Gene
SLC35A3
solute carrier family 35 member A3
- HGNC 11023↗(opens in a new tab)
- Ensembl gene ENSG00000117620↗(opens in a new tab)
- NCBI Gene 23443↗(opens in a new tab)
Summary
- Cytogenetic location
- 1p21.2
- Coordinates
- Chromosome 1: 99,969,996–100,035,634 (GRCh38)
- Exons
- 8 exons across 65.6 kb
- Protein
- 325 amino acids
- MANE Select transcript
- ENST00000533028.8NM_012243.3
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Congenital Disorders of Glycosylation
- Congenital Disorders of Glycosylation (CDG)
One of 98 genes linked to it
A large group of inherited conditions in which sugar chains (glycans) are not correctly built or attached to proteins and lipids, often affecting the brain, liver, blood clotting, growth and many other body systems. Most are autosomal recessive, but some are X-linked or autosomal dominant.
- 3 GenCC submitters rate it definitive or strong
How SLC35A3 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
- Stretches short reads find hard
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 14.3 kb of the gene's 65.6 kb; 978 of those bases code for the protein.
How a genome test reads SLC35A3
51
positions in SLC35A3 where ClinVar classes a change as pathogenic or likely pathogenic
None of them falls in a region short reads find hard.
A whole genome covers all 65.6 kb of SLC35A3, introns included, not only the 14.3 kb of exons.
Genes linked to the same conditions
- A4GALTalpha 1,4-galactosyltransferase (P1PK blood group)Shares 1 condition
- ALG1ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferaseShares 1 condition
- ALG11ALG11 alpha-1,2-mannosyltransferaseShares 1 condition
- ALG12ALG12 alpha-1,6-mannosyltransferaseShares 1 condition
- ALG13ALG13 UDP-N-acetylglucosaminyltransferase subunitShares 1 condition
- ALG14ALG14 UDP-N-acetylglucosaminyltransferase subunitShares 1 condition
- ALG2ALG2 alpha-1,3/1,6-mannosyltransferaseShares 1 condition
- ALG3ALG3 alpha-1,3- mannosyltransferaseShares 1 condition
- ALG6ALG6 alpha-1,3-glucosyltransferaseShares 1 condition
- ALG8ALG8 alpha-1,3-glucosyltransferaseShares 1 condition
- ALG9ALG9 alpha-1,2-mannosyltransferaseShares 1 condition
- ATP6AP1ATPase H+ transporting accessory protein 1Shares 1 condition
Traits linked to SLC35A3
The Human Phenotype Ontology lists these as features of the rare conditions SLC35A3 can cause. Each trait's page lists the other genes linked to it.
External links
Gene records
Transcript
Protein
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
- GenCC and ClinGen, released 2026-10-16: which conditions the gene is linked to, and how strongly.
- The ACMG secondary findings list, SF v3.2.
- ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). SLC35A3 gene: solute carrier family 35 member A3. Retrieved 17 October 2026, from https://dantelabs.com/genes/slc35a3
Dante Labs. SLC35A3 gene: solute carrier family 35 member A3 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/slc35a3
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