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