenic Coding sequence variant, intron variant, frameshift variant
rs1570615526 ->T Pathogenic Splice donor variant
rs1570625903 ->AG Pathogenic Coding sequence variant, frameshift variant, intron variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT019858 hsa-miR-375 Microarray 20215506
MIRT699367 hsa-miR-508-5p HITS-CLIP 23313552
MIRT699366 hsa-miR-383-3p HITS-CLIP 23313552
MIRT699365 hsa-miR-6849-3p HITS-CLIP 23313552
MIRT699364 hsa-miR-1292-3p HITS-CLIP 23313552
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane TAS
GO:0005459 Function UDP-galactose transmembrane transporter activity IBA 21873635
GO:0005462 Function UDP-N-acetylglucosamine transmembrane transporter activity TAS
GO:0005515 Function Protein binding IPI 23089177
GO:0005794 Component Golgi apparatus TAS 10393322
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
605632 11023 ENSG00000117620
Protein
UniProt ID Q9Y2D2
Protein name UDP-N-acetylglucosamine transporter (Golgi UDP-GlcNAc transporter) (Solute carrier family 35 member A3)
Protein function Transports diphosphate-N-acetylglucosamine (UDP-GlcNAc) from the cytosol into the lumen of the Golgi apparatus, functioning as an antiporter that exchanges UDP-N-acetyl-alpha-D-glucosamine for UMP (PubMed:10393322). May supply UDP-GlcNAc as subs
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04142 Nuc_sug_transp 1 313 Nucleotide-sugar transporter Family
Sequence
Sequence length 325
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Defective SLC35A3 causes arthrogryposis, mental retardation, and seizures (AMRS)
Transport of nucleotide sugars
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Arthrogryposis multiplex congenita Arthrogryposis rs1586285494, rs80358233, rs137853305, rs1559154278, rs398124167, rs398124172, rs587780399, rs786204576, rs786204430, rs769345284, rs749355583, rs793888524, rs793888525, rs878854368, rs555445835
View all (138 more)
Autism spectrum disorder-epilepsy-arthrogryposis syndrome Autism spectrum disorder-epilepsy-arthrogryposis syndrome rs398122524, rs141952252, rs1553201582, rs866803539, rs1570625903, rs1570615526, rs1660027548
Autism Autistic behavior rs121964908, rs62643608, rs181327458, rs797046134, rs869312704, rs1555013332, rs876657679, rs1057518999, rs1057518658, rs771827120, rs1555187899, rs773080572, rs753871454, rs1684130791, rs1684180699
View all (8 more)
Developmental delay Global developmental delay rs28941770, rs199469464, rs281865469, rs143747297, rs398123009, rs587777428, rs786205133, rs606231459, rs797044854, rs797045027, rs864309504, rs878853160, rs886039902, rs886042046, rs886041291
View all (32 more)
Associations from Text Mining
Disease Name Relationship Type References
Colorectal Neoplasms Associate 38172565
Congenital Disorders of Glycosylation Associate 29869806
Hypoxia Associate 33418078
Neoplasms Associate 30914738, 38172565