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Gene

SLC35B2

solute carrier family 35 member B2

Summary

Cytogenetic location
6p21.1
Coordinates
Chromosome 6: 44,254,101–44,257,528 (GRCh38)
Exons
4 exons across 3.4 kb
Protein
432 amino acids
Also known as
UGTrel4
MANE Select transcript
ENST00000393812.4NM_178148.4
Locus type
gene with protein product
  • Very high
  • Confident
  • Low
  • Very low

Reference genomeGRCh38

Positions on gene and variant pages follow this choice, in this browser.

Curated reports relevant to this gene

No Genome Test report reads SLC35B2 yet. The test sequences your whole genome, so your data includes it all the same.

How SLC35B2 is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
Chromosome 6, with a bracket where SLC35B2 sits. SLC35B2 and 15 genes near it on chromosome 6, from 43,755,815 to 44,755,814.Chromosome 66p21.1p25.3p25.2p25.1p24.3p24.2p24.1p23p22.3p22.2p22.1p21.33p21.32p21.31p21.2p21.1p12.3p12.2p12.1p11.2p11.1q11.1q11.2q12q13q14.1q14.2q14.3q15q16.1q16.2q16.3q21q22.1q22.2q22.31q22.32q22.33q23.1q23.2q23.3q24.1q24.2q24.3q25.1q25.2q25.3q26q2743.8 Mb44 Mb44.2 Mb44.4 Mb44.6 MbVEGFA: 43,770,184–43,786,487, forward strandVEGFALINC03040: 44,000,580–44,007,830, forward strandLINC03040MRPL14: 44,078,275–44,134,339, reverse strandMRPL14TMEM63B: 44,126,614–44,155,520, forward strandTMEM63BCAPN11: 44,158,811–44,184,401, forward strandCAPN11MYMX: 44,192,822–44,218,236, forward strandMYMXSLC29A1: 44,219,245–44,243,425, forward strandSLC29A1HSP90AB1: 44,237,395–44,253,888, forward strandHSP90AB1SLC35B2: 44,254,101–44,257,528, reverse strandSLC35B2NFKBIE: 44,258,166–44,265,788, reverse strandNFKBIETMEM151B: 44,270,450–44,307,506, forward strand: 44,273,194–44,378,957, forward strandDRC5: 44,278,718–44,297,725, reverse strandDRC5AARS2: 44,298,726–44,313,376, reverse strandSPATS1: 44,342,650–44,380,179, forward strandSPATS1CDC5L: 44,387,547–44,450,924, forward strandCDC5LDiagram of SLC35B2: 4 exons on the reverse strand of chromosome 6Exon 4: 2 known disease-causing sitesExon 4: 44,254,101–44,255,644, 1,544 basesExon 3: 44,256,342–44,256,496, 155 basesExon 2: 44,256,685–44,256,878, 194 basesExon 1: 44,257,400–44,257,528, 129 bases43215′3′

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 2 kb of the gene's 3.4 kb; 1,299 of those bases code for the protein.

How a genome test reads SLC35B2

2

positions in SLC35B2 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 3.4 kb of SLC35B2, introns included, not only the 2 kb of exons.

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.
  • 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

APA

Dante Labs. (n.d.). SLC35B2 gene: solute carrier family 35 member B2. Retrieved 17 October 2026, from https://dantelabs.com/genes/slc35b2

Vancouver

Dante Labs. SLC35B2 gene: solute carrier family 35 member B2 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/slc35b2

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