solute carrier family 35 member A3

Summary
Gene Symbol
  • SLC35A3
Aliases
  • UDP-N-acetylglucosamine transporter
Organism
Homo sapiens (human)
External Links
NCBI Gene
23443
GGDB ID
HGNC
11023
mRNA
map
  • 1p21
Protein
OMIM
KEGG Gene ID
hsa:23443
PubChem
23443
Alliance of Genome Resources
Annotation
Keyword
  • Alternative splicing
  • Antiport
  • Autism spectrum disorder
  • Disease variant
  • Epilepsy
  • Golgi apparatus
  • Intellectual disability
  • Proteomics identification
  • Reference proteome
  • Sugar transport
  • Transmembrane helix
Proteins
Displaying all 4 entries
UniProt Protein Name
Q9Y2D2
  • Golgi UDP-GlcNAc transporter
  • Solute carrier family 35 member A3
A0A1W2PQL8
  • Golgi UDP-GlcNAc transporter
  • Solute carrier family 35 member A3
A0A1W2PSD1
  • Golgi UDP-GlcNAc transporter
  • Solute carrier family 35 member A3
A0A1W2PRT7
  • Golgi UDP-GlcNAc transporter
  • Solute carrier family 35 member A3
Gene Ontology (GO)
GO Hierarchy
Human Protein Atlas
ENSG00000117620

soft tissue soft tissue blood blood blood blood blood blood blood blood blood blood blood blood blood blood lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node kidney kidney adrenal gland adrenal gland breast breast duodenum stomach small intestine colon rectum appendix esophagus eye eye salivary gland nasopharynx nasopharynx tongue tonsil tonsil tonsil hair skin adipose tissue adipose tissue adipose tissue spinal cord oral mucosa lung lung heart bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus liver pancreas thyroid gland parathyroid gland parathyroid gland parathyroid gland parathyroid gland parathyroid gland spleen gallbladder ductus deferens ductus deferens seminal vesicle seminal vesicle seminal vesicle seminal vesicle testis testis epididymis epididymis brain smooth muscle urinary bladder prostate bone marrow skeletal muscle skeletal muscle skeletal muscle skeletal muscle skeletal muscle thymus thymus cartilage sole of foot sole of foot soft tissue blood blood blood blood blood blood blood blood blood blood blood blood lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node lactating breast lactating breast kidney kidney adrenal gland adrenal gland duodenum stomach small intestine colon rectum appendix esophagus eye eye salivary gland salivary gland salivary gland salivary gland salivary gland salivary gland nasopharynx tongue tonsil tonsil hair skin adipose tissue adipose tissue adipose tissue adipose tissue adipose tissue adipose tissue adipose tissue spinal cord oral mucosa lung lung heart bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus liver pancreas thyroid gland parathyroid gland parathyroid gland parathyroid gland parathyroid gland parathyroid gland spleen gallbladder brain skeletal muscle skeletal muscle skeletal muscle skeletal muscle skeletal muscle thymus thymus smooth muscle urinary bladder vagina ovary ovary fallopian tube fallopian tube endometrium placenta cervix cervix bone marrow cartilage sole of foot sole of foot olfactory region cerebral cortex cerebellum medulla pons midbrain pituitary gland hypothalamus amygdala thalamus choroid plexus choroid plexus corpus callosum basal ganglia substantia nigra dorsal raphe dorsal raphe dorsal raphe dorsal raphe dorsal raphe dorsal raphe caudate hippocampus retina retina

Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.

GlycoGene Database (GGDB)
GGDB ID
gg174
Gene Symbol
  • SLC35A3
Orthologous Gene
KEGG BRITE Database
Orthology
K15272
Name
solute carrier family 35 (UDP-sugar transporter), member A1/2/3
References
Disease
Disease Ontology
Displaying entries 1 - 10 of 21 in total
DO ID Disease Name Source
DOID:0050568 spondylocostal dysostosis
DOID:0060041 autism spectrum disorder
DOID:0060249 scoliosis
DOID:0060823 syndromic X-linked intellectual disability 94
DOID:1059 intellectual disability
DOID:10907 microcephaly
DOID:11832 visual epilepsy
DOID:12721 multiple epiphyseal dysplasia
DOID:12804 mucopolysaccharidosis IV
DOID:12849 autistic disorder
The Human Phenotype Ontology
Displaying entries 1 - 10 of 22 in total
HPO ID HPO Term
HP:0000007 Autosomal recessive inheritance
HP:0000252 Microcephaly
HP:0000308 Microretrognathia
HP:0000729 Autistic behavior
HP:0001249 Intellectual disability
HP:0001256 Intellectual disability, mild
HP:0001263 Global developmental delay
HP:0001290 Generalized hypotonia
HP:0001385 Hip dysplasia
HP:0001765 Hammertoe
Displaying all 2 entries
Disease ID Disease Name
ORPHA:370943
  • autism spectrum disorder - epilepsy - arthrogryposis syndrome
OMIM:615553
  • autism spectrum disorder - epilepsy - arthrogryposis syndrome

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024