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Gene Symbol
MVD
Assay Reference Genome
Location

Chr.16:88652095 on build GRCh38
Cytoband
16q24.2
Assay ID Hs01435828_cn
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Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 4597

Gene Name:

 mevalonate diphosphate decarboxylase

Gene Aliases:

 FP17780, MDDase, MPD, POROK7

Location:

 Chr.16:88651935-88663153 on Build GRCh38

Assay Gene Location:

 Within Exon 13
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
MVD NM_002461.2 10 1702 NP_002452.1
XM_011523086.2 11 1808 XP_011521388.1
XM_011523087.2 12 1813 XP_011521389.1
XM_011523088.2 11 1709 XP_011521390.1
XM_011523089.2 13 1929 XP_011521391.1
AY203927.1 6 2193 AAP34450.1
BC000011.2 10 1663 AAH00011.1
U49260.1 10 1640 AAC50440.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1926 Chr.16:88626290 - 88660544 on Build GRCh38 Insertion ZC3H18 CYBA IL17C MVD
nsv471113 Chr.16:88650665 - 88764428 on Build GRCh38 Loss LOC339059 CYBA CTU2 SNAI3-AS1 RNF166 SNAI3 MVD LOC100289580 MIR4722 PIEZO1
esv3639554 Chr.16:88641322 - 88654848 on Build GRCh38 Loss CYBA MVD
nsv833325 Chr.16:88553738 - 88698194 on Build GRCh38 Loss ZC3H18 CYBA SNAI3-AS1 ZC3H18-AS1 IL17C RNF166 SNAI3 MVD
nsv952070 Chr.16:88257295 - 88780192 on Build GRCh38 Deletion LOC339059 ZC3H18 CTU2 SNAI3-AS1 ZC3H18-AS1 MVD LOC100289580 MIR5189 PIEZO1 LOC107984862 CYBA IL17C RNF166 SNAI3 MIR4722 ZNF469 ZFPM1
nsv482951 Chr.16:88633593 - 90228345 on Build GRCh38 Loss PRDM7 SPATA2L LOC105371409 CHMP1A ANKRD11 ACSF3 DEF8 LOC105371419 GALNS IL17C APRT SPG7 SNORD68 FANCA PABPN1L LOC107987238 TRAPPC2L ZNF276 CDK10 RNF166 SNAI3 LOC400558 LOC101927817 SPIRE2 CTU2 SNAI3-AS1 ZNF778 VPS9D1-AS1 VPS9D1 GAS8 TUBB8P7 CYBA AFG3L1P CDH15 LOC107984817 SLC22A31 LOC339059 GAS8-AS1 CPNE7 FAM157C MVD LOC100289580 TCF25 CENPBD1 LOC105371414 DPEP1 PIEZO1 URAHP LOC100287036 CDT1 SPATA33 RPL13 LINC00304 DBNDD1 CBFA2T3 MC1R LOC100129697 MIR4722 TUBB3 LOC101927793

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More Information


Additional Information:

For this assay, SNP(s) [rs80283791] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Set Membership:

 Intragenic Exonic DGV Variation

Panther Classification:

Gene Ontology Categories:

Function(s) Process(es)


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