Version 5.4
Homo sapiens Gene: GLB1L
Summary
InnateDB Gene IDBG-81422.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol GLB1L
Gene Name galactosidase, beta 1-like
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000163521
Encoded Proteins
IDBP-81424
galactosidase, beta 1-like
IDBP-246370
galactosidase, beta 1-like
IDBP-293012
galactosidase, beta 1-like
IDBP-389035
galactosidase, beta 1-like
IDBP-389036
galactosidase, beta 1-like
IDBP-389037
galactosidase, beta 1-like
IDBP-389038
galactosidase, beta 1-like
IDBP-389039
galactosidase, beta 1-like
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary Currently no Entrez Summary Available. You might want to check the Summary Sections of the Orthologs.
Gene Information
Type Protein coding
Genomic Location Chromosome 2:219236606-219245478
Strand Reverse strand
Band q35
Transcripts
ENST00000295759 ENSP00000295759
ENST00000392089 ENSP00000375939
ENST00000409640 ENSP00000386354
ENST00000447002 ENSP00000396263
ENST00000440853 ENSP00000387703
ENST00000428427 ENSP00000400738
ENST00000424620 ENSP00000404698
ENST00000432839 ENSP00000392018
ENST00000497855
ENST00000471516
ENST00000459951
ENST00000467548
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
Experimentally validated
Total 2 [view]
Protein-Protein 2 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0004553 hydrolase activity, hydrolyzing O-glycosyl compounds
GO:0004565 beta-galactosidase activity
Biological Process
GO:0005975 carbohydrate metabolic process
Cellular Component
GO:0005576 extracellular region
GO:0009341 beta-galactosidase complex
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
ENSMUSG00000026200
View Gene Order
ENSBTAG00000020611
Not yet available
Pathways
NETPATH
REACTOME
REACT_116105
Glycosphingolipid metabolism pathway
REACT_121313
Keratan sulfate degradation pathway
REACT_120752
HS-GAG degradation pathway
REACT_19323
Sphingolipid metabolism pathway
REACT_22258
Metabolism of lipids and lipoproteins pathway
REACT_147853
Mucopolysaccharidoses pathway
REACT_200783
Myoclonic epilepsy of Lafora pathway
REACT_267711
Defective B4GALT7 causes EDS, progeroid type pathway
REACT_267713
Defective CHST6 causes MCDC1 pathway
REACT_121288
Keratan sulfate/keratin metabolism pathway
REACT_147719
MPS VI - Maroteaux-Lamy syndrome pathway
REACT_267645
Defective PAPSS2 causes SEMD-PA pathway
REACT_474
Metabolism of carbohydrates pathway
REACT_147749
MPS IIID - Sanfilippo syndrome D pathway
REACT_267662
Defective SLC26A2 causes chondrodysplasias pathway
REACT_147739
MPS IX - Natowicz syndrome pathway
REACT_267674
Defective EXT1 causes exostoses 1, TRPS2 and CHDS pathway
REACT_267642
Defective CHST14 causes EDS, musculocontractural type pathway
REACT_121314
Heparan sulfate/heparin (HS-GAG) metabolism pathway
REACT_147798
MPS IV - Morquio syndrome B pathway
REACT_267659
Defective B3GAT3 causes JDSSDHD pathway
REACT_267708
Defective CHST3 causes SEDCJD pathway
REACT_147825
MPS IV - Morquio syndrome A pathway
REACT_267654
Defective EXT2 causes exostoses 2 pathway
REACT_267707
Diseases associated with glycosaminoglycan metabolism pathway
REACT_147734
MPS II - Hunter syndrome pathway
REACT_267635
Defective B4GALT1 causes B4GALT1-CDG (CDG-2d) pathway
REACT_121315
Glycosaminoglycan metabolism pathway
REACT_267705
Diseases of glycosylation pathway
REACT_147759
MPS VII - Sly syndrome pathway
REACT_267682
Defective CHSY1 causes TPBS pathway
REACT_111217
Metabolism pathway
REACT_147857
MPS I - Hurler syndrome pathway
REACT_147753
MPS IIIA - Sanfilippo syndrome A pathway
REACT_147860
MPS IIIC - Sanfilippo syndrome C pathway
REACT_116125
Disease pathway
REACT_200833
Glycogen storage diseases pathway
REACT_147788
MPS IIIB - Sanfilippo syndrome B pathway
KEGG
INOH
PID NCI
Cross-References
SwissProt Q6UWU2
TrEMBL A0A024R439 C9J1Y9 C9JE41
UniProt Splice Variant
Entrez Gene 79411
UniGene Hs.181173
RefSeq NM_001286423 NM_001286427 NM_024506 XM_005246850 XM_005246851
HUGO HGNC:28129
OMIM
CCDS CCDS2437 CCDS74657
HPRD 11004
IMGT
EMBL AC068946 AK055098 AY358639 CH471063
GenPept AAQ89002 BAB70855 EAW70711 EAW70712 EAW70713
RNA Seq Atlas 79411

If you use InnateDB for your research, please cite the following publication:

Breuer et al., InnateDB: systems biology of innate immunity and beyond - recent updates and continuing curation. Nucl. Acids Res. (2013) 41 (D1) 

InnateDB is being developed jointly by the Brinkman Laboratory (Simon Fraser University, British Columbia, Canada), the Hancock Laboratory (University of British Columbia, Vancouver, British Columbia) and the Lynn EMBL Australia Group (South Australian Health & Medical Research Institute and Flinders University, Adelaide, Australia).

Funding is currently provided by Allergen and EMBL Australia. Previous funding has been provided by Genome Canada, the Foundation for the National Institutes of Health through the Grand Challenges in Global Health initiative and by Teagasc. InnateDB curated interactions are licensed under the Design Science License. All other data is licensed under the terms of the originating database. Contact: innatedb-mail@sfu.ca