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See other HES4 CNV Assays ›
Gene Symbol
HES4
Assay Reference Genome
Location

Chr.1:998984 on build GRCh38
Cytoband
1p36.33
Assay ID Hs03334241_cn
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Catalog # 4400291
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  • Genomic Map
  • Assay Details
  • More Information

Genomic Map

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Assay Details

Target Gene Details

Entrez Gene ID:

57801

Gene Name:

hes family bHLH transcription factor 4

Gene Aliases:

bHLHb42

Location:

Chr.1:998962-1001052 on Build GRCh38

Assay Gene Location:

Overlaps - Exon 3
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
HES4 NM_001142467.1 NP_001135939.1
NM_021170.3 NP_066993.1
XM_005244771.4 XP_005244828.1
BC012351.1 AAH12351.1
BM128269.1

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 C1orf159 RNF223 SAMD11 AGRN PERM1 ISG15 LOC284600 HES4 LOC100130417 NOC2L KLHL17 LOC105378948 LOC107985728 LOC100288175 PLEKHN1
nsv482937 Chr.1:10001 - 2368561 on Build GRCh38 Loss LINC01342 LOC100506504 MIR6727 LINC00115 FAM41C MIR1302-2 ATAD3B CCNL2 MTND1P23 LOC107985728 MTND2P28 C1orf159 MIR200A CDK11A CFAP74 CALML6 TMEM52 OR4F5 LOC100130417 LOC101928626 ATAD3C B3GALT6 ACAP3 LOC100129534 LOC105378591 LOC105378948 LOC105378592 FAM87B LOC100288175 LOC729737 SSU72 RNF223 LOC105378949 MIR6726 SDF4 TTLL10 LOC148413 AURKAIP1 TAS1R3 NOC2L CPTP MIR6859-1 LOC100133331 NADK SAMD11 TMEM240 DDX11L1 LOC100287934 MXRA8 KLHL17 WASH7P MIR200B MIR6723 SCNN1D MORN1 FAM132A TTLL10-AS1 PUSL1 OR4F16 LOC107985729 OR4F29 CPSF3L FAAP20 TNFRSF4 UBE2J2 TMEM88B ANKRD65 AGRN CDK11B DVL1 LOC284600 HES4 VWA1 MIR6859-2 MMP23B SLC35E2B LOC105378589 PLEKHN1 PRKCZ GABRD PERM1 LOC100288069 MIR6808 SLC35E2 MRPL20 MIR429 FNDC10 ATAD3A LOC105378947 LOC100134822 LOC102725121 FAM138A LINC01128 MIB2 LOC100132287 ISG15 GNB1 LOC102724312 MMP23A LOC107984841 TNFRSF18 SKI
nsv950451 Chr.1:899421 - 1094520 on Build GRCh38 Deletion C1orf159 RNF223 SAMD11 AGRN PERM1 ISG15 LOC284600 HES4 LOC100130417 NOC2L KLHL17 LOC105378948 LOC107985728 LOC100288175 PLEKHN1
nsv428334 Chr.1:874371 - 1220569 on Build GRCh38 Gain LINC01342 RNF223 FAM41C SDF4 PERM1 TTLL10 NOC2L MIR429 LOC107985728 TNFRSF4 C1orf159 MIR200A SAMD11 AGRN ISG15 LOC284600 HES4 LOC100130417 TNFRSF18 KLHL17 LOC105378948 MIR200B LOC100288175 PLEKHN1 TTLL10-AS1
dgv5n100 Chr.1:585989 - 1114424 on Build GRCh38 Gain RNF223 LINC00115 OR4F16 FAM41C PERM1 LOC100288069 MTND1P23 NOC2L LOC105378947 LOC107985728 MTND2P28 C1orf159 LOC100133331 SAMD11 AGRN LINC01128 ISG15 LOC284600 HES4 LOC100130417 LOC101928626 LOC100287934 LOC107984841 KLHL17 LOC105378948 FAM87B MIR6723 LOC100288175 PLEKHN1
