Combined B and T cell immunodeficiencies |
T-B- Severe combined immunodeficiency (SCID) |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
Reticular dysgenesis |
|
|
|
|
|
1 |
RAG1 deficiency |
RAG1 |
|
EMBL: M29474 |
SWISSPROT: P15918 |
|
2 |
RAG2 deficiency |
RAG2 |
EMBL: M94633 |
EMBL: M94633 |
SWISSPROT: P55895 |
|
3 |
Omenn syndrome |
RAG1 |
|
EMBL: M29474, EMBL: M94633
|
SWISSPROT: P15918, SWISSPROT: P55895
|
|
4 |
Artemis deficiency |
DCLRE1C |
EMBL: AJ296101 |
EMBL: AJ296101 |
SWISSPROT: Q96SD1 |
|
5 |
T-B+ SCID |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
X-linked SCID(γc-chain deficiency) |
IL2RG |
EMBL: L19546 |
EMBL: D11086 |
SWISSPROT: P31785 |
Others |
8 |
JAK3 deficiency |
JAK3 |
EMBL: U70065 |
EMBL: U31601 |
SWISSPROT: P52333 |
Others |
9 |
Interleukin 7 receptor deficiency |
IL7R |
EMBL: M29696, EMBL: AF043129
|
EMBL: X58957 |
SWISSPROT: P16871 |
Others |
106 |
CD45 deficiency |
PTPRC |
IDRefSeq: PTPRC_DNA |
EMBL: Y00638 |
SWISSPROT: P08575 |
|
6 |
CD3delta deficiency |
CD3D |
EMBL: X03934, EMBL: M12727, EMBL: X01451
|
EMBL: X58957 |
SWISSPROT: P04234 |
Others |
111 |
T-cell immunodeficiency, congenital alopecia, and nail dystrophy |
FOXN1 |
EMBL: Y11741, EMBL: Y11739
|
EMBL: X58957 |
SWISSPROT: O15353 |
Others |
128 |
Deficiencies of purine metabolism |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
Adenosine deaminase deficiency |
ADA |
EMBL: M13792 |
EMBL: X02994 |
SWISSPROT: P00813 |
Others |
10 |
Purine nucleoside phosphorylase deficiency |
NP |
EMBL: M13953 |
EMBL: X00737 |
SWISSPROT: P00491 |
Others |
11 |
Major histocompatibility complex class II deficiency |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
CIITA, MHCII transactivating protein deficiency |
CIITA |
EMBL: X87344 |
EMBL: U18259 |
SWISSPROT: P33076 |
|
12 |
RFX-5, MHCII promoter X box regulatory factor 5 deficiency |
RFX5 |
IDRefSeq: RFX5_DNA |
EMBL: X85786 |
SWISSPROT: P48382 |
|
13 |
Regulatory factor X-associated protein deficiency |
RFXAP |
EMBL: AL159973 |
EMBL: Y12812 |
SWISSPROT: O00287 |
|
14 |
RFXANK, Ankyrin repeat containing regulatory factor X-associated protein deficiency |
RFXANK |
IDRefSeq: RFXANK_DNA |
EMBL: AF094760 |
SWISSPROT: O14593 |
Others |
15 |
Major histocompatibility complex class I deficiency |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
TAP2 deficiency |
TAP2 |
EMBL: X66401 |
EMBL: M84748 |
SWISSPROT: Q03519 |
|
60 |
TAP1 deficiency |
TAP1 |
EMBL: X66401, EMBL: X57521, EMBL: X57522, EMBL: L21204, EMBL: L21205, EMBL: L21206, EMBL: L21207, EMBL: L21208, EMBL: X87344, EMBL: S70274
|
EMBL: X58957 |
SWISSPROT: Q03518 |
|
107 |
Tapasin deficiency |
TAPBP |
EMBL: Z97183 |
EMBL: AF029750 |
SWISSPROT: O15533 |
Others |
136 |
Hyper-IgM syndrome |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
X-linked hyper-IgM syndrome (CD40L deficiency) |
TNFSF5 |
EMBL: D31793, EMBL: D31794, EMBL: D31795, EMBL: D31796, EMBL: D31797
|
EMBL: X68550 |
SWISSPROT: P29965 |
