Genomic Map
Back To TopAssay 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 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| PALM | NM_001040134.1 | NP_001035224.1 | ||
| NM_002579.2 | NP_002570.2 | |||
| 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 |
 MIR4745
AZU1
PALM
FSTL3
RNF126
ELANE
PRTN3
MIR3187
MISP
MED16
PLPPR3
CFD
LOC101928450
PRSS57
RNU6-9
PTBP1
FGF22
POLRMT
KISS1R
HCN2
ARID3A
R3HDM4
|
| nsv577978 | Chr.19:294526 - 782854 on Build GRCh38 | Gain |
CDC34
THEG
TPGS1
GZMM
PALM
MIER2
C2CD4C
FSTL3
RNF126
SHC2
MISP
LOC101929060
MADCAM1
LOC101928450
BSG
PRSS57
ODF3L2
FGF22
POLRMT
HCN2
|
| nsv953938 | Chr.19:355801 - 1104501 on Build GRCh38 | Deletion |
MIR4745
CDC34
THEG
GZMM
PALM
WDR18
C2CD4C
LOC105372235
MIR3187
LOC101928450
PRSS57
POLR2E
PTBP1
ABCA7
ARHGAP45
FGF22
POLRMT
GPX4
HCN2
RNU6-2
R3HDM4
TPGS1
AZU1
FSTL3
RNF126
ELANE
PRTN3
TMEM259
SHC2
MISP
MED16
PLPPR3
MADCAM1
CFD
BSG
GRIN3B
RNU6-9
ODF3L2
KISS1R
CNN2
ARID3A
|
| nsv470101 | Chr.19:401714 - 1008505 on Build GRCh38 | Loss |
MIR4745
CDC34
GZMM
PALM
WDR18
C2CD4C
LOC105372235
MIR3187
LOC101928450
PRSS57
PTBP1
FGF22
POLRMT
HCN2
R3HDM4
TPGS1
AZU1
FSTL3
RNF126
ELANE
PRTN3
SHC2
MISP
MED16
PLPPR3
MADCAM1
CFD
BSG
GRIN3B
RNU6-9
ODF3L2
KISS1R
ARID3A
|
Back To TopMore Information
Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Gene Ontology Categories:
Back To Top