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