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 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 |
 FSTL3
LOC101928450
RNU6-9
ARID3A
MIR3187
PRSS57
KISS1R
RNF126
MISP
AZU1
PRTN3
HCN2
PTBP1
MED16
FGF22
POLRMT
CFD
PLPPR3
R3HDM4
MIR4745
PALM
ELANE
|
| nsv577978 | Chr.19:294526 - 782854 on Build GRCh38 | Gain |
CDC34
FSTL3
LOC101928450
LOC101929060
MADCAM1
THEG
MIER2
C2CD4C
PRSS57
BSG
TPGS1
RNF126
GZMM
MISP
HCN2
FGF22
POLRMT
SHC2
ODF3L2
PALM
|
| nsv953938 | Chr.19:355801 - 1104501 on Build GRCh38 | Deletion |
CDC34
POLR2E
LOC101928450
ARHGAP45
WDR18
MIR3187
ABCA7
BSG
TPGS1
GZMM
GRIN3B
MISP
AZU1
PRTN3
HCN2
PTBP1
MED16
POLRMT
SHC2
R3HDM4
ODF3L2
LOC105372235
FSTL3
MADCAM1
THEG
CNN2
C2CD4C
RNU6-9
ARID3A
RNU6-2
PRSS57
KISS1R
RNF126
TMEM259
FGF22
CFD
PLPPR3
MIR4745
GPX4
PALM
ELANE
|
| nsv470101 | Chr.19:401714 - 1008505 on Build GRCh38 | Loss |
CDC34
LOC101928450
WDR18
MIR3187
BSG
TPGS1
GZMM
GRIN3B
MISP
AZU1
PRTN3
HCN2
PTBP1
MED16
POLRMT
SHC2
R3HDM4
ODF3L2
LOC105372235
FSTL3
MADCAM1
C2CD4C
RNU6-9
ARID3A
PRSS57
KISS1R
RNF126
FGF22
CFD
PLPPR3
MIR4745
PALM
ELANE
|
| esv3643363 | Chr.19:712133 - 716174 on Build GRCh38 | Gain |
PALM
|
Back To TopMore Information
Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Gene Ontology Categories:
Back To Top