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

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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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