Entity Details

Primary name PRIPO_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ96LW4
EntryNamePRIPO_HUMAN
FullNameDNA-directed primase/polymerase protein
TaxID9606
Evidenceevidence at protein level
Length560
SequenceStatuscomplete
DateCreated2007-03-06
DateModified2021-06-02

Ontological Relatives

GenesPRIMPOL

GO terms

Show/Hide Table
GOName
GO:0003682 chromatin binding
GO:0003887 DNA-directed DNA polymerase activity
GO:0003896 DNA primase activity
GO:0005634 nucleus
GO:0005657 replication fork
GO:0005759 mitochondrial matrix
GO:0006264 mitochondrial DNA replication
GO:0008270 zinc ion binding
GO:0009411 response to UV
GO:0019985 translesion synthesis
GO:0030145 manganese ion binding
GO:0031297 replication fork processing
GO:0042276 error-prone translesion synthesis
GO:0043504 mitochondrial DNA repair
GO:0062176 R-loop disassembly

Subcellular Location

Show/Hide Table
Subcellular Location
Chromosome
Mitochondrion matrix
Nucleus

Domains

Show/Hide Table
DomainNameCategoryType
IPR002755 DNA primase, small subunitFamilyFamily

Diseases

Show/Hide Table
Disease IDSourceNameDescription
615420 OMIMMyopia 22, autosomal dominant (MYP22)A refractive error of the eye, in which parallel rays from a distant object come to focus in front of the retina, vision being better for near objects than for far. The disease is caused by variants affecting the gene represented in this entry.

Interactions

7 interactions