Gene Gene information from NCBI Gene database.
Entrez ID 126792
Gene name Beta-1,3-galactosyltransferase 6
Gene symbol B3GALT6
Synonyms (NCBI Gene)
ALGAZEDSP2EDSSPD2SEMDJL1beta3GalT6
Chromosome 1
Chromosome location 1p36.33
Summary The enzyme encoded by this intronless gene is a beta-1,3-galactosyltransferase found in the medial Golgi apparatus, where it catalyzes the transfer of galactose from UDP-galactose to substrates containing a terminal beta-linked galactose moiety. The encod
miRNA miRNA information provided by mirtarbase database.
107
miRTarBase ID miRNA Experiments Reference
MIRT813022 hsa-miR-1271 CLIP-seq
MIRT813023 hsa-miR-129-5p CLIP-seq
MIRT813024 hsa-miR-1343 CLIP-seq
MIRT813025 hsa-miR-141 CLIP-seq
MIRT813026 hsa-miR-1539 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
30
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane IBA
GO:0000139 Component Golgi membrane TAS
GO:0005794 Component Golgi apparatus IEA
GO:0005794 Component Golgi apparatus IEA
GO:0005794 Component Golgi apparatus IMP 29443383
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
615291 17978 ENSG00000176022
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96L58
Protein name Beta-1,3-galactosyltransferase 6 (Beta-1,3-GalTase 6) (Beta3Gal-T6) (Beta3GalT6) (EC 2.4.1.134) (GAG GalTII) (Galactosyltransferase II) (Galactosylxylosylprotein 3-beta-galactosyltransferase) (UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6)
Protein function Beta-1,3-galactosyltransferase that transfers galactose from UDP-galactose to substrates with a terminal beta-linked galactose residue. Has a preference for galactose-beta-1,4-xylose that is found in the linker region of glycosaminoglycans, such
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01762 Galactosyl_T 71 260 Galactosyltransferase Family
Tissue specificity TISSUE SPECIFICITY: Ubiquitous. {ECO:0000269|PubMed:11551958}.
Sequence
MKLLRRAWRRRAALGLGTLALCGAALLYLARCAAEPGDPRAMSGRSPPPPAPARAAAFLA
VLVASAPRAAERRSVIRSTWLARRGAPGDVWARFAVGTAGLGAEERRALEREQARHGDLL
LLPALRDAYENLTAKVLAMLAWLDEHVAFEFVLKADDDSFARLDALLAELRAREPARRRR
LYWGFFSGRGRVKPGGRWREAAWQLCDYYLPYALGGGYVLSADLVHYLRLSRDYLRAWHS
EDVSLGAWLAPVDVQREHDP
RFDTEYRSRGCSNQYLVTHKQSLEDMLEKHATLAREGRLC
KREVQLRLSYVYDWSAPPSQCCQRREGIP
Sequence length 329
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
595
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Al-Gazali syndrome Pathogenic rs786200938, rs1360531002, rs763080896 RCV004821343
RCV001089597
RCV001089599
B3GALT6-related disorder Likely pathogenic; Pathogenic rs778123798, rs786200938 RCV004754826
RCV003944971
Ehlers-Danlos syndrome, spondylodysplastic type, 2 Likely pathogenic; Pathogenic rs778123798, rs969701761, rs2521960362, rs1638540007, rs786200938, rs1553151294, rs397514720, rs397514721, rs533071750, rs1638566519, rs1638539773 RCV002010337
RCV001378837
RCV002007594
RCV003074887
RCV003780941
RCV004821343
RCV001090033
RCV001853073
RCV001853074
RCV000054397
RCV000054398
RCV001290345
RCV001290346
Spondyloepimetaphyseal dysplasia with joint laxity Likely pathogenic; Pathogenic rs778123798, rs969701761, rs2521960362, rs1638540007, rs786200938, rs397514720, rs397514721 RCV002010337
RCV001378837
RCV002007594
RCV003074887
RCV003780941
RCV001853073
RCV001853074
RCV003764726
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Carcinoma Hepatocellular Associate 30168613
Connective Tissue Diseases Associate 23664117, 23664118
Contracture Associate 23664118
Ehlers Danlos Syndrome Associate 23664117, 23664118, 25331875
Ehlers Danlos syndrome type 3 Associate 28882145, 31614862
Glaucoma Associate 26086840
Growth Disorders Associate 31614862
HEM dysplasia Associate 23664117, 31614862
Intellectual Disability Associate 23664118
Joint Diseases Associate 23664118