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

Chr.17:82425639 on build GRCh38
Cytoband
17q25.3
Assay ID Hs03981278_cn
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Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 284004

Gene Name:

 hexosaminidase D

Gene Aliases:

 -

Location:

 Chr.17:82418376-82442645 on Build GRCh38

Assay Gene Location:

 Within Intron 3
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
HEXDC NM_173620.2 NP_775891.2
XM_005256346.3 XP_005256403.1
XM_005256347.4 XP_005256404.1
XM_006722280.3 XP_006722343.1
XM_011523561.2 XP_011521863.1
XM_017024484.1 XP_016879973.1
XM_017024485.1 XP_016879974.1
AK074405.1 BAB85072.1
BC018205.1 AAH18205.2
BC035561.1 AAH35561.1
FM204887.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1160502 Chr.17:82411695 - 82526070 on Build GRCh38 Deletion NARF C17orf62 HEXDC OGFOD3 FOXK2
nsv1062980 Chr.17:82408938 - 82687942 on Build GRCh38 Gain MIR4525 NARF C17orf62 HEXDC OGFOD3 FOXK2 RAB40B WDR45B
nsv428351 Chr.17:81152631 - 83064073 on Build GRCh38 Gain TBCD FASN SECTM1 MYADML2 GPS1 MAFG-AS1 BAHCC1 LOC105376790 SIRT7 GCGR CCDC57 SLC38A10 ANAPC11 PDE6G ARL16 LINC00482 CD7 SNORD134 AATK UTS2R DCXR MIR4740 TEX19 TEPSIN NOTUM DUS1L FAAP100 CEP131 HGS MIR4525 MIR6787 C17orf62 SLC25A10 FOXK2 ARHGDIA LOC101929552 NPLOC4 SLC16A3 FN3K PCYT2 NARF TSPAN10 MCRIP1 NPB ZNF750 RAB40B FSCN2 LOC100130370 B3GNTL1 RFNG ACTG1 LOC105371944 HEXDC OGFOD3 C17orf89 MAFG WDR45B AATK-AS1 P4HB OXLD1 MRPL12 RAC3 LOC105371925 ALYREF PPP1R27 TMEM105 LOC101929511 STRA13 FN3KRP CCDC137 ASPSCR1 MIR6786 CSNK1D LOC105376791 LRRC45 PYCR1 MIR3186
nsv1067160 Chr.17:82381853 - 82446450 on Build GRCh38 Loss C17orf62 HEXDC OGFOD3 LOC105376790
nsv828143 Chr.17:82400094 - 82429642 on Build GRCh38 Loss HEXDC OGFOD3
nsv469561 Chr.17:82251148 - 82472274 on Build GRCh38 Loss LOC101929511 TEX19 NARF SECTM1 C17orf62 HEXDC CSNK1D OGFOD3 CD7 UTS2R LOC105376790
nsv833574 Chr.17:82419054 - 82579254 on Build GRCh38 Gain NARF C17orf62 HEXDC FOXK2
nsv1067194 Chr.17:82294731 - 82653129 on Build GRCh38 Gain TEX19 NARF SECTM1 C17orf62 HEXDC OGFOD3 FOXK2 CD7 UTS2R LOC105376790 WDR45B
esv2762577 Chr.17:82244836 - 82838431 on Build GRCh38 Gain+Loss TBCD TEX19 NARF SECTM1 ZNF750 RAB40B LOC105376790 LOC101929511 MIR4525 FN3KRP C17orf62 HEXDC CSNK1D OGFOD3 FOXK2 LOC105376791 CD7 LOC101929552 UTS2R FN3K WDR45B
esv21913 Chr.17:81828123 - 83103548 on Build GRCh38 Gain+Loss TBCD FASN SECTM1 MYADML2 GPS1 MAFG-AS1 LOC105376790 SIRT7 CCDC57 ANAPC11 CD7 SNORD134 UTS2R DCXR TEX19 NOTUM DUS1L METRNL MIR4525 MIR6787 C17orf62 FOXK2 ARHGDIA LOC101929552 SLC16A3 FN3K PCYT2 NARF MCRIP1 NPB ZNF750 RAB40B B3GNTL1 RFNG LOC105371944 HEXDC OGFOD3 MAFG WDR45B P4HB RAC3 ALYREF PPP1R27 LOC101929511 STRA13 FN3KRP ASPSCR1 CSNK1D LOC105376791 LRRC45 PYCR1

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More Information


Set Membership:

 Intragenic Intronic Non-exonic DGV Variation

Gene Ontology Categories:

Function(s) Process(es)


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