Genomic Map
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Target Gene Details
Entrez Gene ID: | 4909 |
Gene Name: | neurotrophin 4 |
Gene Aliases: |
GLC10, GLC1O, NT-4, NT-4/5, NT-5, NT4, NT5, NTF5 |
Location: |
Chr.19:49058284-49065076 on Build GRCh38 |
Assay Gene Location: |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| NTF4 | AK297906.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv833859 | Chr.19:48997009 - 49173266 on Build GRCh38 | Loss |
 KCNA7
LIN7B
TRPM4
NTF4
PPFIA3
C19orf73
CGB8
CGB5
SNRNP70
HRC
CGB1
CGB7
LHB
RUVBL2
CGB3
SNAR-G2
SNAR-G1
CGB2
LOC101059948
MIR6798
|
| nsv9739 | Chr.19:47901840 - 50143063 on Build GRCh38 | Gain+Loss |
KCNA7
LOC100287477
SNAR-C3
SNAR-A11
HSD17B14
PLA2G4C
SULT2B1
SNAR-A7
SNAR-A14
MED25
SNAR-C2
SNORD35A
SNAR-C1
PTH2
PRRG2
ZNF473
MIR6798
SNAR-B1
CABP5
LIG1
PTOV1-AS1
CYTH2
BCAT2
SNRNP70
DHDH
C19orf68
SIGLEC16
CARD8-AS1
MIR4750
TMEM143
SEC1P
BSPH1
MIR4751
FLJ26850
TBC1D17
SNAR-A10
FTL
TRPM4
PRMT1
CGB5
IL4I1
RRAS
CGB7
LHB
CD37
VRK3
ALDH16A1
FUT1
NUCB1-AS1
PRR12
NUP62
SNAR-G1
SNORD32A
NTN5
SNAR-C5
PLEKHA4
CCDC114
NUCB1
DKKL1
SNAR-A3
CGB8
PNKP
CGB1
SNAR-A2
EMP3
CCDC155
SNAR-A13
PPP1R15A
PTOV1-AS2
SNAR-A6
CGB2
SNAR-A5
SIGLEC11
GRWD1
ELSPBP1
PIH1D1
SNAR-B2
BCL2L12
DBP
PTOV1
KDELR1
IRF3
BAX
SNORD35B
LOC105372430
LOC101059948
SNAR-A1
ADM5
FUT2
SNORD33
GRIN2D
MAMSTR
ATF5
SNAR-A9
NTF4
PPFIA3
SNAR-A8
ZNF114
FGF21
LMTK3
CGB3
SLC17A7
MIR4324
PLA2G4C-AS1
RPL18
MIR6800
SYNGR4
TULP2
SCAF1
SPHK2
SPACA4
RPL13A
TEAD2
AP2A1
MIR6799
LOC101928295
FUZ
SNAR-C4
IZUMO1
LOC105447645
GFY
C19orf73
CA11
MIR150
HRC
RCN3
FAM83E
SNAR-A4
NOSIP
RUVBL2
RPS11
SNAR-D
MIR5088
SNAR-G2
KCNJ14
SNORD34
LIN7B
SNAR-A12
AKT1S1
TSKS
CPT1C
GYS1
RASIP1
FLT3LG
MIR4749
CARD8
FCGRT
SLC6A16
|
| nsv978832 | Chr.19:49033751 - 49059401 on Build GRCh38 | Duplication |
NTF4
SNAR-G1
CGB8
CGB5
CGB1
CGB7
|
| nsv520785 | Chr.19:49050875 - 49070181 on Build GRCh38 | Gain |
KCNA7
NTF4
CGB7
|
| nsv833857 | Chr.19:48914476 - 49146320 on Build GRCh38 | Loss |
KCNA7
LIN7B
FTL
NTF4
PPFIA3
C19orf73
GYS1
CGB8
CGB5
SNRNP70
DHDH
CGB1
CGB7
LHB
RUVBL2
CGB3
NUCB1-AS1
SNAR-G2
BAX
SNAR-G1
CGB2
LOC101059948
MIR6798
NUCB1
|
| nsv953598 | Chr.19:48957644 - 49085143 on Build GRCh38 | Deletion |
KCNA7
FTL
NTF4
GYS1
CGB8
CGB5
SNRNP70
CGB1
CGB7
LHB
RUVBL2
CGB3
SNAR-G2
BAX
SNAR-G1
CGB2
LOC101059948
MIR6798
|
| esv3644612 | Chr.19:49053145 - 49063396 on Build GRCh38 | Gain |
NTF4
CGB7
|
Back To TopMore Information
Additional Information:
For this assay, SNP(s) [rs76142608] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic
Non-exonic
DGV Variation
|
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