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 Exon 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 | 1 | 174 | XP_005259622.1 | |
| XM_017026850.1 | 1 | 197 | 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 |
 MIR4745
MISP
RNU6-9
RNF126
POLRMT
PRTN3
ARID3A
HCN2
PLPPR3
R3HDM4
FGF22
KISS1R
CFD
ELANE
LOC101928450
PALM
PTBP1
AZU1
MED16
PRSS57
FSTL3
MIR3187
|
| nsv577978 | Chr.19:294526 - 782854 on Build GRCh38 | Gain |
MISP
SHC2
C2CD4C
THEG
RNF126
POLRMT
LOC101929060
HCN2
TPGS1
MADCAM1
FGF22
BSG
LOC101928450
PALM
CDC34
GZMM
PRSS57
FSTL3
MIER2
ODF3L2
|
| nsv953938 | Chr.19:355801 - 1104501 on Build GRCh38 | Deletion |
CNN2
ABCA7
MISP
SHC2
THEG
PLPPR3
MADCAM1
FGF22
KISS1R
CFD
ELANE
GRIN3B
PALM
AZU1
CDC34
MED16
PRSS57
POLR2E
FSTL3
TMEM259
MIR3187
ODF3L2
MIR4745
C2CD4C
RNU6-9
RNF126
POLRMT
PRTN3
GPX4
RNU6-2
ARID3A
HCN2
TPGS1
R3HDM4
BSG
WDR18
LOC101928450
ARHGAP45
PTBP1
LOC105372235
GZMM
|
| nsv470101 | Chr.19:401714 - 1008505 on Build GRCh38 | Loss |
MISP
SHC2
PLPPR3
MADCAM1
FGF22
KISS1R
CFD
ELANE
GRIN3B
PALM
AZU1
CDC34
MED16
PRSS57
FSTL3
MIR3187
ODF3L2
MIR4745
C2CD4C
RNU6-9
RNF126
POLRMT
PRTN3
ARID3A
HCN2
TPGS1
R3HDM4
BSG
WDR18
LOC101928450
PTBP1
LOC105372235
GZMM
|
Back To TopMore Information
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Gene Ontology Categories:
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