Version: 8.0.0
Date: Tue Jan 28 2025
1,995 results for prmt9

Prmt9

(Mus musculus)
Gene
Name: protein arginine methyltransferase 9
Synonyms: expressed sequence AI931714, Prmt10, AI931714, RGD1306157, protein arginine methyltransferase 10 (putative)
Source: MGI:2142651
Biotype: protein coding gene
Symbol: Prmt9 (Mmu)
Symbol: Prmt9
Automated Gene Synopsis: Orthologous to human PRMT9 (protein arginine methyltransferase 9).
Strict Orthology Symbols: prmt9
Alleles: Prmt9 (Mmu)...Prmt9 (Mmu)

Prmt9

(Rattus norvegicus)
Gene
Name: protein arginine methyltransferase 9
Synonyms: putative protein arginine N-methyltransferase 9, similar to CG9882-PA, putative protein arginine N-methyltransferase 10, Prmt10, LOC291947, RGD1306157, protein arginine methyltransferase 10 (putative)
Source: RGD:1306157
Biotype: protein coding gene
Symbol: Prmt9 (Rno)
Symbol: Prmt9
Gene Synopsis: Orthologous to human PRMT9 (protein arginine methyltransferase 9); INTERACTS WITH bisphenol A; 2-hydroxypropanoic
Automated Gene Synopsis: Orthologous to human PRMT9 (protein arginine methyltransferase 9).
Strict Orthology Symbols: prmt9

prmt9

(Danio rerio)
Gene
Name: protein arginine methyltransferase 9
Synonyms: prmt10, zgc:195220
Source: ZFIN:ZDB-GENE-080728-4
Biotype: protein coding gene
Symbol: prmt9 (Dre)
Symbol: prmt9
Automated Gene Synopsis: Orthologous to human PRMT9 (protein arginine methyltransferase 9).
Strict Orthology Symbols: prmt9

PRMT9

(Homo sapiens)
Gene
Name: protein arginine methyltransferase 9
Synonyms: putative protein arginine N-methyltransferase 9, PRMT10, putative protein arginine N-methyltransferase 10, FLJ46629, protein arginine methyltransferase 10 (putative)
Source: HGNC:25099
Biotype: protein coding gene
Symbol: PRMT9 (Hsa)
Symbol: PRMT9
Strict Orthology Symbols: prmt9

prmt9

(Xenopus tropicalis)
Gene
Name: protein arginine methyltransferase 9
Synonyms: protein arginine methyltransferase 9, prmt9
Source: Xenbase:XB-GENE-5998444
Biotype: gene
Symbol: prmt9
Symbol: prmt9 (Xtr)
Automated Gene Synopsis: Orthologous to human PRMT9 (protein arginine methyltransferase 9).
Synonyms: prmt9...prmt9...prmt9
Strict Orthology Symbols: prmt9

prmt9.L

(Xenopus laevis)
Gene
Name: protein arginine methyltransferase 9
Synonyms: prmt9.L, protein arginine methyltransferase 9
Source: Xenbase:XB-GENE-5998467
Biotype: gene
Symbol: prmt9.L (Xla)
Automated Gene Synopsis: Orthologous to human PRMT9 (protein arginine methyltransferase 9).
Strict Orthology Symbols: prmt9
Symbol: prmt9.L

Prmt9em1Cya

(Mus musculus)
Allele/Variant
Source: MGI:7336180
Genes: Prmt9 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Prmt9 (Mmu)
Genes: Prmt9 (Mmu)
Symbol: Prmt9em1Cya

Prmt9em1(IMPC)J

(Mus musculus)
Allele/Variant
Source: MGI:6104244
Genes: Prmt9 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Prmt9 (Mmu)
Genes: Prmt9 (Mmu)
Symbol: Prmt9em1(IMPC)J

Prmt9em1(IMPC)J/Prmt9em1(IMPC)J [background:] C57BL/6NJ-Prmt9em1(IMPC)J/Mmjax

(Mus musculus)
Model
Id: MGI:6288676
Synonyms: Not Available
Symbol: Prmt9/Prmt9 [background:] C57BL/6NJ-Prmt9/Mmjax (Mmu)
Genes: Prmt9 (Mmu)
Alleles: Prmt9 (Mmu)
Name: Prmt9/Prmt9 [background:] C57BL/6NJ-Prmt9/Mmjax

Prmt9em1Cya/Prmt9em1Cya Lyz2tm1(cre)Ifo/Lyz2+ [background:] involves: 129P2/OlaHsd * C57BL/6N

