Entity Details

Primary name ZN644_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9H582
EntryNameZN644_HUMAN
FullNameZinc finger protein 644
TaxID9606
Evidenceevidence at protein level
Length1327
SequenceStatuscomplete
DateCreated2004-12-07
DateModified2021-06-02

Ontological Relatives

GenesZNF644

GO terms

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GOName
GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding
GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific
GO:0005634 nucleus
GO:0006357 regulation of transcription by RNA polymerase II
GO:0046872 metal ion binding

Subcellular Location

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Subcellular Location
Nucleus

Domains

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DomainNameCategoryType
IPR013087 Zinc finger C2H2-typeDomainDomain
IPR036236 Zinc finger C2H2 superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
614167 OMIMMyopia 21, autosomal dominant (MYP21)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

1 interaction

InteractorPartnerSourcesPublicationsLink
ZN644_HUMANCDYL_HUMANBioGRID, IntAct19061646 26496610 details