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

Chr.1:999689 on build GRCh38
Cytoband
1p36.33
Assay ID Hs03009663_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 1
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
DB485006.1 1 407

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

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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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