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

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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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