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          • › C_153104857_10
          See other LOC100287042 GT Assays ›
          SNP ID:
          rs113513403
          Gene
          LOC100287042 MIF4GD MRPS7 SLC25A19
          Gene Name
          uncharacterized LOC100287042
          MIF4G domain containing
          mitochondrial ribosomal protein S7
          solute carrier family 25 member 19
          Set Membership:
          -
          Chromosome Location:
          Chr.17: 75273496 - 75273496 on Build GRCh38
          Polymorphism:
          A/G, Transition substitution
          Context Sequence [VIC/FAM]:

          TGTTCATGCAGTGGAAGACATTACA[A/G]AAGAATTCATACGAGAAGAACATGA

          Assay ID C_153104857_10
          Size
          Availability Made To Order
          Catalog # 4351379
          Price
          Your Price
          Online offer:
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          • Genomic Map
          • Assay Details
          • More Information

          Genomic Map

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          Assay Details



          Species:

          Human

          dbSNP Submissions:

          NA

          Phenotype:

          MIM: 612072 MIM: 611974 MIM: 606521

          Literature Links:

          LOC100287042 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
          LOC100287042 - uncharacterized LOC100287042
          There are no transcripts associated with this gene.
          MIF4GD - MIF4G domain containing
          There are no transcripts associated with this gene.
          MRPS7 - mitochondrial ribosomal protein S7
          There are no transcripts associated with this gene.
          SLC25A19 - solute carrier family 25 member 19
          Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
          NM_001126121.1 1335 Silent Mutation TTC,TTT F,F 306 NP_001119593.1
          NM_001126122.1 1335 Silent Mutation TTC,TTT F,F 306 NP_001119594.1
          NM_021734.4 1335 Silent Mutation TTC,TTT F,F 306 NP_068380.3
          XM_005257559.3 1335 Silent Mutation TTC,TTT F,F 306 XP_005257616.1
          XM_005257560.2 1335 Silent Mutation TTC,TTT F,F 306 XP_005257617.1
          XM_005257561.3 1335 Silent Mutation TTC,TTT F,F 306 XP_005257618.1
          XM_005257562.2 1335 Silent Mutation TTC,TTT F,F 306 XP_005257619.1
          XM_006722007.2 1335 Silent Mutation TTC,TTT F,F 306 XP_006722070.1
          XM_011525098.1 1335 Silent Mutation TTC,TTT F,F 201 XP_011523400.1
          XM_017024926.1 1335 Silent Mutation TTC,TTT F,F 306 XP_016880415.1
          XM_017024927.1 1335 Silent Mutation TTC,TTT F,F 205 XP_016880416.1
          XM_017024928.1 1335 Silent Mutation TTC,TTT F,F 201 XP_016880417.1

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          More Information


          Panther Classification:

          Molecular Function -

          mitochondrial carrier protein

          Gene Ontology Categories:

          Function(s) Process(es)

          positive regulation of defense response to virus by host
          translation
          deoxynucleotide transport
          transmembrane transport
          xenophagy
          structural constituent of ribosome
          deoxynucleotide transmembrane transporter activity

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