Others |
16 |
CD40 deficiency |
CD40 |
EMBL: AL035662 |
EMBL: X60592 |
SWISSPROT: P25942 |
Others |
18 |
CD3 deficiency |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
CD3ε deficiency |
CD3E |
EMBL: M23317 |
EMBL: X03884 |
SWISSPROT: P07766 |
Others |
20 |
CD3γ deficiency |
CD3G |
EMBL: M23317 |
EMBL: X04145 |
SWISSPROT: P09693 |
Others |
21 |
CD3Zeta deficiency |
CD247 |
IDRefSeq: D0115 |
EMBL: J04132 |
SWISSPROT: P20963 |
Others |
149 |
Other |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
ZAP-70 deficiency |
ZAP70 |
EMBL: AC016699 |
EMBL: L05148 |
SWISSPROT: P43403 |
|
62 |
IL-2 receptor α-chain deficiency (CD25 deficiency) |
IL2RA |
EMBL: IL2RA_DNA |
EMBL: X01057 |
SWISSPROT: P01589 |
Others |
63 |
CD8α deficiency |
CD8A |
EMBL: M27161 |
EMBL: M12828 |
SWISSPROT: P01732 |
Others |
64 |
p56 Lck deficiency |
LCK |
EMBL: X14055 |
EMBL: X13529 |
SWISSPROT: P06239 |
Others |
137 |
Schimke immuno-osseous dysplasia |
SMARCAL1 |
IDRefSeq: IDRefSeq: D0079 |
EMBL: AF082179 |
SWISSPROT: Q9NZC9 |
Others |
148 |
Cernunnos deficiency |
NHEJ1 |
IDRefSeq: D0113 |
EMBL: AJ972687 |
SWISSPROT: Q9H9Q4 |
Others |
152 |
TMEM142 deficiency |
ORAI1 |
IDRefSeq: IDRefSeq: D0114 |
EMBL: BC013386 |
SWISSPROT: Q96D31 |
Others |
147 |
Deficiencies predominantly affecting antibody production |
Agammaglobulinemia |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
X-linked agammaglobulinemia |
BTK |
EMBL: U78027 |
EMBL: X58957 |
SWISSPROT: Q06187 |
Others |
22 |
X-linked hypogammaglobulinemia with growth hormone deficiency |
|
|
|
|
|
23 |
BLNK deficiency |
BLNK |
IDRefSeq: BLNK_DNA |
EMBL: AF068180 |
SWISSPROT: O75498 |
|
24 |
Igα deficiency |
CD79A |
EMBL: U05259 |
EMBL: M86921, EMBL: X13451, EMBL: S75217, EMBL: S46706, EMBL: M80462, EMBL: X83540, EMBL: M74721
|
SWISSPROT: C79A_HUMAN |
|
25 |
μ heavy-chain deficiency |
IGHM |
EMBL: X57331 |
EMBL: X17115 |
SWISSPROT: P01871 |
Others |
26 |
λ5 surrogate light-chain deficiency |
IGLL1 |
IDRefSeq: IGLL1_DNA |
EMBL: M27749 |
SWISSPROT: P15814 |
|
27 |
Non-Bruton type autosomal dominant agammaglobulinemia |
LRRC8A |
IDRefSeq: D0055 |
EMBL: AY143166 |
SWISSPROT: Q8IWT6 |
Others |
151 |
Igβ deficiency |
CD79B |
IDRefSeq: IDRefSeq: D0126 |
EMBL: BC030210 |
SWISSPROT: Q6PIS4 |
|
159 |
Light-chain deficiency |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
κ light-chain deficiency |
IGKC |
EMBL: J00241, EMBL: V00557
|
GeneBank: AB004304 |
|
|
65 |
Selective deficiency of IgG subclass, IgE and/or IgA class or subclass |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
γ1 isotype deficiency |
IGHG1 |
GenBank: J00228 |
GenBank: AB066922 |
SWISSPROT: P01857 |
|
28 |
γ2 isotype deficiency |
IGHG2 |
GenBank: J00230 |
GenBank: AJ294731 |
SWISSPROT: P01859 |
Others |
29 |
Partial γ3 isotype deficiency |
IGHG3 |
GenBank: D78345 |
EMBL: J00231 |
SWISSPROT: P01860 |
|
30 |
γ4 isotype deficiency |
IGHG4 |
GenBank: K01316 |
GenBank: BC025985 |
SWISSPROT: P01861 |
