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

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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

Displaying entries **71 - 80** of 95 in total

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HPO ID	HPO Term
HP:0004305	Involuntary movements
HP:0004322	Short stature
HP:0005978	Type II diabetes mellitus
HP:0007018	Attention deficit hyperactivity disorder
HP:0007099	Chiari type I malformation
HP:0007663	Reduced visual acuity
HP:0007675	Progressive night blindness
HP:0007703	Abnormality of retinal pigmentation
HP:0007737	Bone spicule pigmentation of the retina
HP:0007787	Posterior subcapsular cataract

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

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Species	Gene ID	Alliance of Genome Resources	Orthologous MAtrix
Caenorhabditis elegans	266904	WB:WBGene00044025
Drosophila melanogaster	31708	FB:FBgn0029980
Callorhinchus milii	103179564		CALMI18186
Latimeria chalumnae	102361662		LATCH16991
Danio rerio	406468	ZFIN:ZDB-GENE-040426-2236	DANRE10769
Astyanax mexicanus	103040074		ASTMX17827
Ictalurus punctatus	108256361		ICTPU18517
Salmo salar	106605152		SALSA125978
Salmo trutta	115177113		SALTR84858
Salmo trutta	115177121		SALTR45329

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

Summary

External Links

Annotation

KEGG BRITE Database

PubChem Disease

International Collaboration

Acknowledgements