- databases for immunodeficiency-causing variations
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NCF2base
Variation registry for Autosomal recessive p67
phox
deficiency
Select database by name
ADAbase
AICDAbase
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AK2base
AP3B1base
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CD55base
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CFIbase
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DCLRE1Cbase
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DNMT3Bbase
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FOXN1base
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G6PC3base
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HAX1base
ICOSbase
IFNGR1base
IFNGR2base
IGHG2base
IGHMbase
IGLL1base
IKBKGbase
IL12Bbase
IL12RB1base
IL2RAbase
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IRAK4base
ITGB2base
JAK3base
LIG1base
LIG4base
LRRC8Abase
LYSTbase
MAPBPIPbase
MASP2base
MLPHbase
MPObase
MRE11Abase
MYO5Abase
NCF1base
NCF2base
NFKBIAbase
NHEJ1base
NPbase
NRASbase
ORAI1base
PRF1base
PRKDCbase
PTPRCbase
RAB27Abase
RAC2base
RAD50base
RAG1base
RAG2base
RASGRP2base
RFX5base
RFXANKbase
RFXAPbase
RNF168base
SBDSbase
SERPING1base
SH2D1Abase
SLC35C1base
SMARCAL1base
SP110base
SPINK5base
STAT1base
STAT2base
STAT3base
STAT5Bbase
STIM1base
STX11base
STXBP2base
TAP1base
TAP2base
TAPBPbase
TAZbase
TCN2base
TLR3base
TMC6base
TMC8base
TNFRSF13Bbase
TYK2base
UNC13Dbase
UNC93B1base
UNGbase
WASbase
ZAP70base
NCF2base mutation types
NCF2base mutation types
The number of analyzed patients
Total
0
The number of unrelated patients
Total
0
This site is updated by
Gerard Schaafsma
© Protein Structure and Bioinformatics, Lund University, 2017
Last modified 02.03.2025
