accessibility menu, dialog, popup

UserName
Viewing profile as user:

Please enter the information below and press OK to send your cart to Core Services for purchase.

    

System Message

OKCancel
LOADING ...
See other RSL24D1 CNV Assays ›
Gene Symbol
RSL24D1
Assay Reference Genome
Location

Chr.15:55190728 on build GRCh38
Cytoband
15q21.3
Assay ID Hs05365661_cn
Size
Availability Made To Order
Catalog # 4400291
Price 4,505.00
Your Price
Online offer:
4505.0
Check your price ›

Assay Details

Target Gene Details

Entrez Gene ID:

 51187

Gene Name:

 ribosomal L24 domain containing 1

Gene Aliases:

 C15orf15, HRP-L30-iso, L30, RLP24, RPL24, RPL24L, TVAS3

Location:

 Chr.15:55181314-55197033 on Build GRCh38

Assay Gene Location:

 Within Intron 3
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
RSL24D1 NM_016304.2 NP_057388.1
AB462502.1
AF060926.1 AAG43138.1
AF165521.1 AAF86651.1
AF201949.1 AAF17241.1
AF212226.1 AAK26249.1
AK055713.1
AK315431.1
BC008409.1 AAH08409.1
BC008422.1 AAH08422.1
BC008449.1 AAH08449.1
BC008499.1 AAH08499.1
BC009593.1 AAH09593.1
BC009604.1 AAH09604.1
BC012913.1 AAH12913.1
BC014576.1 AAH14576.1
BC016312.1 AAH16312.1
BC016331.1 AAH16331.1
BC016725.1 AAH16725.1
BC016777.1 AAH16777.1
BC026266.1 AAH26266.1
BC026267.1 AAH26267.1
BC028672.1 AAH28672.1
BC035995.1 AAH35995.1
BC093067.1 AAH93067.1
CR457179.1 CAG33460.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
esv2761899 Chr.15:53592144 - 55643724 on Build GRCh38 Gain+Loss LOC107984745 PIGBOS1 PIGB LOC105370829 PYGO1 UNC13C DYX1C1-CCPG1 WDR72 RSL24D1 RAB27A MIR628 PRTG CCPG1 DYX1C1 C15orf65
nsv976937 Chr.15:55190767 - 55191267 on Build GRCh38 Duplication RSL24D1
nsv525768 Chr.15:55173957 - 55193296 on Build GRCh38 Loss RSL24D1
nsv1039471 Chr.15:54845408 - 55260357 on Build GRCh38 Gain RSL24D1 LOC105370829 RAB27A
nsv1043789 Chr.15:55108674 - 55800256 on Build GRCh38 Gain RSL24D1 LOC107984745 PIGBOS1 PIGB PYGO1 RAB27A MIR628 DYX1C1-CCPG1 PRTG CCPG1 DYX1C1 C15orf65

Back To Top

More Information


Additional Information:

For this assay, SNP(s) [rs117520756] 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:

Molecular Function -

ribosomal protein

Gene Ontology Categories:

Function(s) Process(es)


Back To Top

Related Products