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

Chr.1:999577 on build GRCh38
Cytoband
1p36.33
Assay ID Hs00272009_cn
Size
Availability Made To Order
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 Intron 1 - Exon 2
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
AB048791.1 BAB13510.1
BC012351.1 AAH12351.1
BI757407.1

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