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See other SAMD11 CNV Assays ›
Gene Symbol
SAMD11
Assay Reference Genome
Location

Chr.1:940460 on build GRCh38
Cytoband
1p36.33
Assay ID Hs03353087_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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  • Genomic Map
  • Assay Details
  • More Information

Genomic Map

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Assay Details

Target Gene Details

Entrez Gene ID:

148398

Gene Name:

sterile alpha motif domain containing 11

Gene Aliases:

MRS

Location:

Chr.1:925741-944581 on Build GRCh38

Assay Gene Location:

Within Intron 7
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
SAMD11 NM_152486.2 NP_689699.2
AK054643.1 BAB70781.1
BC024295.2 AAH24295.1
BC033213.1 AAH33213.1
CN293867.1
JX093066.1
JX093067.1
JX093068.1
JX093069.1
JX093070.1
JX093071.1
JX093072.1
JX093073.1
JX093074.1
JX093075.1
JX093076.1
JX093077.1
JX093078.1
JX093079.1
JX093080.1
JX093081.1
JX093082.1
JX093083.1
JX093084.1
JX093085.1
JX093086.1
JX093087.1
JX093088.1
JX093089.1
JX093090.1
JX093091.1
JX093092.1
JX093093.1
JX093094.1
JX093095.1
JX093096.1
JX093097.1
JX093098.1
JX093099.1
JX093100.1
JX093101.1
JX093102.1
JX093103.1
JX093104.1
JX093105.1
JX093106.1
JX093107.1
JX093108.1
JX093109.1
JX093110.1

Target Copy Number Variation Details

DGV Version:

