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 |
 LOC101928450
MIR4745
RNF126
PALM
FSTL3
ELANE
HCN2
PTBP1
POLRMT
FGF22
MED16
R3HDM4
RNU6-9
ARID3A
PLPPR3
AZU1
MIR3187
PRSS57
CFD
MISP
PRTN3
KISS1R
|
| nsv577978 | Chr.19:294526 - 782854 on Build GRCh38 | Gain |
LOC101929060
LOC101928450
RNF126
CDC34
SHC2
PALM
BSG
ODF3L2
FSTL3
HCN2
MIER2
MADCAM1
POLRMT
FGF22
C2CD4C
PRSS57
TPGS1
MISP
THEG
GZMM
|
| nsv953938 | Chr.19:355801 - 1104501 on Build GRCh38 | Deletion |
MIR4745
SHC2
PALM
BSG
ODF3L2
ELANE
ABCA7
HCN2
GRIN3B
POLRMT
MED16
R3HDM4
RNU6-9
C2CD4C
PRSS57
POLR2E
CFD
TPGS1
WDR18
MISP
PRTN3
RNU6-2
GZMM
LOC101928450
RNF126
CDC34
FSTL3
MADCAM1
PTBP1
FGF22
ARID3A
PLPPR3
TMEM259
AZU1
MIR3187
GPX4
LOC105372235
CNN2
ARHGAP45
THEG
KISS1R
|
| nsv470101 | Chr.19:401714 - 1008505 on Build GRCh38 | Loss |
MIR4745
SHC2
PALM
BSG
ODF3L2
ELANE
HCN2
GRIN3B
POLRMT
MED16
R3HDM4
RNU6-9
C2CD4C
PRSS57
CFD
TPGS1
WDR18
MISP
PRTN3
GZMM
LOC101928450
RNF126
CDC34
FSTL3
MADCAM1
PTBP1
FGF22
ARID3A
PLPPR3
AZU1
MIR3187
LOC105372235
KISS1R
|
| esv3643362 | Chr.19:712133 - 716174 on Build GRCh38 | Loss |
PALM
|
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Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Gene Ontology Categories:
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