(Mus musculus)
Model
Id: MGI:7336222
Synonyms: Not Available
Symbol: Prmt9/Prmt9 Lyz2/Lyz2<+> [background:] involves: 129P2/OlaHsd * C57BL/6N
Genes: Prmt9 (Mmu)
Alleles: Prmt9 (Mmu)
Name: Prmt9/Prmt9 Lyz2/Lyz2<+> [background:] involves: 129P2/OlaHsd * C57BL/6N

prmt-9

(Caenorhabditis elegans)
Gene
Name: PRotein arginine MethylTransferase 9
Synonyms: T23B5.1, prmt-3, CELE_T23B5.1
Source: WB:WBGene00011939
Biotype: protein coding gene
Gene Synopsis: Is an ortholog of human PRMT9 (protein arginine methyltransferase 9).
Automated Gene Synopsis: Orthologous to human PRMT9 (protein arginine methyltransferase 9).
Strict Orthology Symbols: prmt9

FBXO11

(Homo sapiens)
Gene
Name: F-box protein 11
Synonyms: vitiligo-associated protein 1, F-box protein Fbx11, FBX11, vitiligo-associated protein VIT-1, ubiquitin protein ligase E3 component n-recognin 6, FLJ12673, IDDFBA, F-box only protein 11, UG063H01, protein arginine N-methyltransferase 9, UBR6, VIT1, MGC44383, PRMT9
Source: HGNC:13590
Biotype: protein coding gene
Synonyms: PRMT9...PRMT9

protein-arginine omega-N symmetric methyltransferase activity

Gene Ontology
Source: GO:0035243
Synonyms:
  • S-adenosyl-L-methionine:[protein]-L-arginine N-methyltransferase ([protein]-Nomega,Nomega'-dimethyl-L-arginine-forming)
  • protein arginine omega-N symmetric methylase activity
Branch: molecular function
Genes: PRMT9 (Hsa)...Prmt9 (Mmu)...Prmt9 (Rno)

histone arginine N-methyltransferase activity

Gene Ontology
Source: GO:0008469
Synonyms:
  • S-adenosyl-L-methionine:histone-arginine nomega-methyltransferase activity
  • S-adenosyl-L-methionine:histone-arginine omega-N-methyltransferase activity
Branch: molecular function
Genes: PRMT9 (Hsa)...Prmt9 (Mmu)

protein-arginine N-methyltransferase activity

Gene Ontology
Source: GO:0016274
Synonyms:
  • PRMT activity
Branch: molecular function
Genes: Prmt9 (Rno)...PRMT9 (Hsa)...Prmt9 (Mmu)...prmt9 (Dre)

zko678a

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-171115-489
Genes: prmt9 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: prmt9 (Dre)

histone H4K12 methyltransferase activity

Gene Ontology
Source: GO:0140984
Synonyms:
  • histone H4 lysine 12-specific methyltransferase activity
  • histone H4K12 methylase activity
Branch: molecular function
Genes: PRMT9 (Hsa)...Prmt9 (Mmu)

histone H3R17 methyltransferase activity

Gene Ontology
Source: GO:0035642
Synonyms:
  • histone methylase activity (H3-R17 specific)
  • histone methyltransferase activity (H3-R17 specific)
Branch: molecular function
Genes: PRMT9 (Hsa)...Prmt9 (Mmu)

histone H3R8 methyltransferase activity

Gene Ontology
Source: GO:0140592
Synonyms:
  • histone H3R8 arginine methylase activity
  • histone H3R8 arginine methyltransferase activity
Branch: molecular function
Genes: PRMT9 (Hsa)...Prmt9 (Mmu)

histone H3K37 methyltransferase activity

Gene Ontology
Source: GO:0062122
Synonyms:
  • histone H3K37 methylase activity
  • histone lysine N-methyltransferase activity (H3-K37 specific)
Branch: molecular function
Genes: PRMT9 (Hsa)...Prmt9 (Mmu)

histone H3R26 methyltransferase activity

Gene Ontology
Source: GO:0140903
Synonyms:
  • histone H3R26 arginine methyltransferase activity
  • histone methylase activity (H3-R26 specific)
Branch: molecular function
Genes: PRMT9 (Hsa)...Prmt9 (Mmu)

histone H3R2 methyltransferase activity

Gene Ontology
Source: GO:0070611
Synonyms:
  • histone H3R2 arginine methyltransferase activity
  • histone methylase activity (H3-R2 specific)
Branch: molecular function
Genes: PRMT9 (Hsa)...Prmt9 (Mmu)

histone H2AQ104 methyltransferase activity

Gene Ontology
Source: GO:1990259
Synonyms:
  • histone glutamine N-methyltransferase activity
  • histone glutamine methylase activity
Branch: molecular function
Genes: PRMT9 (Hsa)...Prmt9 (Mmu)

histone H4R3 methyltransferase activity

Gene Ontology
Source: GO:0044020
Synonyms:
  • histone H4KR3 methylation
  • histone H4R3 arginine methylase activity
Branch: molecular function
Genes: PRMT9 (Hsa)...Prmt9 (Mmu)

histone H3K56 methyltransferase activity

Gene Ontology
Source: GO:0140759
Synonyms:
  • histone H3K56 methylase activity
  • histone lysine N-methyltransferase activity (H3-K56 specific)
Branch: molecular function
Genes: PRMT9 (Hsa)...Prmt9 (Mmu)

