B3GNTL1
Queuosine-tRNA galactosyltransferase
Also known as: B3GNT8, QTGAL_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q67FW5
- Gene
- B3GNTL1
- Ensembl
- ENSG00000175711
- Chromosome
- 17
- Canonical length
- 346 aa
- Protein class
- Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoli,Nucleoli fibrillar center,Vesicles
OverviewNCBI Gene
Enables tRNA-queuosine(34) galactosyltransferase activity. Involved in regulation of translation and tRNA modification. Is active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
346 residues, UniProt reviewed canonical sequence.
>Q67FW5|B3GNTL1
1 MQAHVSIILP VHNAEPWLDE CLRSVLQQDF EGTMELSVFN DASKDKSGAI IEKWRVKLED
61 SGVHVIIGGH DSPSPRGVGY AKNQAVAQSS GSYLCFLDSD DVMMPQRVRL QHEAAVQHPS
121 SIIGCRVRRD PPNSTERYTR WINQLTPEQL LTQVFTSNGP TVIMPTWFCS RAWFSHVGPF
181 NEGGQGVPED LLFFYEHLRK GGGVIRVDQS LLLYRHHPQA ATHCVLETTI WTHRVRFLEE
241 QALPRWAAFT IWNAGKQGRR LYRSLTAGSQ RKVVAFCDVD ENKIRKGFYC HEDSQERPKP
301 RIPILHFRAA RPPFVICVKL DLTGGAFEDN LRSLHLQEGQ DFLHFSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against B3GNTL1 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.24
- Highest tissue expression
- 5.8 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 5.8 nTPM
- basal ganglia: 2.9 nTPM
- spleen: 2.7 nTPM
- choroid plexus: 2.6 nTPM
- cerebral cortex: 2.5 nTPM
- hippocampal formation: 2.3 nTPM
Single-cell type
- neutrophils: 42 nCPM
- choroid plexus epithelial cells: 30 nCPM
- late spermatids: 28 nCPM
- oocytes: 28 nCPM
- epididymal principal cells: 27 nCPM
- brain inhibitory neurons: 20 nCPM
Immune cell
- neutrophil: 6.2 nTPM
- T-reg: 1.4 nTPM
- basophil: 1.3 nTPM
- classical monocyte: 1.1 nTPM
- myeloid DC: 1.1 nTPM
- MAIT T-cell: 1 nTPM
Brain region
- choroid plexus: 4.2 nTPM
- white matter: 3.3 nTPM
- cerebral cortex: 2.9 nTPM
- thalamus: 2.8 nTPM
- hippocampal formation: 2.7 nTPM
- basal ganglia: 2.6 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.8
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.02
- DepMap mean gene effect
- 0.04
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
- tRNA-queuosine(34) galactosyltransferase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads B3GNTL1 as an antibody target. Whether an autoantibody or antibody against B3GNTL1 could matter depends on whether native B3GNTL1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
B3GNTL1 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label B3GNTL1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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