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