GlyCosmos Portal

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GO Term	Evidence Code	PMID
fibroblast growth factor binding	IBA IPI	18829467
fibroblast growth factor receptor binding	IBA
vitamin D binding	IEA
hormone activity	IEA
beta-glucosidase activity	TAS	9363890

GO Hierarchy

molecular function

catalytic activity [inference]

hydrolase activity [inference]

hydrolase activity, acting on glycosyl bonds [inference]

hydrolase activity, hydrolyzing O-glycosyl compounds [inference]

beta-glucuronidase activity

glucosidase activity [inference]

beta-glucosidase activity

binding [inference]

protein binding [inference]

signaling receptor binding [inference]

receptor ligand activity [inference]

hormone activity

growth factor receptor binding [inference]

fibroblast growth factor receptor binding

growth factor binding [inference]

fibroblast growth factor binding

lipid binding [inference]

steroid binding [inference]

vitamin D binding

small molecule binding [inference]

vitamin binding [inference]

vitamin D binding

organic cyclic compound binding [inference]

steroid binding [inference]

vitamin D binding

molecular function regulator activity [inference]

signaling receptor regulator activity [inference]

signaling receptor activator activity [inference]

receptor ligand activity [inference]

hormone activity

molecular function activator activity [inference]

signaling receptor activator activity [inference]

receptor ligand activity [inference]

hormone activity

Gene Ontology information from NCBI Gene and UniProt.

OrthoDB (Group)

Group level

Eukaryota

Group Name

BETA-GLUCOSIDASE

Functional Category

E: Amino acid transport and metabolism
M: Cell wall/membrane/envelope biogenesis
T: Signal transduction mechanisms

Displaying **all 3** entries
InterPro
Glycoside hydrolase family 1
Glycoside hydrolase superfamily
Glycosyl hydrolases family 1, N-terminal conserved site

KEGG BRITE Database

Orthology

K14756

Name

klotho [EC:3.2.1.31]

References

Rhea

RHEA:17633

H₂O + a β-D-glucuronoside

an alcohol + D-glucuronate

Enzyme

3.2.1.31

PMID

Disease

The Human Phenotype Ontology

Displaying entries **1 - 10** of 14 in total

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HPO ID	HPO Term
HP:0000007	Autosomal recessive inheritance
HP:0000103	Polyuria
HP:0000787	Nephrolithiasis
HP:0000938	Osteopenia
HP:0001959	Polydipsia
HP:0002315	Headache
HP:0002514	Cerebral calcification
HP:0002905	Hyperphosphatemia
HP:0003072	Hypercalcemia
HP:0003165	Elevated circulating parathyroid hormone level

Displaying 1 entry
Disease ID	Disease Name
OMIM:617994	tumoral calcinosis, hyperphosphatemic, familial, 3

PubChem Disease

GHR Health Conditions

MedGen Diseases

Tumoral calcinosis, hyperphosphatemic, familial, 3

OMIM Phenotypes

TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 3; HFTC3

KEGG Diseases

Familial tumoral calcinosis

Gene-Disease-Co-Occurrences-in-Literature (PubChem)

Ortholog

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Species	Gene ID	OrthoDB	Alliance of Genome Resources	Orthologous MAtrix
Mus musculus	16591		MGI:1101771	MOUSE44713
Drosophila melanogaster	39872		FB:FBgn0036659
Rattus norvegicus	83504		RGD:620396	RATNO06192
Caenorhabditis elegans	177557		WB:WBGene00016848
Caenorhabditis elegans	184000		WB:WBGene00017103
Pan troglodytes	467257	9598_0:003896		PANTR07571
Danio rerio	562316		ZFIN:ZDB-GENE-110221-1	DANRE00808
Macaca mulatta	714042			MACMU17091
Bos taurus	784635			BOVIN03796
Equus caballus	100064836			HORSE12565

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

LM-GlycoRepo

All Resources

Other Information

Tools

Search Tools

Summary

External Links

Annotation

OrthoDB (Group)

KEGG BRITE Database

PubChem Disease

International Collaboration

Acknowledgements