GLB1L3
Beta-galactosidase-1-like protein 3
Also known as: FLJ90231, GLBL3_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8NCI6
- Gene
- GLB1L3
- Ensembl
- ENSG00000166105
- Chromosome
- 11
- Canonical length
- 653 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
Predicted to enable beta-galactosidase activity. Predicted to be involved in galactose catabolic process. Predicted to be active in vacuole. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
653 residues, UniProt reviewed canonical sequence.
>Q8NCI6|GLB1L3
1 MKSPPLLSPC LSWKRMAGIF FLPFISSGFA PRFKQEENFM LGRAHPSQPR FNWSHLTPLE
61 LKNRSVGLGT ESTGRGKPHF TLEGHKFLIF GGSIHYFRVP REYWRDRLLK LKACGFNTVT
121 TYVPWNLHEP ERGKFDFSGN LDLEAFVLMA AEIGLWVILR PGRYICSEMD LGGLPSWLLQ
181 DPRLLLRTTN KSFIEAVEKY FDHLIPRVIP LQYRQAGPVI AVQVENEYGS FNKDKTYMPY
241 LHKALLRRGI VELLLTSDGE KHVLSGHTKG VLAAINLQKL HQDTFNQLHK VQRDKPLLIM
301 EYWVGWFDRW GDKHHVKDAK EVEHAVSEFI KYEISFNVYM FHGGTNFGFM NGATYFGKHS
361 GIVTSYDYDA VLTEAGDYTE KYLKLQKLFQ SVSATPLPRV PKLPPKAVYP PVRPSLYLPL
421 WDALSYLNEP VRSRQPVNME NLPINNGSGQ SYGLVLYEKS ICSGGRLRAH AHDVAQVFLD
481 ETMIGILNEN NKDLHIPELR DCRYLRILVE NQGRVNFSWQ IQNEQKGITG SVSINNSSLE
541 GFTIYSLEMK MSFFERLRSA TWKPVPDSHQ GPAFYCGTLK AGPSPKDTFL SLLNWNYGFV
601 FINGRNLGRY WNIGPQKTLY LPGVWLHPED NEVILFEKMM SGSDIKSTDK PTLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against GLB1L3 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
- Unknown
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.23
- Highest tissue expression
- 7.5 nTPM
Expression across tissuesHPA
Tissue
- prostate: 7.5 nTPM
- seminal vesicle: 4.1 nTPM
- cerebellum: 2.7 nTPM
- cerebral cortex: 2.2 nTPM
- skin: 2.2 nTPM
- salivary gland: 1.9 nTPM
Single-cell type
- brain excitatory neurons: 34 nCPM
- retinal ganglion cells: 31 nCPM
- brain inhibitory neurons: 30 nCPM
- undifferentiated spermatogonia: 25 nCPM
- other brain neurons: 22 nCPM
- differentiating spermatogonia: 21 nCPM
Immune cell
- memory CD4 T-cell: 3.1 nTPM
- naive CD4 T-cell: 2.4 nTPM
- memory CD8 T-cell: 1.9 nTPM
- naive CD8 T-cell: 1.9 nTPM
- T-reg: 1.5 nTPM
- gdT-cell: 1.2 nTPM
Brain region
- cerebral cortex: 17 nTPM
- cerebellum: 12 nTPM
- white matter: 9.5 nTPM
- basal ganglia: 9.1 nTPM
- pons: 8.3 nTPM
- hippocampal formation: 7.5 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)
- 1.21
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.04
- DepMap mean gene effect
- 0.08
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Glycoside hydrolase, family 35
- Galactose-binding-like domain superfamily
- Glycoside hydrolase superfamily
- Beta-galactosidase 1-like
- Glycoside hydrolase 35, catalytic domain
- Beta-galactosidase 1-like , first all-beta domain
- Beta-galactosidase, galactose-binding domain
- Glycosyl hydrolases family 35
- Beta-galactosidase, first all-beta domain
- Beta-galactosidase, galactose-binding domain
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads GLB1L3 as an antibody target. Whether an autoantibody or antibody against GLB1L3 could matter depends on whether native GLB1L3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GLB1L3 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 GLB1L3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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