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          • Home
          • › Search Tool
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          • › Hs01716960_cn
          See other FAM149A CNV Assays ›
          Gene Symbol
          FAM149A
          Assay Reference Genome
          Location

          Chr.4:186149618 on build GRCh38
          Cytoband
          Assay ID Hs01716960_cn
          Size
          Availability Made To Order
          Catalog # 4400291
          Price
          Your Price
          Online offer:
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          • Genomic Map
          • Assay Details
          • More Information

          Genomic Map

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          Assay Details

          Target Gene Details

          Entrez Gene ID:

          25854

          Gene Name:

          family with sequence similarity 149 member A

          Gene Aliases:

          MST119, MSTP119

          Location:

          Chr.4:186104704-186175337 on Build GRCh38

          Assay Gene Location:

          Overlaps Intron 4 - Exon 5
          Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
          FAM149A NM_001006655.3 NP_001006656.1
          NM_001350178.1 NP_001337107.1
          NM_001350179.1 NP_001337108.1
          NM_001367768.3 NP_001354697.1
          NM_001395294.1 NP_001382223.1
          NM_015398.4 NP_056213.1
          AF173894.1 AAQ13641.1
          AK057166.1 BAG51873.1
          AK295340.1 BAG58311.1
          AK297679.1 BAH12648.1
          AK309233.1
          AK311462.1
          BC110816.1 AAI10817.1
          BC142992.1 AAI42993.1
          BQ884007.1
          DA159632.1

          Target Copy Number Variation Details

          DGV Version:

          Release date: 2025-12-01, GRCh GRCh38
          Target
          Variation
          Location CNV
          Subtype
          Genes
          esv3894090 Chr.4:186011626 - 186212421 on Build GRCh38 Gain FAM149A KLKB1 TLR3 CYP4V2 FLJ38576
          nsv1016120 Chr.4:186125183 - 186169324 on Build GRCh38 Gain FAM149A
          nsv1028146 Chr.4:185582745 - 186417181 on Build GRCh38 Gain FAM149A KLKB1 F11-AS1 SORBS2-AS1 TLR3 CYP4V2 F11 SORBS2 FLJ38576
          nsv508340 Chr.4:186138019 - 186215804 on Build GRCh38 Deletion FAM149A KLKB1 CYP4V2 FLJ38576
          nsv6140977 Chr.4:186008703 - 186213068 on Build GRCh38 Duplication FAM149A KLKB1 TLR3 CYP4V2 FLJ38576
          nsv470097 Chr.4:186010756 - 186210350 on Build GRCh38 Gain FAM149A TLR3 CYP4V2 FLJ38576
          nsv4117959 Chr.4:185482576 - 186997201 on Build GRCh38 Deletion FAM149A KLKB1 F11-AS1 SORBS2-AS1 TLR3 PDLIM3 CYP4V2 FAT1 F11 SORBS2 MTNR1A FLJ38576
          nsv596400 Chr.4:186145486 - 186171321 on Build GRCh38 Loss FAM149A
          nsv4132364 Chr.4:186040783 - 186195278 on Build GRCh38 Deletion FAM149A TLR3 CYP4V2 FLJ38576
          nsv830172 Chr.4:186091611 - 186247270 on Build GRCh38 Loss FAM149A KLKB1 CYP4V2 FLJ38576
          dgv683n27 Chr.4:186008072 - 186210350 on Build GRCh38 Gain FAM149A TLR3 CYP4V2 FLJ38576
          nsv4521971 Chr.4:186115844 - 186466846 on Build GRCh38 Duplication FAM149A KLKB1 F11-AS1 CYP4V2 F11 FLJ38576
          nsv461864 Chr.4:186085652 - 186335850 on Build GRCh38 Gain FAM149A KLKB1 F11-AS1 TLR3 CYP4V2 F11 FLJ38576
          dgv1052e214 Chr.4:186072002 - 186212619 on Build GRCh38 Gain FAM149A KLKB1 TLR3 CYP4V2 FLJ38576

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          More Information


          Set Membership:

          Intragenic Non-exonic DGV Variation

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