histone methyltransferase activity

Gene Ontology
Source: GO:0042054
Synonyms:
  • histone N-methyltransferase activity
  • histone methylase activity
Branch: molecular function
Genes: PRMT9 (Hsa)...Prmt9 (Rno)...Prmt9 (Mmu)...prmt9 (Dre)

peptidyl-arginine methylation

Gene Ontology
Source: GO:0018216
Synonyms: Not Available
Branch: biological process
Genes: prmt9 (Dre)

methylation

Gene Ontology
Source: GO:0032259
Synonyms: Not Available
Branch: biological process
Genes: PRMT9 (Hsa)...Prmt9 (Rno)...Prmt9 (Mmu)...prmt9 (Dre)

methyltransferase activity

Gene Ontology
Source: GO:0008168
Synonyms:
  • methylase
Branch: molecular function
Genes: PRMT9 (Hsa)...prmt9 (Dre)

mRNA processing

Gene Ontology
Source: GO:0006397
Synonyms:
  • mRNA maturation
Branch: biological process
Genes: PRMT9 (Hsa)...Prmt9 (Rno)...Prmt9 (Mmu)

regulation of DNA-templated transcription

Gene Ontology
Source: GO:0006355
Synonyms:
  • regulation of cellular transcription, DNA-dependent
  • regulation of gene-specific transcription
Branch: biological process
Genes: PRMT9 (Hsa)...Prmt9 (Mmu)...Prmt9 (Rno)...prmt9 (Dre)

chromatin remodeling

Gene Ontology
Source: GO:0006338
Synonyms:
  • ATP-dependent chromatin remodeling
  • ATP-dependent chromatin remodelling
Branch: biological process
Genes: PRMT9 (Hsa)...Prmt9 (Mmu)...Prmt9 (Rno)...prmt9 (Dre)

sa32715

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-1872
Genes: prmt9 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: prmt9 (Dre)

sa13445

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-130411-3065
Genes: prmt9 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: prmt9 (Dre)

transferase activity

Gene Ontology
Source: GO:0016740
Synonyms: Not Available
Branch: molecular function
Genes: prmt9 (Dre)

sa13342

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-130411-2977
Genes: prmt9 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: prmt9 (Dre)

sa14984

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-130411-3603
Genes: prmt9 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: prmt9 (Dre)

(GRCh38)2:47808188G>C

(Homo sapiens)
Allele/Variant
Source: rs1670356255
Genes: MSH6 (Hsa), FBXO11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:47808188G>C
Gene Synonyms: PRMT9

(GRCh38)2:47808229A>G

(Homo sapiens)
Allele/Variant
Source: rs903240623
Genes: MSH6 (Hsa), FBXO11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:47808229A>G
Gene Synonyms: PRMT9

(GRCh38)2:47808184T>G

(Homo sapiens)
Allele/Variant
Source: rs533101051
Genes: MSH6 (Hsa), FBXO11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:47808184T>G
Gene Synonyms: PRMT9

(GRCh38)2:47809682A>T

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.47809682A>T
Genes: MSH6 (Hsa), FBXO11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:47809682A>T
Gene Synonyms: PRMT9

(GRCh38)2:47808355A>G

(Homo sapiens)
Allele/Variant
Source: rs1026600064
Genes: MSH6 (Hsa), FBXO11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:47808355A>G
Gene Synonyms: PRMT9

(GRCh38)2:47809688G>A

(Homo sapiens)
Allele/Variant
Source: rs757286262
Genes: MSH6 (Hsa), FBXO11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:47809688G>A
Gene Synonyms: PRMT9

(GRCh38)2:47808155G>A

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.47808155G>A
Genes: MSH6 (Hsa), FBXO11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:47808155G>A
Gene Synonyms: PRMT9

(GRCh38)2:47809153G>A

(Homo sapiens)
Allele/Variant
Source: rs368811481
Genes: MSH6 (Hsa), FBXO11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:47809153G>A
Gene Synonyms: PRMT9

(GRCh38)2:47809239G>C

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.47809239G>C
Genes: MSH6 (Hsa), FBXO11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:47809239G>C
Gene Synonyms: PRMT9

(GRCh38)2:47808393T>A

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.47808393T>A
Genes: MSH6 (Hsa), FBXO11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:47808393T>A
Gene Synonyms: PRMT9

(GRCh38)2:47808121G>A

(Homo sapiens)
Allele/Variant
Source: rs756515981
Genes: MSH6 (Hsa), FBXO11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:47808121G>A
Gene Synonyms: PRMT9

(GRCh38)2:47809646C>T

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.47809646C>T
Genes: MSH6 (Hsa), FBXO11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:47809646C>T
Gene Synonyms: PRMT9

(GRCh38)2:47808364A>G

(Homo sapiens)
Allele/Variant
Source: rs1670371300
Genes: MSH6 (Hsa), FBXO11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:47808364A>G
Gene Synonyms: PRMT9