Version: 8.1.0Date: Fri Apr 18 2025
Category
alg-4
(Caenorhabditis elegans)Gene
Name: Argonaute (plant)-Like Gene 4
Synonyms: ZK757.3, CELE_ZK757.3, tag-76
Source: WB:WBGene00006449
Biotype: protein coding gene
Symbol: alg-4 (Cel)
Symbol: alg-4
Gene Synopsis: alg-4 encodes an Argonaute (AGO) protein that is a member of the AGO clade of Argonaute small RNA-binding...proteins; together with its paralog, alg-3, alg-4 is required for normal brood sizes at elevated temperatures
Cross References: WB:alg-4...alg-4...alg-4
pdcd11
(Xenopus tropicalis)Gene
Name: programmed cell death 11
Synonyms: programmed cell death 11, rrp5, alg4, nfbp, alg-4, pdcd11
Source: Xenbase:XB-GENE-967218
Biotype: gene
Synonyms: alg-4...alg-4...alg-4...alg-4
pdcd11.L
(Xenopus laevis)Gene
Name: programmed cell death 11
Synonyms: programmed cell death 11, rrp5, alg4, nfbp, pdcd11.L, alg-4
Source: Xenbase:XB-GENE-967222
Biotype: gene
Synonyms: alg-4...alg-4...alg-4...alg-4
Pdcd11
(Mus musculus)Gene
Name: programmed cell death 11
Synonyms: 1110021I22Rik, RIKEN cDNA 1110021I22 gene, ALG-4, mKIAA0185
Source: MGI:1341788
Biotype: protein coding gene
Synonyms: ALG-4...ALG-4...ALG-4
PDCD11
(Homo sapiens)Gene
Name: programmed cell death 11
Synonyms: NFBP, RRP5, ALG-4, ALG4, KIAA0185, programmed cell death protein 11, apoptosis-linked gene 4, NF-kappa-B-binding protein, protein RRP5 homolog
Source: HGNC:13408
Biotype: protein coding gene
Synonyms: ALG-4...ALG-4...ALG-4
ok1041
(Caenorhabditis elegans)Allele/Variant
Source: WB:WBVar00092311
Genes: alg-4 (Cel)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: alg-4 (Cel)
RB1079
(Caenorhabditis elegans)Model
Id: WB:WBStrain00031783
Synonyms: Not Available
Genes: alg-4 (Cel)
Pdcd11Gt(VET36A)Hiir
(Mus musculus)Allele/Variant
Source: MGI:5696394
Genes: Pdcd11 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: ALG-4
Pdcd11em2Gpt
(Mus musculus)Allele/Variant
Source: MGI:7303993
Genes: Pdcd11 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: ALG-4
Pdcd11em1Gpt
(Mus musculus)Allele/Variant
Source: MGI:7377000
Genes: Pdcd11 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: ALG-4
Source: GO:0035194
Synonyms:
- PTGS
- RNA interference
Branch: biological process
Genes: alg-4 (Cel)
Gene Ontology
Source: GO:0035198
Synonyms:
- microRNA binding
Branch: molecular function
Genes: alg-4 (Cel)
Gene Ontology
Source: GO:0043186
Synonyms:
- germline granule
- nuage
Branch: cellular component
Genes: alg-4 (Cel)
Gene Ontology
Source: GO:0004521
Synonyms:
- endonuclease G activity
- endoribonuclease activity
Branch: molecular function
Genes: alg-4 (Cel)
Gene Ontology
Source: GO:0003727
Synonyms:
- ssRNA binding
Branch: molecular function
Genes: alg-4 (Cel)
Gene Ontology
Source: GO:0036464
Synonyms:
- Staufen granule
Branch: cellular component
Genes: alg-4 (Cel)
Gene Ontology
Source: GO:0016442
Synonyms:
- RNA-induced silencing complex
- miRNP complex
Branch: cellular component
Genes: alg-4 (Cel)
(GRCh38)10:103440806C>T
(Homo sapiens)Allele/Variant
Source: rs746440287
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103440806C>T
Gene Synonyms: ALG-4
(GRCh38)10:103434819G>A
(Homo sapiens)Allele/Variant
Source: NC_000010.11:g.103434819G>A
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103434819G>A
Gene Synonyms: ALG-4
(GRCh38)10:103440816A>G
(Homo sapiens)Allele/Variant
Source: rs749683033
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103440816A>G
Gene Synonyms: ALG-4
(GRCh38)10:103444027G>A
(Homo sapiens)Allele/Variant
Source: rs201517950
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103444027G>A
Gene Synonyms: ALG-4
(GRCh38)10:103442318G>A
(Homo sapiens)Allele/Variant
Source: rs763397616
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103442318G>A
Gene Synonyms: ALG-4
(GRCh38)10:103443999C>T
(Homo sapiens)Allele/Variant
Source: rs371182913
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103443999C>T
Gene Synonyms: ALG-4
(GRCh38)10:103423084G>A
(Homo sapiens)Allele/Variant
Source: rs778314230
