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Gene Symbol
CRYM
Assay Reference Genome
Location

Chr.16:21260802 on build GRCh38
Cytoband
16p12.2
Assay ID Hs05454104_cn
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Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 1428

Gene Name:

 crystallin mu

Gene Aliases:

 DFNA40, THBP

Location:

 Chr.16:21258518-21303136 on Build GRCh38

Assay Gene Location:

 Within Intron 9
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
CRYM NM_001888.4 NP_001879.1
AK290852.1
AK310424.1
BC018061.1 AAH18061.1
BX648477.1 CAI46030.1
L02950.1 AAC16914.1
U85772.1 AAB81564.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
esv3638165 Chr.16:21188383 - 21267495 on Build GRCh38 Gain ANKS4B CRYM ZP2
nsv571623 Chr.16:21084049 - 21341186 on Build GRCh38 Gain ANKS4B DNAH3 CRYM ZP2 CRYM-AS1 TMEM159
esv3638164 Chr.16:21185596 - 21338776 on Build GRCh38 Gain ANKS4B CRYM ZP2 CRYM-AS1
nsv436835 Chr.16:18930652 - 21500976 on Build GRCh38 Insertion LOC100190986 THUMPD1 SNX29P1 SMG1P3 ITPRIPL2 SYT17 ACSM2A CRYM-AS1 GP2 COQ7 NPIPB3 ACSM1 KNOP1 TMEM159 LYRM1 ACSM5 ERI2 ACSM3 GPRC5B UMOD LOC102723385 C16orf62 ACSM2B ANKS4B DNAH3 CRYM DCUN1D3 GDE1 CCP110 ZP2 TMC5 LOC81691 PDILT GPR139 IQCK TMC7 CLEC19A

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More Information


Additional Information:

For this assay, SNP(s) [rs73539733] 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 Intronic Non-exonic DGV Variation

Panther Classification:

Gene Ontology Categories:

Function(s) Process(es)


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