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: | Within Intron 2 |
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_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 | MIR3187 FGF22 MIR4745 FSTL3 LOC101928450 PALM AZU1 PLPPR3 PRTN3 ELANE MED16 CFD HCN2 ARID3A KISS1R POLRMT RNU6-9 R3HDM4 PRSS57 MISP PTBP1 RNF126 |
nsv577978 | Chr.19:294526 - 782854 on Build GRCh38 | Gain | FGF22 MADCAM1 C2CD4C THEG FSTL3 CDC34 LOC101928450 PALM GZMM SHC2 MIER2 BSG HCN2 ODF3L2 TPGS1 LOC101929060 POLRMT PRSS57 MISP RNF126 |
nsv953938 | Chr.19:355801 - 1104501 on Build GRCh38 | Deletion | MIR3187 MADCAM1 GPX4 THEG MIR4745 ABCA7 FSTL3 CDC34 GRIN3B CNN2 PALM GZMM PLPPR3 ELANE MED16 CFD BSG ARID3A RNU6-2 TPGS1 RNU6-9 LOC105372235 RNF126 FGF22 C2CD4C LOC101928450 TMEM259 AZU1 PRTN3 SHC2 HCN2 ODF3L2 ARHGAP45 KISS1R POLRMT R3HDM4 WDR18 PRSS57 POLR2E MISP PTBP1 |
nsv470101 | Chr.19:401714 - 1008505 on Build GRCh38 | Loss | MIR3187 MADCAM1 MIR4745 FSTL3 CDC34 GRIN3B PALM GZMM PLPPR3 ELANE MED16 CFD BSG ARID3A TPGS1 RNU6-9 LOC105372235 RNF126 FGF22 C2CD4C LOC101928450 AZU1 PRTN3 SHC2 HCN2 ODF3L2 KISS1R POLRMT R3HDM4 WDR18 PRSS57 MISP PTBP1 |
esv3643362 | Chr.19:712133 - 716174 on Build GRCh38 | Loss | PALM |
More Information
Set Membership: |
Intragenic Intronic Non-exonic DGV Variation |