Genomic Map
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Target Gene Details
Entrez Gene ID: | 54795 |
Gene Name: | transient receptor potential cation channel subfamily M member 4 |
Gene Aliases: |
LTrpC4, PFHB1B, TRPM4B, hTRPM4 |
Location: |
Chr.19:49157741-49211841 on Build GRCh38 |
Assay Gene Location: | Within Intron 9 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| TRPM4 | NM_001195227.1 | NP_001182156.1 | ||
| NM_001321281.1 | NP_001308210.1 | |||
| NM_001321282.1 | NP_001308211.1 | |||
| NM_001321283.1 | NP_001308212.1 | |||
| NM_001321285.1 | NP_001308214.1 | |||
| NM_017636.3 | NP_060106.2 | |||
| XM_005259017.1 | XP_005259074.1 | |||
| AF497623.1 | AAM18083.1 | |||
| AJ575813.1 | CAE05941.1 | |||
| AK000048.1 | BAA90907.1 | |||
| AK292862.1 | ||||
| AK295820.1 | ||||
| AK307897.1 | ||||
| AY046396.1 | AAL02142.1 | |||
| AY297044.1 | AAP44473.1 | |||
| AY297045.1 | AAP44474.1 | |||
| AY297046.1 | AAP44475.1 | |||
| BC132727.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv9739 | Chr.19:47901840 - 50143063 on Build GRCh38 | Gain+Loss |
 PTOV1
LOC101059948
SNAR-G1
SNAR-A13
FUT1
LOC105372430
FCGRT
MIR4750
SNRNP70
PTOV1-AS2
SNAR-C2
NOSIP
SNAR-C5
SNAR-A6
GRWD1
TBC1D17
CGB1
TEAD2
PRMT1
LOC105447645
SIGLEC16
MIR4751
AP2A1
IRF3
CARD8-AS1
CA11
ATF5
PNKP
FUT2
MIR6800
ALDH16A1
NTF4
ELSPBP1
CPT1C
DBP
FGF21
PPP1R15A
CCDC114
RPL13A
FLT3LG
SEC1P
TULP2
PRRG2
SLC17A7
SULT2B1
MIR6799
EMP3
SNORD35A
CYTH2
LOC100287477
SNAR-A12
SNAR-A1
CCDC155
CGB7
FAM83E
MIR4324
TRPM4
RRAS
SNAR-A3
IZUMO1
RPS11
NTN5
VRK3
DHDH
SNORD34
SNAR-A14
SNAR-C1
LMTK3
PLEKHA4
SNAR-A9
MIR4749
FLJ26850
PLA2G4C-AS1
CGB8
SNAR-A10
GYS1
PIH1D1
RUVBL2
KCNJ14
SNAR-D
SNORD35B
HRC
SIGLEC11
CABP5
SNAR-A5
TSKS
BAX
TMEM143
BSPH1
BCL2L12
SNAR-A11
MIR5088
SYNGR4
FTL
RASIP1
C19orf68
GRIN2D
MAMSTR
NUCB1-AS1
SNAR-A8
C19orf73
IL4I1
SPACA4
MIR150
LIG1
SCAF1
PTOV1-AS1
SNAR-A2
SNAR-C3
NUCB1
LOC101928295
PTH2
LIN7B
RPL18
SNAR-B1
CGB2
NUP62
KDELR1
ADM5
AKT1S1
SPHK2
CD37
BCAT2
SNORD33
SNAR-A7
PPFIA3
HSD17B14
RCN3
MED25
PRR12
DKKL1
SNAR-B2
SNAR-G2
ZNF473
MIR6798
SNAR-A4
SLC6A16
CARD8
KCNA7
LHB
GFY
CGB3
SNAR-C4
SNORD32A
PLA2G4C
CGB5
ZNF114
FUZ
|
| dgv1057e212 | Chr.19:49165806 - 49183334 on Build GRCh38 | Loss |
TRPM4
|
| nsv1060108 | Chr.19:49118098 - 49183334 on Build GRCh38 | Gain |
LIN7B
TRPM4
HRC
C19orf73
PPFIA3
|
| dgv667e214 | Chr.19:49130606 - 49174364 on Build GRCh38 | Gain |
TRPM4
HRC
PPFIA3
|
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Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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