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 **11 - 20** of **186** in total

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DO ID	Disease Name	Source
DOID:0060192	Crohn's colitis	DisGeNET
DOID:0060235	carnitine palmitoyltransferase II deficiency	DisGeNET
DOID:0060254	Robinow syndrome	DisGeNET
DOID:0060255	rippling muscle disease 2	DisGeNET
DOID:0060578	Noonan syndrome 1	DisGeNET
DOID:0060580	Noonan syndrome 2	DisGeNET
DOID:0060581	Noonan syndrome 3	DisGeNET
DOID:0060582	Noonan syndrome 4	DisGeNET
DOID:0060583	Noonan syndrome 5	DisGeNET
DOID:0060584	Noonan syndrome 6	DisGeNET

The Human Phenotype Ontology

Displaying entries **1 - 10** of 95 in total

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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 **41 - 50** of 88 in total

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Species	Gene ID	Alliance of Genome Resources	Orthologous MAtrix
Loxodonta africana	100675778		LOXAF09035
Sus scrofa	100524683		PIGXX29369
Bos taurus	523264		BOVIN25121
Capra hircus	102169144		CAPHI20007
Ovis aries	101110654		SHEEP09972
Dipodomys ordii	106000289		DIPOR06020
Cricetulus griseus	100767025		CRIGR19685
Mus musculus	67422	MGI:1914672	MOUSE40641
Rattus norvegicus	298541	RGD:1311560	RATNO32559
Cavia porcellus	100729457		CAVPO11900

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

Summary

External Links

Annotation

KEGG BRITE Database

PubChem Disease

International Collaboration

Acknowledgements