|
31 |
α1 isotype deficiency |
IGHA1 |
EMBL: J00220 |
Genbank: AK092384 |
SWISSPROT: P01876 |
|
32 |
α2 isotype deficiency |
IGHA2 |
EMBL: J00221 |
GenBank: AL389978 |
SWISSPROT: P01877 |
|
33 |
ε isotype deficiency |
IGHE |
EMBL: L00022 |
|
SWISSPROT: P01854 |
|
34 |
IgG subclass deficiency with or without IgA deficiency |
|
|
|
|
|
35 |
IgA deficiency |
IGAD1 |
|
|
|
|
67 |
Common variable immunodeficiency |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
Common variable immunodeficiency of unknown origin |
|
|
|
|
|
66 |
ICOS deficiency |
ICOS |
EMBL: AF411058 |
GenBank: AB023135 |
SWISSPROT: Q9Y6W8 |
|
116 |
TNFRSF13B deficiency |
TNFRSF13B |
IDRefSeq: D0105 |
EMBL: AF023614 |
SWISSPROT: O14836 |
Others |
153 |
Other antibody deficiencies |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
Antibody deficiency with normal immunoglobulin levels |
|
|
|
|
|
68 |
Transient hypogammaglobulinemia of infancy |
|
|
|
|
|
69 |
CD19 deficiency |
CD19 |
IDRefSeq: CD19D |
EMBL: M21097 |
SWISSPROT: P15391 |
Others |
150 |
Defects of class-switch recombination and somatic hypermutation (Hyper-IgM syndromes) affecting B cells |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
AID deficiency |
AICDA |
EMBL: AB040430 |
EMBL: AB040431 |
TrEMBL: Q9GZX7 |
Others |
17 |
UNG deficiency |
UNG |
EMBL: X15653, EMBL: X89398, EMBL: X89398, EMBL: Y09008, EMBL: AF526277, EMBL: BC015205, EMBL: BC050634
|
EMBL: X58957 |
SWISSPROT: P13051 |
|
127 |
Selective deficiency in Ig class-switch recombination |
|
|
|
|
|
138 |
Defects in lymphocyte apoptosis |
Autoimmune lymphoproliferative syndrome |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
Autoimmune lymphoproliferative syndrome, type Ia |
TNFRSF6 |
EMBL: Z96050 |
EMBL: X89102 |
Entrez: AAC16237 |
Others |
36 |
Autoimmune lymphoproliferative syndrome, type 1B |
FASLG |
EMBL: Z96050 |
EMBL: X89102 |
SWISSPROT: P48023 |
Others |
37 |
Autoimmune lymphoproliferative syndrome type II |
CASP10 |
EMBL: U60519, EMBL: U86214, EMBL: AF111344, EMBL: AF111345, EMBL: AB038978, EMBL: AB038979
|
EMBL: X58957 |
SWISSPROT: Q92851 |
Others |
109 |
Autoimmune lymphoproliferative syndrome type IIB |
CASP8 |
EMBL: X98172, EMBL: X98173, EMBL: X98174, EMBL: X98175, EMBL: X98176, EMBL: X98177, EMBL: X98178, EMBL: U58143, EMBL: U60520, EMBL: AF102146, EMBL: AF009620, EMBL: AB038985, EMBL: AF380342, EMBL: AF422925, EMBL: AF422926, EMBL: AF422927, EMBL: AF422928, EMBL: AF422929, EMBL: BC028223
|
EMBL: X58957 |
SWISSPROT: Q14790 |
Others |
110 |
ALPS type III |
NRAS |
IDRefSeq: D0125 |
EMBL: X02751 |
SWISSPROT: P01111 |
Others |
162 |
Other well-defined immunodeficiency syndromes |
Wiskott-Aldrich syndrome and X-linked thrombocytopenia | WAS |
EMBL: AF196970 |
EMBL: U12707 |
SWISSPROT: P42768 |
Others |
71 |
Autoimmune disorders |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
Autoimmune polyendocrinopathy with candidiasis and ectodermal dystrophy |
AIRE |
