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

Chr.19:2250274 on build GRCh38
Cytoband
19p13.3
Assay ID Hs02980087_cn
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Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 268

Gene Name:

 anti-Mullerian hormone

Gene Aliases:

 MIF, MIS

Location:

 Chr.19:2249114-2252073 on Build GRCh38

Assay Gene Location:

 Within Intron 1
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
AMH NM_000479.3 NP_000470.2
BC049194.1 AAH49194.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv578382 Chr.19:2194897 - 2260362 on Build GRCh38 Loss SF3A2 AMH MIR6789 MIR1227 MIR4321 JSRP1 DOT1L LOC105372239 PLEKHJ1
dgv6218n54 Chr.19:2221793 - 2336009 on Build GRCh38 Loss LSM7 MIR4321 DOT1L SPPL2B LINGO3 SF3A2 AMH MIR6789 MIR1227 C19orf35 JSRP1 OAZ1 LOC105372239 PLEKHJ1
nsv578383 Chr.19:2214058 - 2285197 on Build GRCh38 Loss SF3A2 AMH MIR6789 MIR1227 MIR4321 C19orf35 JSRP1 DOT1L OAZ1 LOC105372239 PLEKHJ1
nsv833707 Chr.19:2187092 - 2372223 on Build GRCh38 Loss LSM7 MIR4321 DOT1L SPPL2B LINGO3 SF3A2 AMH MIR6789 MIR1227 C19orf35 JSRP1 OAZ1 LOC105372239 PLEKHJ1

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More Information


Additional Information:

For this assay, SNP(s) [rs77671243] 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

Gene Ontology Categories:

Function(s) Process(es)


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