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Pathways
Genes search result for Homo sapiens
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13 records found for search term Rnf6
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RGD IDSymbolNameDescriptionChrStartStopSpeciesAnnotationsMatchType
1314509RNF6ring finger protein 6The protein encoded by this gene contains a RING-H2 finger motif. Deletions and mutations in this gene were detected in esophageal squamous cell carcinoma (ESCC), suggesting that this protein may be a potential tumor suppressor. Studies of the mouse counterpart suggested a role of this protein in th132613211526223085Human135symbol , old_gene_name , COSMIC , Human Proteome Mapgene, protein-coding, REVIEWED [RefSeq]
5131388RNF6P1ring finger protein 6 pseudogene 1213937376339374421Humansymbol , COSMIC , Human Proteome Mapgene, pseudo, INFERRED [RefSeq]
1602493MID2midline 2The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to microtubular structures in the cytoplasm. Alternate splicing of this gX107825735107931637Human99old_gene_symbolgene, protein-coding, REVIEWED [RefSeq]
1347564MKRN1makorin ring finger protein 1This gene encodes a protein that belongs to a novel class of zinc finger proteins. The encoded protein functions as a transcriptional co-regulator, and as an E3 ubiquitin ligase that promotes the ubiquitination and proteasomal degradation of target proteins. The protein encoded by this gene is thoug7140453033140479569Human81old_gene_symbolgene, protein-coding, REVIEWED [RefSeq]
1321625MKRN2makorin ring finger protein 2This gene encodes a probable E3 ubiquitin ligase containing several zinc finger domains, that is a member of the makorin RING zinc-finger protein family. This gene overlaps the v-raf-1 murine leukemia viral oncogene homolog 1 (RAF1) gene in an antisense orientation and may have a co-regulatory funct31255708712583713Human88old_gene_symbolgene, protein-coding, REVIEWED [RefSeq]
1322529MKRN3makorin ring finger protein 3The protein encoded by this gene contains a RING (C3HC4) zinc finger motif and several C3H zinc finger motifs. This gene is intronless and imprinted, with expression only from the paternal allele. Disruption of the imprinting at this locus may contribute to Prader-Willi syndrome. An antisense RNA of152356567423568044Human171old_gene_symbolgene, protein-coding, REVIEWED [RefSeq]
1350230MKRN4Pmakorin ring finger protein 4, pseudogenePredicted to enable ubiquitin protein ligase activity. Predicted to be involved in protein ubiquitination. [provided by Alliance of Genome Resources, Jul 2025]X4083425440837807Human13old_gene_symbolgene, pseudo, INFERRED [RefSeq]
1349030MKRN9Pmakorin ring finger protein 9, pseudogeneINTERACTS WITH tebuconazole128778288587784711Human1old_gene_symbolgene, pseudo, VALIDATED [RefSeq]
733503MNAT1MNAT1 component of CDK activating kinaseThe protein encoded by this gene, along with cyclin H and CDK7, forms the CDK-activating kinase (CAK) enzymatic complex. This complex activates several cyclin-associated kinases and can also associate with TFIIH to activate transcription by RNA polymerase II. Two transcript variants encoding differe146073476160969965Human107old_gene_symbolgene, protein-coding, REVIEWED [RefSeq]
1315966NEURL1neuralized E3 ubiquitin protein ligase 1Predicted to enable translation factor activity, non-nucleic acid binding and ubiquitin protein ligase activity. Involved in negative regulation of Notch signaling pathway; negative regulation of cell population proliferation; and positive regulation of apoptotic process. Located in plasma membrane.10103493705103592546Human134old_gene_symbolgene, protein-coding, VALIDATED [RefSeq]
1349943PCGF1polycomb group ring finger 1PCGF1 is a mammalian homolog of the Drosophila polycomb group genes, which act as transcriptional repressors to regulate anterior-posterior patterning in early embryonic development (Nunes et al., 2001 [PubMed 11287196]). See also PCGF2 (MIM 600346).[supplied by OMIM, Aug 2008]27450504374507695Human89old_gene_symbolgene, protein-coding, VALIDATED [RefSeq]
1319563PEX10peroxisomal biogenesis factor 10This gene encodes a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in this gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger sy124039742413827Human339old_gene_symbolgene, protein-coding, REVIEWED [RefSeq]
2303667NEURL1Bneuralized E3 ubiquitin protein ligase 1BPredicted to enable ubiquitin protein ligase activity. Predicted to be involved in ubiquitin-dependent endocytosis. Located in actin cytoskeleton and cytosol. [provided by Alliance of Genome Resources, Jul 2025]5172641263172691540Human108old_gene_symbolgene, protein-coding, VALIDATED [RefSeq]