EMBL: AB006684 |
EMBL: AB006682 |
SWISSPROT: O43918 |
Others |
72 |
X-linked immunodeficiency, polyendocrinopathy, enteropathy(IPEX) |
FOXP3 |
|
|
|
|
78 |
X-linked lymphoproliferative disease (Duncan disease) | SH2D1A |
EMBL: AL022718 |
EMBL: AL023657 |
SWISSPROT: O60880 |
Others |
73 |
DiGeorge-anomaly | DGCR |
|
|
|
|
74 |
Hyper-IgE recurrent infection syndrome | TYK2 |
IDRefSeq: D0118, IDRefSeq: xxx
|
EMBL: X54637, EMBL: L29277
|
SWISSPROT: P29597, SWISSPROT: P40763
|
OthersOthers
|
75 |
Chronic mucocutaneous candidiasis | |
|
|
|
|
76 |
Cartilage-hair hypoplasia | RMRP |
|
|
|
|
77 |
Epidermodysplasia verruciformis |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
Epidermodysplasia verruciformis type 1 |
TMC6 |
EMBL: BC018346 |
EMBL: X58957 |
SWISSPROT: Q7L2M4 |
|
114 |
Epidermodysplasia verruciformis type 2 |
TMC8 |
EMBL: AK090478 |
EMBL: X58957 |
SWISSPROT: Q8NF04 |
|
115 |
Netherton syndrome | SPINK5 |
EMBL: AJ228139, EMBL: AJ391230, EMBL: AF295784, EMBL: AF295783
|
EMBL: X58957 |
SWISSPROT: Q9NQ38 |
Others |
133 |
Natural killer deficiency | FCGR3A |
EMBL: X52645, EMBL: Z46222
|
EMBL: X58957 |
SWISSPROT: P08637 |
|
135 |
Transcobalamin II deficiency | TCN2 |
EMBL: M60396, EMBL: L02647, EMBL: L02648, EMBL: AF047576, EMBL: AC005006, EMBL: BC001176
|
EMBL: X58957 |
SWISSPROT: P20062 |
|
130 |
Osteopetrosis, AR | TCIRG1 |
IDRefSeq: D0101 |
EMBL: U45285 |
SWISSPROT: Q13488 |
Others |
157 |
Hepatic veno-oclussive disease with immunodeficiency syndrome | SP110 |
IDRefSeq: D0116 |
EMBL: L22342 |
GenBank: NP_536349.1 |
Others |
158 |
Tyk2 deficiency | TYK2 |
IDRefSeq: D0118 |
EMBL: X54637 |
SWISSPROT: P29597 |
Others |
163 |
X-linked lymphoproliferative syndrome 2 | BIRC4 |
IDRefSeq: D0120 |
EMBL: U45880 |
SWISSPROT: P98170 |
Others |
165 |
STAT3 deficiency | STAT3 |
IDRefSeq: D0128 |
EMBL: L29277 |
SWISSPROT: P40763 |
Others |
167 |
Defects of phagocyte function |
Chronic granulomatous disease |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
X-linked chronic granulomatous disease |
CYBB |
EMBL: X05895 |
EMBL: X04011 |
SWISSPROT: P04839 |
Others |
38 |
p22phox deficiency |
CYBA |
GenBank: M61106 |
EMBL: M21186 |
SWISSPROT: P13498 |
Others |
39 |
p47phox deficiency |
NCF1 |
EMBL: U57833 |
EMBL: M25665 |
SWISSPROT: P14598 |
Others |
40 |
p67phox deficiency |
NCF2 |
IDRefSeq: NCF2_DNA |
EMBL: M32011 |
SWISSPROT: P19878 |
Others |
41 |
Leukocyte adhesion defects |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
Leukocyte adhesion deficiency I |
ITGB2 |
EMBL: AL163300 |
EMBL: M15395 |
SWISSPROT: P05107 |
Others |
42 |
Leukocyte adhesion deficiency II |
SLC35C1 |
EMBL: IDRefSeq: SLC35C1_DNA |
EMBL: AF323970 |
SWISSPROT: Q96A29 |
Others |
43 |
LAD3 deficiency |
RASGRP2 |
IDRefSeq: D0127 |
EMBL: AF081194 |
SWISSPROT: Q7LDG7 |
Others |
139 |
LAD with RAC2 deficiency |
RAC2 |
EMBL: M29871, EMBL: AF498965, EMBL: Z82188, EMBL: BC001485, EMBL: M64595
|
EMBL: X58957 |
SWISSPROT: P15153 |
|
123 |
