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 CHRNB1 CNV Assays ›
Gene Symbol
CHRNB1
Assay Reference Genome
Location

Chr.17:7455341 on build GRCh38
Cytoband
17p13.1
Assay ID Hs01141596_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

Assay Details

Target Gene Details

Entrez Gene ID:

 1140

Gene Name:

 cholinergic receptor nicotinic beta 1 subunit

Gene Aliases:

 ACHRB, CHRNB, CMS1D, CMS2A, CMS2C, SCCMS

Location:

 Chr.17:7445087-7457613 on Build GRCh38

Assay Gene Location:

 Within Exon 9
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
CHRNB1 NM_000747.2 9 1143 NP_000738.2
AK294880.1 6 2040
AK298938.1 8 997
AK308106.1 9 1132
BC011371.1 9 1131 AAH11371.1
BC023553.2 9 1143 AAH23553.1
X14830.1 9 1118 CAA32939.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
esv2422288 Chr.17:6789933 - 7646709 on Build GRCh38 Deletion ELP5 DLG4 POLR2A SPEM1 ZBTB4 EIF5A SENP3-EIF4A1 C17orf49 RNASEK-C17orf49 GPS2 LOC107983988 TNFSF12 TNK1 MIR497HG ALOX12 BCL6B SLC16A13 ATP1B2 SENP3 CHRNB1 TMEM102 TNFSF12-TNFSF13 TMEM256 TNFSF13 NLGN2 SNORA67 MIR195 TMEM256-PLSCR3 ACAP1 ALOX12-AS1 SLC16A11 ASGR1 MIR497 DVL2 ASGR2 LOC100996842 C17orf74 MPDU1 FXR2 SOX15 FBXO39 SNORA48 KCTD11 CD68 PLSCR3 SNORD10 CLEC10A GABARAP NEURL4 SLC2A4 SAT2 CLDN7 RNASEK MIR324 CTDNEP1 PHF23 TEKT1 SLC35G6 ACADVL EIF4A1 SHBG YBX2 ALOX12P2 TMEM95 FGF11
nsv523672 Chr.17:7379825 - 7549660 on Build GRCh38 Loss CHRNB1 POLR2A C17orf74 SPEM1 ZBTB4 TMEM102 PLSCR3 TNFSF12-TNFSF13 TMEM256 SLC35G6 NLGN2 TMEM256-PLSCR3 LOC107983988 TNFSF12 TNK1 FGF11
nsv952118 Chr.17:7174582 - 7456981 on Build GRCh38 Deletion ELP5 DLG4 C17orf74 SPEM1 EIF5A KCTD11 PLSCR3 GABARAP NEURL4 SLC2A4 GPS2 LOC107983988 CLDN7 TNK1 MIR324 CHRNB1 TMEM102 CTDNEP1 PHF23 TMEM256 NLGN2 ACADVL TMEM256-PLSCR3 ACAP1 YBX2 TMEM95 FGF11 ASGR1 DVL2
nsv574322 Chr.17:7010333 - 7689462 on Build GRCh38 Loss ELP5 DLG4 POLR2A SPEM1 ZBTB4 EIF5A TP53 SENP3-EIF4A1 C17orf49 RNASEK-C17orf49 GPS2 LOC107983988 TNFSF12 TNK1 MIR497HG ALOX12 BCL6B SLC16A13 ATP1B2 SENP3 CHRNB1 TMEM102 TNFSF12-TNFSF13 TMEM256 TNFSF13 NLGN2 SNORA67 MIR195 TMEM256-PLSCR3 ACAP1 ALOX12-AS1 SLC16A11 ASGR1 MIR497 DVL2 ASGR2 LOC100996842 C17orf74 MPDU1 FXR2 SOX15 WRAP53 SNORA48 KCTD11 CD68 PLSCR3 SNORD10 CLEC10A GABARAP NEURL4 SLC2A4 SAT2 CLDN7 RNASEK MIR324 CTDNEP1 PHF23 SLC35G6 ACADVL EIF4A1 SHBG YBX2 TMEM95 FGF11

Back To Top

More Information


Additional Information:

For this assay, SNP(s) [rs549061953] 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:

Molecular Function -

ligand-gated ion channel

Gene Ontology Categories:

Function(s) Process(es)


Back To Top

Related Products