GlyCosmos Portal

Displaying entries **1 - 5** of 7 in total

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GO Term	Evidence Code	PMID
kinase activity	IEA
magnesium ion binding	IEA
protein homodimerization activity	IPI	16939420
ATP binding	IBA IDA	16939420
protein binding	IPI	16189514 25416956 25910212 26496610 28514442 29892012 31515488 32296183 32814053

GO Hierarchy

molecular function

catalytic activity [inference]

transferase activity [inference]

transferase activity, transferring phosphorus-containing groups [inference]

kinase activity

diphosphotransferase activity [inference]

ribose phosphate diphosphokinase activity

binding [inference]

protein binding

identical protein binding

protein homodimerization activity

protein dimerization activity [inference]

protein homodimerization activity

small molecule binding [inference]

heterocyclic compound binding [inference]

nucleotide binding [inference]

purine nucleotide binding [inference]

adenyl nucleotide binding [inference]

adenyl ribonucleotide binding [inference]

ATP binding

purine ribonucleotide binding [inference]

adenyl ribonucleotide binding [inference]

ATP binding

ribonucleotide binding [inference]

purine ribonucleotide binding [inference]

adenyl ribonucleotide binding [inference]

ATP binding

ion binding [inference]

anion binding [inference]

purine ribonucleoside triphosphate binding [inference]

ATP binding

cation binding [inference]

metal ion binding [inference]

magnesium ion binding

organic cyclic compound binding [inference]

nucleoside phosphate binding [inference]

nucleotide binding [inference]

purine nucleotide binding [inference]

adenyl nucleotide binding [inference]

adenyl ribonucleotide binding [inference]

ATP binding

purine ribonucleotide binding [inference]

adenyl ribonucleotide binding [inference]

ATP binding

ribonucleotide binding [inference]

purine ribonucleotide binding [inference]

adenyl ribonucleotide binding [inference]

ATP binding

purine ribonucleoside triphosphate binding [inference]

ATP binding

carbohydrate derivative binding [inference]

ribonucleotide binding [inference]

purine ribonucleotide binding [inference]

adenyl ribonucleotide binding [inference]

ATP binding

Gene Ontology information from NCBI Gene and UniProt.

Human Protein Atlas

ENSG00000147224

Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.

Data available from v23.0.proteinatlas.org. Image credit: Human Protein Atlas

KEGG BRITE Database

Orthology

K00948

Name

ribose-phosphate pyrophosphokinase [EC:2.7.6.1]

References

Rhea

RHEA:15609

ATP + D-ribose 5-phosphate

H⁺ + AMP + 5-phospho-α-D-ribose 1-diphosphate

Enzyme

2.7.6.1

PMID

Disease

Disease Ontology

Displaying entries **31 - 40** of **150** in total

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DO ID	Disease Name	Source
DOID:0110167	Charcot-Marie-Tooth disease axonal type 2K	DisGeNET
DOID:0110168	Charcot-Marie-Tooth disease type 2Y	DisGeNET
DOID:0110169	Charcot-Marie-Tooth disease axonal type 2P	DisGeNET
DOID:0110170	Charcot-Marie-Tooth disease axonal type 2Q	DisGeNET
DOID:0110173	Charcot-Marie-Tooth disease axonal type 2U	DisGeNET
DOID:0110174	Charcot-Marie-Tooth disease axonal type 2L	DisGeNET
DOID:0110175	Charcot-Marie-Tooth disease axonal type 2O	DisGeNET
DOID:0110177	Charcot-Marie-Tooth disease axonal type 2N	DisGeNET
DOID:0110179	Charcot-Marie-Tooth disease type 2B2	DisGeNET
DOID:0110182	Charcot-Marie-Tooth disease axonal type 2C	DisGeNET

The Human Phenotype Ontology

Displaying entries **1 - 10** of **135** in total

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HPO ID	HPO Term
HP:0000028	Cryptorchidism
HP:0000047	Hypospadias
HP:0000083	Renal insufficiency
HP:0000154	Wide mouth
HP:0000218	High palate
HP:0000268	Dolichocephaly
HP:0000286	Epicanthus
HP:0000316	Hypertelorism
HP:0000325	Triangular face
HP:0000365	Hearing impairment

Displaying **all 9** entries
Disease ID	Disease Name
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-diabetes insipidus syndrome
OMIM:311070	Charcot-Marie-Tooth disease X-linked recessive 5
ORPHA:411543	severe phosphoribosylpyrophosphate synthetase superactivity
OMIM:301835	Arts syndrome
OMIM:304500	hearing loss, X-linked 1
ORPHA:1187	Arts syndrome
ORPHA:411536	mild phosphoribosylpyrophosphate synthetase superactivity
OMIM:300661	phosphoribosylpyrophosphate synthetase superactivity
ORPHA:99014	Charcot-Marie-Tooth disease X-linked recessive 5

PubChem Disease

GHR Health Conditions

MedGen Diseases

OMIM Phenotypes

KEGG Diseases

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

Ortholog

Displaying entries **11 - 20** of **101** in total

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Species	Gene ID	Orthologous MAtrix
Electrophorus electricus	113568088	ELEEL15560
Electrophorus electricus	113574179	ELEEL15560
Salmo salar	100195336	SALSA31811
Salmo salar	106567858	SALSA31811
Salmo salar	106604323	SALSA124598
Salmo salar	106612209	SALSA124598
Salmo trutta	115148987	SALTR104494
Salmo trutta	115154449	SALTR104494
Salmo trutta	115167895	SALTR44102
Salmo trutta	115205660	SALTR110383

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

Summary

External Links

Annotation

KEGG BRITE Database

PubChem Disease

International Collaboration

Acknowledgements