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 PALM CNV Assays ›
Gene Symbol
PALM
Assay Reference Genome
Location

Chr.19:719658 on build GRCh38
Cytoband
19p13.3
Assay ID Hs04029794_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

Assay Details

Target Gene Details

Entrez Gene ID:

 5064

Gene Name:

 paralemmin

Gene Aliases:

 -

Location:

 Chr.19:708953-748330 on Build GRCh38

Assay Gene Location:

 Overlaps Exon 3 - Intron 3
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
PALM NM_001040134.1 NP_001035224.1
NM_002579.2 NP_002570.2
XM_005259565.4 XP_005259622.1
XM_005259566.4 XP_005259623.1
XM_017026850.1 XP_016882339.1
AK299809.1
AK315168.1
BC032449.1 AAH32449.1
DA521203.1
Y14770.1 CAB37400.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
dgv134n111 Chr.19:607984 - 967584 on Build GRCh38 Deletion HCN2 FSTL3 PRSS57 PALM ARID3A FGF22 POLRMT MIR3187 PLPPR3 PRTN3 RNU6-9 KISS1R MED16 RNF126 AZU1 MISP PTBP1 CFD MIR4745 LOC101928450 ELANE R3HDM4
nsv577978 Chr.19:294526 - 782854 on Build GRCh38 Gain BSG HCN2 C2CD4C MIER2 CDC34 FSTL3 PRSS57 PALM GZMM MADCAM1 FGF22 SHC2 POLRMT ODF3L2 RNF126 MISP TPGS1 LOC101928450 THEG LOC101929060
nsv953938 Chr.19:355801 - 1104501 on Build GRCh38 Deletion LOC105372235 C2CD4C CDC34 FSTL3 PALM MADCAM1 FGF22 POLRMT MIR3187 TMEM259 PRTN3 RNU6-9 KISS1R MED16 AZU1 MISP TPGS1 MIR4745 THEG CNN2 BSG HCN2 ABCA7 PRSS57 GZMM WDR18 ARID3A SHC2 ODF3L2 PLPPR3 RNF126 ARHGAP45 GPX4 PTBP1 CFD LOC101928450 ELANE RNU6-2 R3HDM4 POLR2E GRIN3B
nsv470101 Chr.19:401714 - 1008505 on Build GRCh38 Loss LOC105372235 C2CD4C CDC34 FSTL3 PALM MADCAM1 FGF22 POLRMT MIR3187 PRTN3 RNU6-9 KISS1R MED16 AZU1 MISP TPGS1 MIR4745 BSG HCN2 PRSS57 GZMM WDR18 ARID3A SHC2 ODF3L2 PLPPR3 RNF126 PTBP1 CFD LOC101928450 ELANE R3HDM4 GRIN3B

Back To Top

More Information


Additional Information:

For this assay, SNP(s) [rs117757692] 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 Non-exonic DGV Variation

Gene Ontology Categories:

Function(s) Process(es)


Back To Top

Related Products