Gene
B4GALT7
beta-1,4-galactosyltransferase 7
- HGNC 930↗(opens in a new tab)
- Ensembl gene ENSG00000027847↗(opens in a new tab)
- NCBI Gene 11285↗(opens in a new tab)
Summary
- Cytogenetic location
- 5q35.3
- Coordinates
- Chromosome 5: 177,600,132–177,610,330 (GRCh38)
- Exons
- 6 exons across 10.2 kb
- Protein
- 327 amino acids
- Also known as
- XGALT-1, beta4Gal-T7
- MANE Select transcript
- ENST00000029410.10NM_007255.3
- 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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Ehlers-Danlos Syndrome
- ClinGen rates the link definitive
- 5 GenCC submitters rate it definitive or strong
How B4GALT7 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
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 1.7 kb of the gene's 10.2 kb; 984 of those bases code for the protein.
How a genome test reads B4GALT7
25
positions in B4GALT7 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 10.2 kb of B4GALT7, introns included, not only the 1.7 kb of exons.
Genes linked to the same conditions
- ADAMTS2ADAM metallopeptidase with thrombospondin type 1 motif 2Shares 1 condition
- AEBP1AE binding protein 1Shares 1 condition
- B3GALT6beta-1,3-galactosyltransferase 6Shares 1 condition
- C1Rcomplement C1rShares 1 condition
- C1Scomplement C1sShares 1 condition
- CHST14carbohydrate sulfotransferase 14Shares 1 condition
- COL12A1collagen type XII alpha 1 chainShares 1 condition
- COL1A1collagen type I alpha 1 chainShares 1 condition
- COL1A2collagen type I alpha 2 chainShares 1 condition
- COL3A1collagen type III alpha 1 chainShares 1 condition
- COL5A1collagen type V alpha 1 chainShares 1 condition
- COL5A2collagen type V alpha 2 chainShares 1 condition
Traits linked to B4GALT7
The Human Phenotype Ontology lists these as features of the rare conditions B4GALT7 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.). B4GALT7 gene: beta-1,4-galactosyltransferase 7. Retrieved 17 October 2026, from https://dantelabs.com/genes/b4galt7
Dante Labs. B4GALT7 gene: beta-1,4-galactosyltransferase 7 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/b4galt7
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