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 |
 CGB2
SNAR-G2
LOC101059948
LHB
HRC
SNRNP70
KCNA7
CGB8
MIR6798
NTF4
SNAR-G1
CGB3
CGB5
CGB7
PPFIA3
RUVBL2
C19orf73
LIN7B
TRPM4
CGB1
|
| nsv9739 | Chr.19:47901840 - 50143063 on Build GRCh38 | Gain+Loss |
SNAR-G2
VRK3
MIR4749
BCL2L12
SULT2B1
FLT3LG
ATF5
TMEM143
MAMSTR
SNAR-A1
RPL13A
AKT1S1
NUCB1
CPT1C
PTOV1-AS2
SNAR-A12
SLC6A16
CYTH2
LOC101059948
CCDC114
RPS11
SNAR-A14
SPACA4
BCAT2
RASIP1
NOSIP
ADM5
SNAR-C1
CARD8-AS1
AP2A1
LIG1
NUP62
BSPH1
PRR12
SNAR-A13
CCDC155
MIR6800
PLEKHA4
MIR5088
FGF21
LOC101928295
SNAR-G1
SNAR-A5
C19orf68
TBC1D17
DKKL1
SNORD34
PTH2
HSD17B14
CGB2
SNRNP70
SNAR-C2
MIR150
SNAR-A3
SEC1P
LMTK3
SLC17A7
CABP5
FUZ
GRWD1
KCNJ14
CGB1
LOC105372430
LOC105447645
RCN3
KDELR1
SNORD35B
NUCB1-AS1
EMP3
SNAR-A7
CGB3
SNAR-C4
SCAF1
C19orf73
CA11
PRRG2
TSKS
FUT2
SNAR-A9
LHB
PLA2G4C-AS1
SNAR-A4
GRIN2D
NTF4
PIH1D1
PPP1R15A
CGB5
LOC100287477
PRMT1
CGB7
SNAR-A6
GFY
RRAS
ZNF473
TRPM4
SNORD32A
RPL18
FLJ26850
FTL
TEAD2
HRC
PLA2G4C
KCNA7
CGB8
MIR4324
ALDH16A1
GYS1
SIGLEC11
TULP2
DHDH
CARD8
SNAR-A10
MIR4751
SNAR-A8
SNAR-D
IL4I1
MED25
SNORD33
PPFIA3
PNKP
SNORD35A
SIGLEC16
SNAR-A11
MIR6799
ZNF114
BAX
FUT1
IZUMO1
PTOV1
FCGRT
SNAR-B2
IRF3
CD37
MIR6798
ELSPBP1
SNAR-A2
NTN5
RUVBL2
PTOV1-AS1
DBP
FAM83E
LIN7B
SNAR-C5
SYNGR4
SNAR-C3
SNAR-B1
MIR4750
SPHK2
|
| nsv978832 | Chr.19:49033751 - 49059401 on Build GRCh38 | Duplication |
CGB7
CGB8
NTF4
SNAR-G1
CGB1
CGB5
|
| nsv833857 | Chr.19:48914476 - 49146320 on Build GRCh38 | Loss |
CGB2
SNAR-G2
LOC101059948
LHB
SNRNP70
NUCB1-AS1
KCNA7
CGB8
MIR6798
NTF4
GYS1
SNAR-G1
DHDH
CGB3
CGB5
NUCB1
CGB7
PPFIA3
RUVBL2
C19orf73
LIN7B
CGB1
BAX
FTL
|
| nsv520785 | Chr.19:49050875 - 49070181 on Build GRCh38 | Gain |
CGB7
KCNA7
NTF4
|
| nsv953598 | Chr.19:48957644 - 49085143 on Build GRCh38 | Deletion |
CGB2
SNAR-G2
LOC101059948
LHB
SNRNP70
KCNA7
CGB8
MIR6798
NTF4
GYS1
SNAR-G1
CGB3
CGB5
CGB7
RUVBL2
CGB1
BAX
FTL
|
| esv3644612 | Chr.19:49053145 - 49063396 on Build GRCh38 | Gain |
CGB7
NTF4
|
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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