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
galactosidase, beta 1-like
galactosidase, beta 1-like
galactosidase, beta 1-like
galactosidase, beta 1-like
galactosidase, beta 1-like
galactosidase, beta 1-like
galactosidase, beta 1-like
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
Method
Confidence
Comments
SSD Ortholog
Ortholog supports species divergence
Not yet available
SSD Ortholog
Ortholog supports species divergence
Pathways
NETPATH
REACTOME
Sphingolipid metabolism pathway
Metabolism of lipids and lipoproteins pathway
Mucopolysaccharidoses pathway
HS-GAG degradation pathway
Myoclonic epilepsy of Lafora pathway
Defective B4GALT7 causes EDS, progeroid type pathway
Defective CHST6 causes MCDC1 pathway
Keratan sulfate/keratin metabolism pathway
MPS VI - Maroteaux-Lamy syndrome pathway
Defective PAPSS2 causes SEMD-PA pathway
Metabolism of carbohydrates pathway
MPS IIID - Sanfilippo syndrome D pathway
Defective SLC26A2 causes chondrodysplasias pathway
MPS IX - Natowicz syndrome pathway
Defective EXT1 causes exostoses 1, TRPS2 and CHDS pathway
Defective CHST14 causes EDS, musculocontractural type pathway
Heparan sulfate/heparin (HS-GAG) metabolism pathway
MPS IV - Morquio syndrome B pathway
Defective B3GAT3 causes JDSSDHD pathway
Keratan sulfate degradation pathway
Glycosphingolipid metabolism pathway
Defective CHST3 causes SEDCJD pathway
MPS IV - Morquio syndrome A pathway
Defective EXT2 causes exostoses 2 pathway
Diseases associated with glycosaminoglycan metabolism pathway
MPS II - Hunter syndrome pathway
Defective B4GALT1 causes B4GALT1-CDG (CDG-2d) pathway
Glycosaminoglycan metabolism pathway
Diseases of glycosylation pathway
MPS VII - Sly syndrome pathway
Defective CHSY1 causes TPBS pathway
Metabolism pathway
MPS I - Hurler syndrome pathway
MPS IIIA - Sanfilippo syndrome A pathway
MPS IIIC - Sanfilippo syndrome C pathway
Disease pathway
Glycogen storage diseases pathway
MPS IIIB - Sanfilippo syndrome B pathway
KEGG
INOH
PID BIOCARTA
PID NCI
Cross-References
SwissProt Q6UWU2
TrEMBL A0A024R439 C9J1Y9 C9JE41 F8WCT5
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
IMGT
EMBL AC068946 AK055098 AY358639 CH471063
GenPept AAQ89002 BAB70855 EAW70711 EAW70712 EAW70713
RNA Seq Atlas 79411