Please enter the information below and press OK to send your cart to Core Services for purchase.

    

System Message

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

Chr.1:925973 on build GRCh38
Cytoband
1p36.33
Assay ID Hs01186397_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

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:

 Overlaps Intron 1 - Intron 2
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
SAMD11 NM_152486.2 NP_689699.2
CN342795.1
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
esv2762302 Chr.1:914637 - 1106320 on Build GRCh38 Gain LOC105378948 NOC2L SAMD11 LOC100288175 LOC100130417 LOC284600 RNF223 KLHL17 C1orf159 ISG15 PLEKHN1 PERM1 LOC107985728 HES4 AGRN
nsv482937 Chr.1:10001 - 2368561 on Build GRCh38 Loss FAM138A TNFRSF18 MIR1302-2 CDK11A FAM132A MIB2 PERM1 MTND1P23 TMEM88B HES4 LOC105378948 LOC105378592 TAS1R3 MORN1 CDK11B ATAD3C SKI FNDC10 LOC100288175 SDF4 LINC00115 RNF223 KLHL17 LINC01128 DDX11L1 LOC729737 OR4F5 TMEM240 ANKRD65 LOC107985729 TTLL10-AS1 VWA1 MMP23B PUSL1 CALML6 MIR6859-2 LOC102725121 MIR429 SLC35E2B LOC107985728 OR4F16 PRKCZ FAM41C NOC2L CCNL2 MTND2P28 LOC100287934 MIR6726 LOC101928626 CFAP74 LOC107984841 ATAD3B SCNN1D GNB1 LOC100133331 AGRN MMP23A UBE2J2 MIR6727 LOC100288069 WASH7P CPTP SLC35E2 FAM87B LINC01342 SSU72 OR4F29 LOC105378947 AURKAIP1 LOC100134822 MXRA8 DVL1 LOC100130417 LOC100506504 C1orf159 NADK ISG15 LOC105378589 PLEKHN1 ATAD3A MRPL20 LOC105378949 TNFRSF4 CPSF3L LOC148413 TMEM52 LOC284600 FAAP20 MIR200B TTLL10 MIR6808 LOC100132287 MIR200A GABRD MIR6859-1 MIR6723 B3GALT6 SAMD11 LOC102724312 LOC100129534 ACAP3 LOC105378591
nsv950451 Chr.1:899421 - 1094520 on Build GRCh38 Deletion LOC105378948 NOC2L SAMD11 LOC100288175 LOC100130417 LOC284600 RNF223 KLHL17 C1orf159 ISG15 PLEKHN1 PERM1 LOC107985728 HES4 AGRN
nsv509035 Chr.1:891406 - 985724 on Build GRCh38 Insertion NOC2L SAMD11 PLEKHN1 PERM1 LOC107985728 LOC100130417 LOC284600 KLHL17
dgv9n54 Chr.1:925754 - 952840 on Build GRCh38 Loss NOC2L SAMD11
nsv428334 Chr.1:874371 - 1220569 on Build GRCh38 Gain TNFRSF4 TNFRSF18 TTLL10-AS1 LOC284600 MIR200B LINC01342 TTLL10 MIR429 PERM1 LOC107985728 MIR200A HES4 LOC105378948 FAM41C NOC2L SAMD11 LOC100288175 SDF4 LOC100130417 RNF223 KLHL17 C1orf159 ISG15 PLEKHN1 AGRN
dgv5n100 Chr.1:585989 - 1114424 on Build GRCh38 Gain LOC100288069 FAM87B LOC284600 PERM1 LOC107985728 MTND1P23 OR4F16 HES4 LOC105378948 FAM41C LOC105378947 MIR6723 NOC2L SAMD11 MTND2P28 LOC100288175 LOC100287934 LOC100130417 LINC00115 LOC101928626 RNF223 KLHL17 LOC107984841 C1orf159 LINC01128 ISG15 PLEKHN1 LOC100133331 AGRN
nsv10161 Chr.1:776731 - 1777210 on Build GRCh38 Gain+Loss TNFRSF18 MMP23A UBE2J2 MIR6727 LOC100288069 CPTP SLC35E2 FAM87B LINC01342 CDK11A FAM132A MIB2 PERM1 TMEM88B HES4 SSU72 LOC105378948 TAS1R3 AURKAIP1 CDK11B ATAD3C MXRA8 DVL1 FNDC10 LOC100288175 SDF4 LOC100130417 LINC00115 RNF223 KLHL17 C1orf159 LINC01128 NADK ISG15 PLEKHN1 ATAD3A MRPL20 TMEM240 TNFRSF4 ANKRD65 CPSF3L LOC107985729 TTLL10-AS1 LOC148413 VWA1 LOC284600 MMP23B MIR200B PUSL1 TTLL10 MIR6808 MIR429 SLC35E2B LOC107985728 MIR200A FAM41C NOC2L B3GALT6 SAMD11 CCNL2 LOC102724312 LOC100287934 MIR6726 ATAD3B SCNN1D ACAP3 AGRN
dgv1n111 Chr.1:690090 - 939522 on Build GRCh38 Duplication FAM41C SAMD11 LOC100288069 LOC100287934 LOC100130417 FAM87B LINC00115 LOC284600 LOC107984841 LINC01128 LOC100133331 LOC107985728 OR4F16
nsv517709 Chr.1:817186 - 1275912 on Build GRCh38 Gain+Loss TNFRSF4 TNFRSF18 UBE2J2 TTLL10-AS1 FAM87B LOC284600 MIR200B LINC01342 TTLL10 FAM132A MIR429 PERM1 LOC107985728 MIR200A HES4 LOC105378948 FAM41C NOC2L B3GALT6 SAMD11 LOC100288175 SDF4 LOC100130417 LINC00115 RNF223 KLHL17 C1orf159 LINC01128 ISG15 PLEKHN1 AGRN
dgv3n111 Chr.1:783283 - 939522 on Build GRCh38 Duplication FAM41C LINC01128 SAMD11 LOC100287934 LOC107985728 LOC100130417 FAM87B LINC00115 LOC284600
dgv6n54 Chr.1:917392 - 934930 on Build GRCh38 Loss SAMD11 LOC107985728 LOC100130417 LOC284600
dgv2n67 Chr.1:877618 - 1426500 on Build GRCh38 Gain TNFRSF4 ANKRD65 TNFRSF18 UBE2J2 CPSF3L TTLL10-AS1 MIR6727 LOC148413 CPTP LOC284600 MIR200B LINC01342 PUSL1 TTLL10 MIR6808 FAM132A MIR429 PERM1 LOC107985728 TMEM88B MIR200A HES4 LOC105378948 TAS1R3 AURKAIP1 NOC2L B3GALT6 SAMD11 CCNL2 MXRA8 DVL1 LOC100288175 SDF4 LOC100130417 MIR6726 RNF223 KLHL17 C1orf159 ISG15 SCNN1D PLEKHN1 ACAP3 MRPL20 AGRN
nsv544898 Chr.1:924665 - 943937 on Build GRCh38 Gain SAMD11 LOC107985728
nsv832980 Chr.1:848279 - 1007037 on Build GRCh38 Gain FAM41C LINC01128 NOC2L SAMD11 PLEKHN1 PERM1 LOC107985728 LOC100130417 LOC284600 HES4 KLHL17

Back To Top

More Information


Set Membership:

 Intragenic Intronic Non-exonic DGV Variation

Panther Classification:


Back To Top

Related Products