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See other ZMYM2 CNV Assays ›
Gene Symbol
ZMYM2
Assay Reference Genome
Location

Chr.13:20005146 on build GRCh38
Cytoband
13q12.11
Assay ID Hs02913620_cn
Size
Availability Made To Order
Catalog # 4400291
Price 4,505.00
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Assay Details

Target Gene Details

Entrez Gene ID:

 7750

Gene Name:

 zinc finger MYM-type containing 2

Gene Aliases:

 FIM, MYM, RAMP, SCLL, ZNF198

Location:

 Chr.13:19957412-20091845 on Build GRCh38

Assay Gene Location:

 Within Exon 10
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
ZMYM2 NM_001190964.2 6 1396 NP_001177893.1
NM_001190965.2 5 1411 NP_001177894.1
NM_003453.4 6 1504 NP_003444.1
NM_197968.3 5 1457 NP_932072.1
XM_005266520.3 5 1416 XP_005266577.1
XM_011535216.2 6 1086 XP_011533518.1
XM_011535222.1 5 1347 XP_011533524.1
XM_017020728.1 5 1347 XP_016876217.1
XM_017020729.1 5 1322 XP_016876218.1
XM_017020731.1 6 1139 XP_016876220.1
XM_017020732.1 6 1161 XP_016876221.1
XM_017020733.1 7 1188 XP_016876222.1
XM_017020734.1 7 1174 XP_016876223.1
XM_017020735.1 6 1138 XP_016876224.1
XM_017020736.1 6 1310 XP_016876225.1
XM_017020737.1 6 1085 XP_016876226.1
XM_017020738.1 5 1400 XP_016876227.1
XM_017020739.1 5 1347 XP_016876228.1
AF035374.1 3 702 AAB88464.1
AF060181.1 3 754 AAC23591.1
AJ224901.1 6 1390 CAA12204.1
AK226118.1 5 1392
AK289741.1 5 1382
AK302917.1
AL136621.1 6 1190 CAB66556.2
BC036372.1 5 1457 AAH36372.1
BX647944.1 5 1411 CAH56193.1
Y13472.1 6 1396 CAA73875.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv832557 Chr.13:19910435 - 20081915 on Build GRCh38 Gain ZMYM2
nsv561215 Chr.13:19871303 - 20076371 on Build GRCh38 Gain ZMYM2
esv2761244 Chr.13:19389134 - 20043200 on Build GRCh38 Gain LINC00350 ZMYM5 TPTE2 ZMYM2 MPHOSPH8 PSPC1
nsv1046946 Chr.13:19730301 - 20507454 on Build GRCh38 Gain ZMYM5 GJB2 GJB6 LINC01072 CRYL1 MIR4499 ZMYM2 PSPC1 GJA3
esv3892297 Chr.13:19803308 - 20022425 on Build GRCh38 Gain ZMYM5 ZMYM2

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More Information


Additional Information:

For this assay, SNP(s) [rs115819790] 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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