Entity Details

Primary name ER6L2_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ5T890
EntryNameER6L2_HUMAN
FullNameDNA excision repair protein ERCC-6-like 2
TaxID9606
Evidenceevidence at protein level
Length1561
SequenceStatuscomplete
DateCreated2008-03-18
DateModified2021-06-02

Ontological Relatives

GenesERCC6L2

GO terms

Show/Hide Table
GOName
GO:0003677 DNA binding
GO:0004386 helicase activity
GO:0005524 ATP binding
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0005739 mitochondrion
GO:0005815 microtubule organizing center
GO:0016787 hydrolase activity
GO:0019901 protein kinase binding
GO:0032991 protein-containing complex
GO:0034614 cellular response to reactive oxygen species
GO:0036297 interstrand cross-link repair
GO:0070615 nucleosome-dependent ATPase activity

Subcellular Location

Show/Hide Table
Subcellular Location
Cytoplasm
Mitochondrion
Nucleus

Domains

Show/Hide Table
DomainNameCategoryType
IPR000330 SNF2, N-terminalDomainDomain
IPR001650 Helicase, C-terminalDomainDomain
IPR002464 DNA/RNA helicase, ATP-dependent, DEAH-box type, conserved siteSiteConserved site
IPR002999 Tudor domainDomainDomain
IPR014001 Helicase superfamily 1/2, ATP-binding domainDomainDomain
IPR027417 P-loop containing nucleoside triphosphate hydrolaseFamilyHomologous superfamily
IPR029256 Helicase-associated putative binding domainDomainDomain
IPR038718 SNF2-like, N-terminal domain superfamilyFamilyHomologous superfamily

Diseases

Show/Hide Table
Disease IDSourceNameDescription
615715 OMIMBone marrow failure syndrome 2 (BMFS2)An autosomal recessive disorder characterized by trilineage bone marrow failure, bone marrow hypocellularity, learning difficulties, and microcephaly. Insufficient hematopoiesis results in peripheral blood cytopenias, affecting myeloid, erythroid and megakaryocyte lines. Cutaneous features and increased chromosome breakage are not features. The disease is caused by variants affecting the gene represented in this entry.

Interactions

3 interactions

InteractorPartnerSourcesPublicationsLink
ER6L2_HUMANCYREN_HUMANBioGRID, IntAct25416956 32296183 details
ER6L2_HUMANT11L1_HUMANBioGRID, IntAct32296183 details
ER6L2_HUMANNEK6_HUMANBioGRID20873783 details