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          • › C_338807846_10
          See other PRMT7 GT Assays ›
          SNP ID:
          rs757033150
          Gene
          PRMT7 SLC7A6OS
          Gene Name
          protein arginine methyltransferase 7
          solute carrier family 7 member 6 opposite strand
          Set Membership:
          -
          Chromosome Location:
          Chr.16: 68311884 - 68311884 on Build GRCh38
          Polymorphism:
          T/G, Transversion substitution
          Context Sequence [VIC/FAM]:

          ACAACGCTCTGTGTATTTCTTGCAT[T/G]CATGTAGTCTGTAATTTGTATTACT

          Assay ID C_338807846_10
          Size
          Availability Made To Order
          Catalog # 4351379
          Price
          Your Price
          Online offer:
          Check your price ›
          • Genomic Map
          • Assay Details
          • More Information

          Genomic Map

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          Assay Details



          Species:

          Human

          dbSNP Submissions:

          NA

          Phenotype:

          MIM: 610087

          Literature Links:

          PRMT7 PubMed Links

          Allele Nomenclature:

          Minor Allele Frequency:

          1000Genome Applied Biosystems® HapMap
          Global - Not Available Caucasian - Not Available CEPH (CEU) - Not Available
          EAS - Not Available African American - Not Available YRI (Yoruba) - Not Available
          SAS - Not Available Chinese - Not Available CHB (Han Chinese) - Not Available
          AFR - Not Available Japanese - Not Available JPT (Japanese) - Not Available
          EUR - Not Available
          AMR - Not Available
          PRMT7 - protein arginine methyltransferase 7
          Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
          NM_001184824.1 Intron NP_001171753.1
          NM_001290018.1 Intron NP_001276947.1
          NM_019023.2 Intron NP_061896.1
          XM_011523112.2 Intron XP_011521414.1
          XM_011523113.2 Intron XP_011521415.1
          XM_011523115.2 Intron XP_011521417.1
          XM_011523116.2 Intron XP_011521418.1
          XM_011523121.2 Intron XP_011521423.1
          XM_011523124.2 Intron XP_011521426.1
          XM_011523125.2 Intron XP_011521427.1
          XM_011523126.2 Intron XP_011521428.1
          XM_011523128.2 Intron XP_011521430.1
          XM_011523131.2 Intron XP_011521433.1
          XM_017023290.1 Intron XP_016878779.1
          XM_017023291.1 Intron XP_016878780.1
          XM_017023292.1 Intron XP_016878781.1
          XM_017023293.1 Intron XP_016878782.1
          XM_017023294.1 Intron XP_016878783.1
          XM_017023295.1 Intron XP_016878784.1
          XM_017023296.1 Intron XP_016878785.1
          XM_017023297.1 Intron XP_016878786.1
          XM_017023298.1 Intron XP_016878787.1
          XM_017023299.1 Intron XP_016878788.1
          XM_017023300.1 Intron XP_016878789.1
          XM_017023301.1 Intron XP_016878790.1
          XM_017023302.1 Intron XP_016878791.1
          XM_017023303.1 Intron XP_016878792.1
          XM_017023304.1 Intron XP_016878793.1
          XM_017023305.1 Intron XP_016878794.1
          XM_017023306.1 Intron XP_016878795.1
          XM_017023307.1 Intron XP_016878796.1
          XM_017023308.1 Intron XP_016878797.1
          XM_017023309.1 Intron XP_016878798.1
          XM_017023310.1 Intron XP_016878799.1
          XM_017023311.1 Intron XP_016878800.1
          XM_017023312.1 Intron XP_016878801.1
          XM_017023313.1 Intron XP_016878802.1
          XM_017023314.1 Intron XP_016878803.1
          XM_017023315.1 Intron XP_016878804.1
          XM_017023316.1 Intron XP_016878805.1
          SLC7A6OS - solute carrier family 7 member 6 opposite strand
          Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
          NM_032178.2 Intron NP_115554.2
          XM_011523372.2 Intron XP_011521674.1

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          More Information


          Panther Classification:

          Molecular Function -

          protein modifying enzyme

          Gene Ontology Categories:

          Function(s) Process(es)

          spliceosomal snRNP assembly
          regulation of gene expression by genetic imprinting
          transcription, DNA-templated
          regulation of transcription, DNA-templated
          histone methylation
          peptidyl-arginine methylation
          peptidyl-arginine methylation, to symmetrical-dimethyl arginine
          peptidyl-arginine methylation, to asymmetrical-dimethyl arginine
          cell differentiation
          histone arginine methylation
          DNA methylation involved in gamete generation
          regulation of protein binding
          histone H4-R3 methylation
          hematopoietic progenitor cell differentiation
          protein transport
          histone-arginine N-methyltransferase activity
          S-adenosylmethionine-dependent methyltransferase activity
          protein-arginine N-methyltransferase activity
          [myelin basic protein]-arginine N-methyltransferase activity
          protein-arginine omega-N monomethyltransferase activity
          protein-arginine omega-N asymmetric methyltransferase activity
          protein-arginine omega-N symmetric methyltransferase activity
          histone binding
          ribonucleoprotein complex binding
          histone methyltransferase activity (H4-R3 specific)

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