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

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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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