nsv10161 Chr.1:776731 - 1777210 on Build GRCh38 Gain+Loss LINC01342 MIR6727 PUSL1 LINC00115 FAM41C LOC107985729 ATAD3B CCNL2 CPSF3L LOC107985728 TNFRSF4 UBE2J2 C1orf159 MIR200A TMEM88B CDK11A ANKRD65 AGRN CDK11B DVL1 LOC284600 HES4 LOC100130417 VWA1 ATAD3C B3GALT6 ACAP3 LOC105378948 MMP23B FAM87B SLC35E2B LOC100288175 PLEKHN1 SSU72 RNF223 MIR6726 SDF4 PERM1 TTLL10 LOC100288069 LOC148413 MIR6808 AURKAIP1 SLC35E2 TAS1R3 MRPL20 NOC2L CPTP MIR429 FNDC10 ATAD3A NADK SAMD11 LINC01128 TMEM240 MIB2 ISG15 LOC100287934 LOC102724312 MMP23A TNFRSF18 MXRA8 KLHL17 MIR200B SCNN1D FAM132A TTLL10-AS1
nsv517709 Chr.1:817186 - 1275912 on Build GRCh38 Gain+Loss LINC01342 RNF223 LINC00115 FAM41C SDF4 PERM1 TTLL10 NOC2L MIR429 LOC107985728 TNFRSF4 UBE2J2 C1orf159 MIR200A SAMD11 AGRN LINC01128 ISG15 LOC284600 HES4 LOC100130417 B3GALT6 TNFRSF18 KLHL17 LOC105378948 MIR200B FAM87B LOC100288175 FAM132A PLEKHN1 TTLL10-AS1
nsv827252 Chr.1:998725 - 1001127 on Build GRCh38 Gain HES4
nsv1013524 Chr.1:939510 - 1161955 on Build GRCh38 Gain C1orf159 LINC01342 RNF223 SAMD11 AGRN PERM1 ISG15 HES4 NOC2L KLHL17 LOC105378948 LOC100288175 PLEKHN1
dgv2n67 Chr.1:877618 - 1426500 on Build GRCh38 Gain LINC01342 MIR6727 RNF223 PUSL1 MIR6726 SDF4 PERM1 TTLL10 LOC148413 MIR6808 AURKAIP1 TAS1R3 MRPL20 CCNL2 CPSF3L NOC2L CPTP MIR429 LOC107985728 TNFRSF4 UBE2J2 C1orf159 MIR200A TMEM88B ANKRD65 SAMD11 AGRN DVL1 ISG15 LOC284600 HES4 LOC100130417 B3GALT6 TNFRSF18 ACAP3 MXRA8 KLHL17 LOC105378948 MIR200B SCNN1D LOC100288175 FAM132A PLEKHN1 TTLL10-AS1
nsv544895 Chr.1:917392 - 1054900 on Build GRCh38 Loss LOC284600 HES4 LOC100130417 NOC2L KLHL17 SAMD11 AGRN PERM1 LOC107985728 ISG15 PLEKHN1
nsv1160644 Chr.1:939652 - 1220663 on Build GRCh38 Deletion C1orf159 LINC01342 MIR200A RNF223 SDF4 SAMD11 AGRN PERM1 TTLL10 ISG15 HES4 NOC2L MIR429 TNFRSF18 KLHL17 LOC105378948 MIR200B TNFRSF4 LOC100288175 PLEKHN1 TTLL10-AS1
nsv832980 Chr.1:848279 - 1007037 on Build GRCh38 Gain LOC284600 HES4 LOC100130417 NOC2L FAM41C KLHL17 SAMD11 PERM1 LINC01128 LOC107985728 PLEKHN1

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More Information


Set Membership:

Intragenic Non-exonic DGV Variation

Panther Classification:

Molecular Function -

basic helix-loop-helix transcription factor

Gene Ontology Categories:

Function(s) Process(es)

transcription, DNA-templated
regulation of transcription, DNA-templated
nervous system development
cell differentiation
DNA binding
transcription factor binding
protein dimerization activity

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