Chediak-Higashi syndrome | LYST |
EMBL: AL121997, EMBL: AL121997, EMBL: AL121997
|
EMBL: U84744, EMBL: U67615, EMBL: U72192, EMBL: L77889, EMBL: U70064
|
|
|
79 |
Griscelli syndrome |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
Griscelli syndrome, type 1 |
MYO5A |
EMBL: MYO5A_DNA |
EMBL: U90942, EMBL: Y07759, EMBL: Y07759, EMBL: Z22957, EMBL: S74799, EMBL: AF055459
|
UniProt/Swiss-Prot: Q9Y4I1 |
|
80 |
Griscelli syndrome, type 2 |
RAB27A |
EMBL: U38654, EMBL: U57094, EMBL: AF154840, EMBL: AF125393, EMBL: AF443871, EMBL: AF498953
|
EMBL: X58957 |
SWISSPROT: P51159 |
Others |
122 |
Griscelli syndrome, type 3 |
MLPH |
IDRefSeq: D0059 |
EMBL: AK022207 |
SWISSPROT: Q9BV36 |
Others |
156 |
Glucose 6-phosphate dehydrogenase deficiency | G6PD |
NCBI: AF277315, EMBL: L44140, EMBL: X55448, EMBL: M23423, EMBL: X53815
|
NCBI: BC000337 |
|
Others |
81 |
Myeloperoxidase deficiency | MPO |
EMBL: M17176, EMBL: X15377, EMBL: A08802
|
EMBL: M19507, EMBL: X04876, EMBL: J02694, EMBL: S56200
|
SWISSPROT: P05164 |
Others |
82 |
Glycogen storage disease Ib | G6PC |
NCBI: AF097831 |
NCBI: U01120 |
NCBI: AAD19898 |
|
83 |
Shwachman syndrome | SBDS |
IDRefSeq: SBDS_DNA |
EMBL: AY169963 |
SWISSPROT: Q9Y3A5 |
Others |
84 |
Neutropenia |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
Severe congenital neutropenias, including Kostmann syndrome |
CSF3R |
EMBL: S71484 |
EMBL: X55721, EMBL: X55720, EMBL: M59818, EMBL: M59819, EMBL: M59820
|
NCBI: AAN05790 |
|
85 |
Cyclic neutropenia |
ELA2 |
EMBL: Y00477, EMBL: M20203
|
EMBL: J03545, EMBL: X05875, EMBL: X05875, EMBL: M34379, EMBL: D00187
|
NCBI: AAS89303 |
Others |
86 |
GFI1 deficiency |
GFI1 |
EMBL: U67369, EMBL: BC032751
|
EMBL: X58957 |
SWISSPROT: Q99684 |
|
129 |
Familial haemophagocytic lymphohistiocytosis |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
Familial haemophagocytic lymphohistiocytosis type 1 |
|
|
|
|
|
104 |
Familial haemophagocytic lymphohistiocytosis type 2 |
PRF1 |
EMBL: M31951 |
EMBL: M28393 |
SWISSPROT: P14222 |
Others |
105 |
Familial hemophagocytic lymphohistiocytosis 3 |
UNC13D |
EMBL: AJ578444, EMBL: AK024474, EMBL: BC067084
|
EMBL: X58957 |
SWISSPROT: Q9H7K5 |
|
126 |
Familial haemophagocytic lymphohistiocytosis type 4 |
STX11 |
IDRefSeq: D0083 |
EMBL: AF071504 |
SWISSPROT: O75558 |
Others |
155 |
Hoyeraal-Hreidarsson syndrome/Dyskeratosis congenita | DKC1 |
EMBL: AJ224481, EMBL: U59151, EMBL: AF067008, EMBL: AF067023, EMBL: AJ010395, EMBL: BC009928, EMBL: BC010015
|
EMBL: X58957 |
SWISSPROT: O60832 |
Others |
113 |
CD64 deficiency | FCGR1A |
EMBL: X14356, EMBL: X14355, EMBL: L03418, EMBL: M91555
|
EMBL: X58957 |
SWISSPROT: P12314 |
Others |
132 |
Hermansky-Pudlak syndrome 2 | AP3B1 |
EMBL: U91931, EMBL: U81504, EMBL: BX538041, EMBL: BC038444, EMBL: AF247736
|
EMBL: X58957 |
SWISSPROT: O00203 |
|
108 |
Barth syndrome | TAZ |
EMBL: X92763, EMBL: X92762
|
EMBL: X58957 |
SWISSPROT: Q16635 |
Others |
134 |
