Entity Details

Primary name ZC3HE_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ6PJT7
EntryNameZC3HE_HUMAN
FullNameZinc finger CCCH domain-containing protein 14
TaxID9606
Evidenceevidence at protein level
Length736
SequenceStatuscomplete
DateCreated2008-04-29
DateModified2021-06-02

Ontological Relatives

GenesZC3H14

GO terms

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GOName
GO:0003723 RNA binding
GO:0005634 nucleus
GO:0005730 nucleolus
GO:0005737 cytoplasm
GO:0008143 poly(A) binding
GO:0016607 nuclear speck
GO:0032839 dendrite cytoplasm
GO:0043488 regulation of mRNA stability
GO:0046872 metal ion binding
GO:1900364 negative regulation of mRNA polyadenylation
GO:1904115 axon cytoplasm
GO:1990904 ribonucleoprotein complex

Subcellular Location

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Subcellular Location
Cytoplasm
Nucleus speckle

Domains

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DomainNameCategoryType
IPR000571 Zinc finger, CCCH-typeDomainDomain
IPR040366 Nuclear polyadenylated RNA-binding protein Nab2/ZC3H14FamilyFamily

Diseases

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Disease IDSourceNameDescription
617125 OMIMMental retardation, autosomal recessive 56 (MRT56)A form of mental retardation, a disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. The disease is caused by variants affecting the gene represented in this entry.