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