Entity Details

Primary name ZDHC9_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9Y397
EntryNameZDHC9_HUMAN
FullNamePalmitoyltransferase ZDHHC9
TaxID9606
Evidenceevidence at protein level
Length364
SequenceStatuscomplete
DateCreated2003-02-01
DateModified2021-06-02

Ontological Relatives

GenesZDHHC9

GO terms

Show/Hide Table
GOName
GO:0000139 Golgi membrane
GO:0000165 MAPK cascade
GO:0002178 palmitoyltransferase complex
GO:0005783 endoplasmic reticulum
GO:0005789 endoplasmic reticulum membrane
GO:0005794 Golgi apparatus
GO:0005829 cytosol
GO:0006612 protein targeting to membrane
GO:0016021 integral component of membrane
GO:0016409 palmitoyltransferase activity
GO:0018230 peptidyl-L-cysteine S-palmitoylation
GO:0018345 protein palmitoylation
GO:0019706 protein-cysteine S-palmitoyltransferase activity
GO:0031228 intrinsic component of Golgi membrane
GO:0043849 Ras palmitoyltransferase activity

Subcellular Location

Show/Hide Table
Subcellular Location
Endoplasmic reticulum membrane
Golgi apparatus membrane

Domains

Show/Hide Table
DomainNameCategoryType
IPR001594 Palmitoyltransferase, DHHC domainDomainDomain
IPR030292 Palmitoyltransferase ZDHHC9FamilyFamily

Diseases

Show/Hide Table
Disease IDSourceNameDescription
300799 OMIMIntellectual developmental disorder, X-linked, syndromic, Raymond type (MRXSR)A disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. Some MRXSR patients show additional features, including marfanoid habitus, epilepsy, facial dysmorphism, hypotonia, and behavioral problems. The disease is caused by variants affecting the gene represented in this entry.

Interactions

1 interaction

InteractorPartnerSourcesPublicationsLink
ZDHC9_HUMANCREB3_HUMANBioGRID, IntAct25910212 details