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