Entity Details

Primary name LIN41_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ2Q1W2
EntryNameLIN41_HUMAN
FullNameE3 ubiquitin-protein ligase TRIM71
TaxID9606
Evidenceevidence at protein level
Length868
SequenceStatuscomplete
DateCreated2007-03-06
DateModified2021-06-02

Ontological Relatives

GenesTRIM71

GO terms

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GOName
GO:0000082 G1/S transition of mitotic cell cycle
GO:0000209 protein polyubiquitination
GO:0000932 P-body
GO:0001843 neural tube closure
GO:0004842 ubiquitin-protein transferase activity
GO:0008270 zinc ion binding
GO:0008543 fibroblast growth factor receptor signaling pathway
GO:0010586 miRNA metabolic process
GO:0010608 posttranscriptional regulation of gene expression
GO:0017148 negative regulation of translation
GO:0021915 neural tube development
GO:0030371 translation repressor activity
GO:0035196 production of miRNAs involved in gene silencing by miRNA
GO:0035198 miRNA binding
GO:0035278 miRNA mediated inhibition of translation
GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process
GO:0051865 protein autoubiquitination
GO:0060964 regulation of gene silencing by miRNA
GO:0061158 3'-UTR-mediated mRNA destabilization
GO:0061630 ubiquitin protein ligase activity
GO:0072089 stem cell proliferation
GO:2000177 regulation of neural precursor cell proliferation
GO:2000637 positive regulation of gene silencing by miRNA

Subcellular Location

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Subcellular Location
Cytoplasm

Domains

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DomainNameCategoryType
IPR000315 B-box-type zinc fingerDomainDomain
IPR001258 NHL repeatRepeatRepeat
IPR001298 Filamin/ABP280 repeatRepeatRepeat
IPR001841 Zinc finger, RING-typeDomainDomain
IPR011042 Six-bladed beta-propeller, TolB-likeFamilyHomologous superfamily
IPR013017 NHL repeat, subgroupRepeatRepeat
IPR013083 Zinc finger, RING/FYVE/PHD-typeFamilyHomologous superfamily
IPR013783 Immunoglobulin-like foldFamilyHomologous superfamily
IPR014756 Immunoglobulin E-setFamilyHomologous superfamily
IPR017868 Filamin/ABP280 repeat-likeRepeatRepeat
IPR017907 Zinc finger, RING-type, conserved siteSiteConserved site

Diseases

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Disease IDSourceNameDescription
618667 OMIMHydrocephalus, congenital communicating, 1 (HYDCC1)A form of congenital hydrocephalus, a disease characterized by onset in utero of enlarged ventricles due to accumulation of ventricular cerebrospinal fluid. Affected individuals may have neurologic impairment. HYDCC1 inheritance is autosomal dominant. The disease is caused by variants affecting the gene represented in this entry.