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See other NOC2L CNV Assays ›
Gene Symbol
NOC2L
Assay Reference Genome
Location

Chr.1:954155 on build GRCh38
Cytoband
1p36.33
Assay ID Hs03348105_cn
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Catalog # 4400291
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  • Genomic Map
  • Assay Details
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Genomic Map

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Assay Details

Target Gene Details

Entrez Gene ID:

26155

Gene Name:

NOC2 like nucleolar associated transcriptional repressor

Gene Aliases:

NET15, NET7, NIR, PPP1R112

Location:

Chr.1:944203-959299 on Build GRCh38

Assay Gene Location:

Within Intron 6
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
NOC2L NM_015658.3 NP_056473.2
AK024284.1
AK225239.1
AK315080.1
AL050019.1 CAB43240.2
BC003555.1 AAH03555.1

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

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More Information


Set Membership:

Intragenic Intronic Non-exonic DGV Variation

Gene Ontology Categories:

Function(s) Process(es)

negative regulation of transcription from RNA polymerase II promoter
negative regulation of B cell apoptotic process
transcription, DNA-templated
apoptotic process
chromatin assembly
nucleolus to nucleoplasm transport
cellular response to UV
negative regulation of histone acetylation
ribosomal large subunit biogenesis
regulation of signal transduction by p53 class mediator
negative regulation of intrinsic apoptotic signaling pathway
chromatin binding
transcription corepressor activity
protein binding
nucleosome binding
histone binding
poly(A) RNA binding
repressing transcription factor binding

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