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

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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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