PLCG1
(
NM_002660.3
)
sequence variants
(IDAA, PLC1, NCKAP3, PLC-II, PLC148, PLCgamma1)
Editor(s):
Qing ZHOU
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A to H
genes
ADA2
ADAM17
ALPK1
AP1S3
CARD14
CDC42
CEBPE
COPA
ELF4
F12
HCK
I to L
genes
IKBKG
IL1R1
IL1RN
IL36RN
LACC1
LPIN2
LYN
M to O
genes
MEFV
MVK
NCSTN
NLRC4
NLRP1
NLRP12
NLRP3
NLRP7
NOD2
OTULIN
P to Q
genes
PLCG1
PLCG2
POMP
PSMA3
PSMB10
PSMB4
PSMB8
PSMB9
PSMG2
PSTPIP1
R to S
genes
RBCK1
RELA
RIPK1
SAMD9L
SH3BP2
SLC29A3
STING1
T to Z
genes
TNFAIP3
TNFRSF11A
TNFRSF1A
TRAP1
TRNT1
UBA1
WDR1
Close
A to H genes
ADA2
ADAM17
ALPK1
AP1S3
CARD14
CDC42
CEBPE
COPA
ELF4
F12
HCK
I to L genes
IKBKG
IL1R1
IL1RN
IL36RN
LACC1
LPIN2
LYN
M to O genes
MEFV
MVK
NCSTN
NLRC4
NLRP1
NLRP12
NLRP3
NLRP7
NOD2
OTULIN
P to Q genes
PLCG1
PLCG2
POMP
PSMA3
PSMB10
PSMB4
PSMB8
PSMB9
PSMG2
PSTPIP1
R to S genes
RBCK1
RELA
RIPK1
SAMD9L
SH3BP2
SLC29A3
STING1
T to Z genes
TNFAIP3
TNFRSF11A
TNFRSF1A
TRAP1
TRNT1
UBA1
WDR1
General web sites
DNA
NC_000020.11
GRCh38.p13
ENSG00000124181
GRCh38.p13
NC_000020.10
GRCh37.p13
ENSG00000124181
GRCh37.p13
mRNA
NM_002660.3
ENST00000685551.1
CCDS
CCDS13313.1
Protein
NP_002651.2
ENSP00000508698.1
NCBI Gene
5335
OMIM Gene
172420
OMIM Disease
620514
Nomenclature
HGNC
PubMed of the initial paper:
A gain-of-function variation in PLCG1 causes a new immune dysregulation disease
P Tao & al
Other links
:
MAP VIEW