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 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| PALM | NM_001040134.1 | NP_001035224.1 | ||
| NM_002579.2 | NP_002570.2 | |||
| 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 |
 FGF22
RNU6-9
PALM
MIR3187
PTBP1
KISS1R
MISP
POLRMT
RNF126
MIR4745
PLPPR3
CFD
ARID3A
FSTL3
AZU1
MED16
HCN2
ELANE
PRTN3
R3HDM4
PRSS57
LOC101928450
|
| nsv577978 | Chr.19:294526 - 782854 on Build GRCh38 | Gain |
SHC2
BSG
FGF22
PALM
THEG
MIER2
C2CD4C
ODF3L2
MISP
POLRMT
RNF126
GZMM
FSTL3
MADCAM1
HCN2
LOC101929060
CDC34
PRSS57
TPGS1
LOC101928450
|
| nsv953938 | Chr.19:355801 - 1104501 on Build GRCh38 | Deletion |
BSG
ABCA7
LOC105372235
PTBP1
WDR18
MIR4745
GPX4
MED16
TPGS1
SHC2
ARHGAP45
FGF22
GRIN3B
RNU6-9
PALM
THEG
TMEM259
MIR3187
C2CD4C
ODF3L2
POLR2E
KISS1R
MISP
POLRMT
RNF126
GZMM
PLPPR3
CNN2
CFD
ARID3A
FSTL3
AZU1
MADCAM1
HCN2
ELANE
PRTN3
R3HDM4
CDC34
PRSS57
LOC101928450
RNU6-2
|
| nsv470101 | Chr.19:401714 - 1008505 on Build GRCh38 | Loss |
BSG
LOC105372235
PTBP1
WDR18
MIR4745
MED16
TPGS1
SHC2
FGF22
GRIN3B
RNU6-9
PALM
MIR3187
C2CD4C
ODF3L2
KISS1R
MISP
POLRMT
RNF126
GZMM
PLPPR3
CFD
ARID3A
FSTL3
AZU1
MADCAM1
HCN2
ELANE
PRTN3
R3HDM4
CDC34
PRSS57
LOC101928450
|
Back To TopMore Information
Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Gene Ontology Categories:
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