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103423084G>A
Gene Synonyms: ALG-4
(GRCh38)10:103419698C>T
(Homo sapiens)Allele/Variant
Source: rs748169961
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103419698C>T
Gene Synonyms: ALG-4
(GRCh38)10:103424984C>G
(Homo sapiens)Allele/Variant
Source: NC_000010.11:g.103424984C>G
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103424984C>G
Gene Synonyms: ALG-4
(GRCh38)10:103425077T>C
(Homo sapiens)Allele/Variant
Source: rs199624392
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103425077T>C
Gene Synonyms: ALG-4
(GRCh38)10:103417840C>T
(Homo sapiens)Allele/Variant
Source: rs765544212
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103417840C>T
Gene Synonyms: ALG-4
(GRCh38)10:103409706C>T
(Homo sapiens)Allele/Variant
Source: rs267602350
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103409706C>T
Gene Synonyms: ALG-4
(GRCh38)10:103409718C>T
(Homo sapiens)Allele/Variant
Source: rs772637975
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103409718C>T
Gene Synonyms: ALG-4
(GRCh38)10:103434021C>G
(Homo sapiens)Allele/Variant
Source: NC_000010.11:g.103434021C>G
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103434021C>G
Gene Synonyms: ALG-4
(GRCh38)10:103440549G>T
(Homo sapiens)Allele/Variant
Source: rs761022665
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103440549G>T
Gene Synonyms: ALG-4
(GRCh38)10:103433957G>A
(Homo sapiens)Allele/Variant
Source: rs747568130
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103433957G>A
Gene Synonyms: ALG-4
(GRCh38)10:103406079C>T
(Homo sapiens)Allele/Variant
Source: NC_000010.11:g.103406079C>T
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103406079C>T
Gene Synonyms: ALG-4
(GRCh38)10:103406759C>T
(Homo sapiens)Allele/Variant
Source: NC_000010.11:g.103406759C>T
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103406759C>T
Gene Synonyms: ALG-4
(GRCh38)10:103413174G>A
(Homo sapiens)Allele/Variant
Source: rs548314013
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103413174G>A
Gene Synonyms: ALG-4
(GRCh38)10:103434939C>T
(Homo sapiens)Allele/Variant
Source: rs200115454
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103434939C>T
Gene Synonyms: ALG-4
(GRCh38)10:103421470G>A
(Homo sapiens)Allele/Variant
Source: rs752195699
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103421470G>A
Gene Synonyms: ALG-4
(GRCh38)10:103423024C>T
(Homo sapiens)Allele/Variant
Source: rs142052555
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103423024C>T
Gene Synonyms: ALG-4
(GRCh38)10:103433997G>A
(Homo sapiens)Allele/Variant
Source: rs61760969
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103433997G>A
Gene Synonyms: ALG-4
(GRCh38)10:103409747G>A
(Homo sapiens)Allele/Variant
Source: rs141352682
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103409747G>A
Gene Synonyms: ALG-4
(GRCh38)10:103423031G>A
(Homo sapiens)Allele/Variant
Source: rs377375510
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103423031G>A
Gene Synonyms: ALG-4
(GRCh38)10:103427370C>T
(Homo sapiens)Allele/Variant
Source: rs766219191
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103427370C>T
Gene Synonyms: ALG-4
(GRCh38)10:103406680A>T
(Homo sapiens)Allele/Variant
Source: NC_000010.11:g.103406680A>T
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103406680A>T
Gene Synonyms: ALG-4
(GRCh38)10:103409705C>T
(Homo sapiens)Allele/Variant
Source: rs267602349
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103409705C>T
Gene Synonyms: ALG-4
(GRCh38)10:103440354G>A
(Homo sapiens)Allele/Variant
Source: rs191321233
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103440354G>A
Gene Synonyms: ALG-4
(GRCh38)10:103443262G>A
(Homo sapiens)Allele/Variant
Source: NC_000010.11:g.103443262G>A
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103443262G>A
Gene Synonyms: ALG-4
(GRCh38)10:103418600G>A
(Homo sapiens)Allele/Variant
Source: rs769452865
Genes: PDCD11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:103418600G>A
Gene Synonyms: ALG-4