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

Chr.1:1000633 on build GRCh38
Cytoband
1p36.33
Assay ID Hs03377591_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:

Within Exon 1
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
HES4 XM_005244771.4 1 420 XP_005244828.1

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

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More Information


Set Membership:

Intragenic 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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