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