GlyCosmos Portal

Displaying **all 4** entries
GO Term	Evidence Code	PMID
dehydrodolichyl diphosphate synthase activity	IDA	28842490
metal ion binding	IEA
protein binding	IPI	15110773 32817466
polyprenyltransferase activity	IDA	25066056

GO Hierarchy

molecular function

catalytic activity [inference]

transferase activity [inference]

transferase activity, transferring alkyl or aryl (other than methyl) groups [inference]

prenyltransferase activity [inference]

binding [inference]

protein binding

ion binding [inference]

cation binding [inference]

metal ion binding

Gene Ontology information from NCBI Gene and UniProt.

Human Protein Atlas

ENSG00000117682

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

K11778

Name

ditrans,polycis-polyprenyl diphosphate synthase [EC:2.5.1.87]

References

Rhea

RHEA:53008

isopentenyl diphosphate + (2E,6E)-farnesyl diphosphate

diphosphate

Enzyme

2.5.1.87

PMID

Disease

Disease Ontology

Displaying entries **1 - 10** of **186** in total

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DO ID	Disease Name	Source
DOID:0060608	microcephalic osteodysplastic primordial dwarfism type I	DisGeNET
DOID:0050569	Seckel syndrome	DisGeNET
DOID:0050572	cone-rod dystrophy	DisGeNET
DOID:0050589	inflammatory bowel disease	DisGeNET DisGeNET
DOID:0050590	severe congenital neutropenia	DisGeNET
DOID:0050591	tooth agenesis	DisGeNET
DOID:0050782	Zollinger-Ellison syndrome	DisGeNET
DOID:0050841	focal hand dystonia	DisGeNET
DOID:0050902	medulloblastoma	DisGeNET
DOID:0060058	lymphoma	DisGeNET

The Human Phenotype Ontology

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HPO ID	HPO Term
HP:0000006	Autosomal dominant inheritance
HP:0000007	Autosomal recessive inheritance
HP:0000028	Cryptorchidism
HP:0000035	Abnormal testis morphology
HP:0000054	Micropenis
HP:0000083	Renal insufficiency
HP:0000135	Hypogonadism
HP:0000252	Microcephaly
HP:0000348	High forehead
HP:0000405	Conductive hearing impairment

Displaying **all 4** entries
Disease ID	Disease Name
OMIM:617836	developmental delay and seizures with or without movement abnormalities
ORPHA:442835	developmental and epileptic encephalopathy, 58 developmental delay and seizures with or without movement abnormalities intellectual disability, X-linked, syndromic, Houge type intellectual disability, autosomal dominant 55, with seizures intellectual disability, autosomal dominant 56 undetermined early-onset epileptic encephalopathy
ORPHA:791	Leber congenital amaurosis 14 Leber congenital amaurosis 4 retinitis pigmentosa
OMIM:613861	retinitis pigmentosa 59

PubChem Disease

MedGen Diseases

OMIM Phenotypes

KEGG Diseases

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

Ortholog

Displaying entries **71 - 80** of 88 in total

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Species	Gene ID	Orthologous MAtrix
Rhinopithecus bieti	108518187	RHIBE20584
Rhinopithecus roxellana	104675752	RHIRO09647
Nomascus leucogenys	100603801	NOMLE23123
Podarcis muralis	114601527	PODMU31526
Sinocyclocheilus grahami	107552517	SINGR74038
Chelonoidis abingdonii	116837973	CHEAB02452
Pteropus vampyrus	105290493	PTEVA14160
Echeneis naucrates	115045189	ECHNA26687
Salarias fasciatus	115397132	SALFA31786
Athene cunicularia	113488396	ATHCN21707

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

Summary

External Links

Annotation

KEGG BRITE Database

PubChem Disease

International Collaboration

Acknowledgements