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

Chr.1:953038 on build GRCh38
Cytoband
1p36.33
Assay ID Hs03367665_cn
Size
Availability Made To Order
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 9
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
NOC2L NM_015658.3 NP_056473.2
AK022756.1 BAB14230.1
AK024284.1
AK225239.1
AK315080.1
AL050019.1 CAB43240.2
AW749585.1
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 PERM1 PLEKHN1 ISG15 NOC2L LOC107985728 LOC100130417 LOC284600 KLHL17 LOC100288175 RNF223 HES4 AGRN C1orf159 LOC105378948 SAMD11
nsv482937 Chr.1:10001 - 2368561 on Build GRCh38 Loss MIR1302-2 PLEKHN1 MIR6859-2 MMP23A PUSL1 ATAD3B MORN1 SLC35E2 LOC148413 MIR429 SAMD11 MIR200B ATAD3A MIB2 OR4F29 ISG15 FAAP20 TTLL10 LOC100506504 KLHL17 TTLL10-AS1 TMEM240 LOC105378592 ATAD3C MXRA8 LOC102725121 AGRN PERM1 LOC107985728 LOC284600 ACAP3 CDK11B LOC105378591 LOC100133331 SSU72 ANKRD65 SCNN1D FAM41C MTND2P28 PRKCZ LOC102724312 FNDC10 VWA1 FAM132A LOC105378948 B3GALT6 LOC100132287 TMEM52 OR4F16 NOC2L LOC100130417 MIR6727 FAM138A CFAP74 SDF4 LOC100288175 LINC01128 CCNL2 MRPL20 MIR6726 LOC105378589 LOC105378949 MTND1P23 TAS1R3 MIR200A CPSF3L LINC01342 LOC729737 LINC00115 MMP23B DDX11L1 MIR6723 TMEM88B RNF223 HES4 CALML6 MIR6859-1 FAM87B NADK LOC100287934 LOC100129534 GABRD LOC107985729 UBE2J2 CDK11A C1orf159 LOC100134822 SKI MIR6808 DVL1 CPTP AURKAIP1 TNFRSF4 WASH7P OR4F5 GNB1 LOC100288069 TNFRSF18 LOC101928626 LOC107984841 LOC105378947 SLC35E2B
nsv950451 Chr.1:899421 - 1094520 on Build GRCh38 Deletion PERM1 PLEKHN1 ISG15 NOC2L LOC107985728 LOC100130417 LOC284600 KLHL17 LOC100288175 RNF223 HES4 AGRN C1orf159 LOC105378948 SAMD11
nsv509035 Chr.1:891406 - 985724 on Build GRCh38 Insertion PERM1 PLEKHN1 NOC2L LOC107985728 LOC100130417 LOC284600 KLHL17 SAMD11
nsv428334 Chr.1:874371 - 1220569 on Build GRCh38 Gain PERM1 PLEKHN1 NOC2L LOC107985728 LOC100130417 LOC284600 SDF4 LOC100288175 C1orf159 MIR429 FAM41C SAMD11 MIR200B ISG15 TNFRSF4 MIR200A LINC01342 TTLL10 KLHL17 TTLL10-AS1 RNF223 TNFRSF18 HES4 AGRN LOC105378948
nsv10161 Chr.1:776731 - 1777210 on Build GRCh38 Gain+Loss PLEKHN1 NOC2L MMP23A LOC100130417 MIR6727 PUSL1 SDF4 ATAD3B LOC100288175 LINC01128 SLC35E2 LOC148413 MIR429 CCNL2 MRPL20 MIR6726 SAMD11 MIR200B ATAD3A MIB2 ISG15 TAS1R3 MIR200A CPSF3L LINC01342 TTLL10 LINC00115 KLHL17 MMP23B TTLL10-AS1 TMEM88B RNF223 TMEM240 ATAD3C HES4 MXRA8 AGRN FAM87B NADK LOC100287934 PERM1 LOC107985728 LOC284600 ACAP3 CDK11B LOC107985729 UBE2J2 CDK11A SSU72 ANKRD65 C1orf159 SCNN1D FAM41C MIR6808 DVL1 CPTP AURKAIP1 TNFRSF4 LOC102724312 LOC100288069 FNDC10 VWA1 TNFRSF18 FAM132A LOC105378948 B3GALT6 SLC35E2B
dgv5n100 Chr.1:585989 - 1114424 on Build GRCh38 Gain PERM1 PLEKHN1 OR4F16 NOC2L LOC107985728 LOC100130417 LOC284600 LOC100133331 LOC100288175 LINC01128 C1orf159 FAM41C SAMD11 MTND2P28 ISG15 MTND1P23 LINC00115 KLHL17 MIR6723 LOC100288069 RNF223 HES4 AGRN LOC101928626 LOC107984841 FAM87B LOC105378948 LOC105378947 LOC100287934
nsv517709 Chr.1:817186 - 1275912 on Build GRCh38 Gain+Loss PERM1 PLEKHN1 NOC2L LOC107985728 LOC100130417 LOC284600 UBE2J2 SDF4 LOC100288175 LINC01128 C1orf159 MIR429 FAM41C SAMD11 MIR200B ISG15 TNFRSF4 MIR200A LINC01342 TTLL10 LINC00115 KLHL17 TTLL10-AS1 RNF223 TNFRSF18 HES4 AGRN FAM132A FAM87B LOC105378948 B3GALT6
nsv1013524 Chr.1:939510 - 1161955 on Build GRCh38 Gain PERM1 PLEKHN1 ISG15 NOC2L LINC01342 KLHL17 LOC100288175 RNF223 HES4 AGRN C1orf159 LOC105378948 SAMD11
nsv1160644 Chr.1:939652 - 1220663 on Build GRCh38 Deletion PERM1 PLEKHN1 ISG15 NOC2L TNFRSF4 MIR200A LINC01342 TTLL10 KLHL17 SDF4 TTLL10-AS1 LOC100288175 RNF223 TNFRSF18 HES4 AGRN C1orf159 MIR429 LOC105378948 SAMD11 MIR200B
nsv544895 Chr.1:917392 - 1054900 on Build GRCh38 Loss PERM1 PLEKHN1 ISG15 NOC2L LOC107985728 HES4 LOC100130417 AGRN LOC284600 KLHL17 SAMD11
dgv2n67 Chr.1:877618 - 1426500 on Build GRCh38 Gain PERM1 PLEKHN1 NOC2L LOC107985728 LOC100130417 LOC284600 ACAP3 MIR6727 UBE2J2 PUSL1 SDF4 LOC100288175 LOC148413 ANKRD65 C1orf159 MIR429 CCNL2 MRPL20 SCNN1D MIR6726 SAMD11 MIR200B MIR6808 DVL1 CPTP ISG15 AURKAIP1 TAS1R3 TNFRSF4 MIR200A CPSF3L LINC01342 TTLL10 KLHL17 TTLL10-AS1 TMEM88B RNF223 TNFRSF18 HES4 MXRA8 AGRN FAM132A LOC105378948 B3GALT6
nsv832980 Chr.1:848279 - 1007037 on Build GRCh38 Gain PERM1 PLEKHN1 LINC01128 NOC2L LOC107985728 HES4 LOC100130417 LOC284600 FAM41C KLHL17 SAMD11

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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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