Release date: 2016-05-15, GRCh GRCh38
Target
Variation
Location CNV
Subtype
Genes
dgv15n54 Chr.1:934063 - 943937 on Build GRCh38 Loss SAMD11
esv2762302 Chr.1:914637 - 1106320 on Build GRCh38 Gain LOC100288175 AGRN SAMD11 LOC100130417 LOC105378948 KLHL17 RNF223 LOC107985728 ISG15 PERM1 LOC284600 PLEKHN1 HES4 NOC2L C1orf159
nsv482937 Chr.1:10001 - 2368561 on Build GRCh38 Loss LOC100288175 CALML6 UBE2J2 LOC105378947 ACAP3 LINC01128 PERM1 SLC35E2B CFAP74 SLC35E2 MIR200B B3GALT6 ATAD3C TNFRSF18 TMEM52 TTLL10-AS1 CCNL2 MIB2 LOC284600 AURKAIP1 PLEKHN1 OR4F29 WASH7P LOC105378949 TMEM240 MTND1P23 OR4F5 LOC100130417 TAS1R3 VWA1 SDF4 FAM138A LOC729737 DVL1 TTLL10 MIR6727 C1orf159 AGRN LOC100129534 DDX11L1 FAM132A LOC100133331 LOC107985728 ISG15 MIR200A GABRD LOC102724312 LOC100288069 HES4 LINC00115 MIR6726 CPSF3L LOC105378948 LOC105378592 LOC102725121 SKI LINC01342 NADK ATAD3A MIR6723 LOC107984841 MIR6859-2 NOC2L MMP23A LOC101928626 TMEM88B MXRA8 GNB1 PUSL1 KLHL17 MIR1302-2 MIR429 SCNN1D LOC100132287 LOC107985729 MORN1 CDK11B ATAD3B MTND2P28 SAMD11 PRKCZ LOC100134822 FAAP20 MIR6808 RNF223 LOC105378589 LOC100287934 CDK11A MRPL20 LOC148413 FAM41C LOC100506504 CPTP MMP23B MIR6859-1 FAM87B SSU72 ANKRD65 OR4F16 LOC105378591 FNDC10 TNFRSF4
nsv950451 Chr.1:899421 - 1094520 on Build GRCh38 Deletion LOC100288175 AGRN SAMD11 LOC100130417 LOC105378948 KLHL17 RNF223 LOC107985728 ISG15 PERM1 LOC284600 PLEKHN1 HES4 NOC2L C1orf159
nsv509035 Chr.1:891406 - 985724 on Build GRCh38 Insertion PERM1 LOC284600 SAMD11 PLEKHN1 LOC100130417 NOC2L KLHL17 LOC107985728
dgv9n54 Chr.1:925754 - 952840 on Build GRCh38 Loss SAMD11 NOC2L
nsv428334 Chr.1:874371 - 1220569 on Build GRCh38 Gain LOC100288175 SAMD11 LOC100130417 LOC105378948 SDF4 RNF223 LINC01342 PERM1 TTLL10 NOC2L MIR200B C1orf159 FAM41C AGRN TNFRSF18 KLHL17 TTLL10-AS1 LOC107985728 MIR429 ISG15 MIR200A LOC284600 PLEKHN1 HES4 TNFRSF4
nsv10161 Chr.1:776731 - 1777210 on Build GRCh38 Gain+Loss MIR6726 LOC100288175 UBE2J2 CPSF3L ACAP3 LOC105378948 LINC01128 LINC01342 NADK ATAD3A PERM1 SLC35E2B NOC2L SLC35E2 MIR200B B3GALT6 MMP23A TMEM88B MXRA8 ATAD3C TNFRSF18 PUSL1 KLHL17 TTLL10-AS1 CCNL2 MIR429 MIB2 LOC284600 AURKAIP1 SCNN1D PLEKHN1 LOC107985729 CDK11B TMEM240 ATAD3B SAMD11 LOC100130417 TAS1R3 VWA1 SDF4 MIR6808 RNF223 DVL1 TTLL10 LOC100287934 CDK11A MIR6727 MRPL20 LOC148413 C1orf159 FAM41C AGRN CPTP MMP23B FAM132A FAM87B SSU72 LOC107985728 ISG15 MIR200A ANKRD65 LOC102724312 LOC100288069 HES4 LINC00115 FNDC10 TNFRSF4
dgv5n100 Chr.1:585989 - 1114424 on Build GRCh38 Gain MTND1P23 LOC100288175 MTND2P28 SAMD11 LOC105378947 LOC100130417 LOC105378948 LINC01128 RNF223 MIR6723 PERM1 LOC107984841 LOC100287934 NOC2L C1orf159 FAM41C AGRN LOC101928626 FAM87B KLHL17 LOC100133331 LOC107985728 ISG15 LOC284600 OR4F16 LOC100288069 PLEKHN1 HES4 LINC00115
nsv517709 Chr.1:817186 - 1275912 on Build GRCh38 Gain+Loss LOC100288175 UBE2J2 SAMD11 LOC100130417 LOC105378948 LINC01128 SDF4 RNF223 LINC01342 PERM1 TTLL10 NOC2L MIR200B B3GALT6 C1orf159 FAM41C AGRN FAM132A TNFRSF18 FAM87B KLHL17 TTLL10-AS1 LOC107985728 MIR429 ISG15 MIR200A LOC284600 PLEKHN1 HES4 LINC00115 TNFRSF4
nsv1013524 Chr.1:939510 - 1161955 on Build GRCh38 Gain LOC100288175 AGRN SAMD11 LOC105378948 KLHL17 RNF223 LINC01342 ISG15 PERM1 PLEKHN1 HES4 NOC2L C1orf159
nsv1160644 Chr.1:939652 - 1220663 on Build GRCh38 Deletion LOC100288175 AGRN SAMD11 LOC105378948 TNFRSF18 KLHL17 SDF4 RNF223 LINC01342 TTLL10-AS1 MIR429 ISG15 PERM1 MIR200A TTLL10 PLEKHN1 HES4 NOC2L TNFRSF4 MIR200B C1orf159
nsv544895 Chr.1:917392 - 1054900 on Build GRCh38 Loss PERM1 LOC284600 AGRN SAMD11 PLEKHN1 LOC100130417 HES4 NOC2L KLHL17 LOC107985728 ISG15
dgv2n67 Chr.1:877618 - 1426500 on Build GRCh38 Gain MIR6726 LOC100288175 UBE2J2 SAMD11 CPSF3L LOC100130417 ACAP3 LOC105378948 TAS1R3 SDF4 MIR6808 RNF223 LINC01342 DVL1 PERM1 TTLL10 MIR6727 NOC2L MIR200B MRPL20 LOC148413 B3GALT6 C1orf159 AGRN TMEM88B MXRA8 CPTP FAM132A TNFRSF18 PUSL1 KLHL17 TTLL10-AS1 CCNL2 LOC107985728 MIR429 ISG15 MIR200A LOC284600 AURKAIP1 SCNN1D ANKRD65 PLEKHN1 HES4 TNFRSF4
nsv544898 Chr.1:924665 - 943937 on Build GRCh38 Gain SAMD11 LOC107985728
nsv832980 Chr.1:848279 - 1007037 on Build GRCh38 Gain FAM41C PERM1 LOC284600 SAMD11 PLEKHN1 LOC100130417 HES4 NOC2L LINC01128 KLHL17 LOC107985728

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More Information


Set Membership:

Intragenic Intronic Non-exonic DGV Variation

Panther Classification:

Molecular Function -

chromatin/chromatin-binding, or -regulatory protein

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