Genomic Map
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Target Gene Details
Entrez Gene ID: | 5064 |
Gene Name: | paralemmin |
Gene Aliases: |
- |
Location: |
Chr.19:708953-748330 on Build GRCh38 |
Assay Gene Location: | Within Exon 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 | 1 | 162 | 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 |
 RNF126
MED16
PRTN3
RNU6-9
MIR3187
MIR4745
KISS1R
HCN2
PLPPR3
CFD
POLRMT
LOC101928450
AZU1
PRSS57
MISP
FSTL3
PTBP1
PALM
ARID3A
ELANE
FGF22
R3HDM4
|
| nsv577978 | Chr.19:294526 - 782854 on Build GRCh38 | Gain |
RNF126
C2CD4C
GZMM
ODF3L2
LOC101929060
SHC2
CDC34
HCN2
TPGS1
MIER2
POLRMT
LOC101928450
PRSS57
MISP
FSTL3
MADCAM1
PALM
FGF22
THEG
BSG
|
| nsv953938 | Chr.19:355801 - 1104501 on Build GRCh38 | Deletion |
GZMM
PRTN3
ODF3L2
MIR3187
POLR2E
GPX4
CDC34
PLPPR3
ARHGAP45
CFD
TPGS1
RNU6-2
AZU1
PRSS57
MADCAM1
PTBP1
PALM
ELANE
WDR18
FGF22
THEG
BSG
R3HDM4
LOC105372235
RNF126
C2CD4C
MED16
TMEM259
RNU6-9
SHC2
GRIN3B
MIR4745
KISS1R
HCN2
POLRMT
LOC101928450
CNN2
MISP
FSTL3
ARID3A
ABCA7
|
| nsv470101 | Chr.19:401714 - 1008505 on Build GRCh38 | Loss |
GZMM
PRTN3
ODF3L2
MIR3187
CDC34
PLPPR3
CFD
TPGS1
AZU1
PRSS57
MADCAM1
PTBP1
PALM
ELANE
WDR18
FGF22
BSG
R3HDM4
LOC105372235
RNF126
C2CD4C
MED16
RNU6-9
SHC2
GRIN3B
MIR4745
KISS1R
HCN2
POLRMT
LOC101928450
MISP
FSTL3
ARID3A
|
Back To TopMore Information
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Gene Ontology Categories:
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