Neutrophil-specific granule deficiency | CEBPE |
EMBL: U48865, EMBL: U48866, EMBL: U80982
|
EMBL: X58957 |
SWISSPROT: Q15744 |
|
112 |
Papillon-Lefevre syndrome | CTSC |
IDRefSeq: D0022 |
EMBL: X87212 |
SWISSPROT: P53634 |
Others |
154 |
Disorders of pigmentation and immunodeficiency |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
p14 deficiency |
MAPBPIP |
IDRefSeq: D0123 |
EMBL: C0123 |
SWISSPROT: Q9Y2Q5 |
|
161 |
Defects of innate immune system, receptors and signaling components |
Interferon-γ (IFNγ) receptor deficiency |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
IFNγ1-receptor deficiency |
IFNGR1 |
EMBL: AL050337 |
EMBL: J03143 |
SWISSPROT: P15260 |
Others |
44 |
IFNγ2-receptor deficiency |
IFNGR2 |
EMBL: AP001717 |
EMBL: U05875 |
SWISSPROT: P38484 |
Others |
45 |
Interleukin-12 receptor β1 deficiency | IL12RB1 |
IDRefSeq: IL12RB_DNA |
EMBL: U03187 |
SWISSPROT: P42701 |
Others |
47 |
Interleukin-12 (IL-12) p40 deficiency | IL12B |
EMBL: AY008847 |
EMBL: M65290 |
SWISSPROT: P29460 |
Others |
46 |
STAT1 deficiency | STAT1 |
IDRefSeq: STAT1_DNA |
EMBL: M97935 |
SWISSPROT: P42224 |
Others |
70 |
STAT5b deficiency | STAT5B |
EMBL: U48730, EMBL: U47686, EMBL: AJ412888
|
EMBL: X58957 |
SWISSPROT: P51692 |
Others |
125 |
IRAK4 deficiency | IRAK4 |
EMBL: AF445802 |
EMBL: X58957 |
SWISSPROT: Q8TDF7 |
|
117 |
Autosomal dominant anhidrotic ectodermal dysplasia and T-cell immunodeficiency | NFKBIA |
EMBL: M69043, EMBL: AJ249294, EMBL: AY033600, EMBL: BC002601, EMBL: BC004983
|
EMBL: X58957 |
SWISSPROT: P25963 |
Others |
121 |
WHIM syndrome | CXCR4 |
EMBL: AF005058 |
EMBL: NM_003467 |
SWISSPROT: P30991 |
Others |
7 |
X-linked hyper-IgM syndrome and hypohydrotic ectodermal dysplasia (Nemo deficiency) | IKBKG |
EMBL: AJ271718 |
EMBL: AF091453 |
SWISSPROT: Q9Y6K9 |
|
19 |
UNC93B deficiency | UNC93B1 |
IDRefSeq: D0122 |
EMBL: BC033623 |
SWISSPROT: Q05BS6 |
|
164 |
TLR3 deficiency | TLR3 |
IDRefSeq: D0124 |
EMBL: U88879 |
SWISSPROT: O15455 |
|
166 |
DNA breakage associated syndromes and DNA epigenetic modification syndromes |
DNA-breakage-associated syndromes |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
Ataxia-telengiectasia |
ATM |
EMBL: U82828, EMBL: U67092, EMBL: U55757, EMBL: U55757
|
EMBL: U33841, EMBL: U26455, EMBL: X91196
|
|
Others |
87 |
Nijmegen-breakage syndrome |
NBS1 |
|
|
|
|
88 |
Ataxia-telangiectasia-like disorder |
MRE11A |
EMBL: U37359, EMBL: AF022778, EMBL: AF073362, EMBL: AF303395
|
EMBL: X58957 |
SWISSPROT: P49959 |
Others |
120 |
DNA ligase deficiency |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
DNA ligase I deficiency |
LIG1 |
EMBL: M36067, EMBL: AF527418
|
EMBL: X58957 |
SWISSPROT: P18858 |
|
131 |
DNA ligase deficiency IV |
LIG4 |
EMBL: X83441, EMBL: AF479264
|
EMBL: X58957 |
SWISSPROT: P49917 |
|
118 |
Bloom syndrome | BLM |
EMBL: AC002312 |
EMBL: U39817 |
SWISSPROT: P54132 |
|
89 |
Immunodeficiency, centromere instability and facial abnormalities syndrome (ICF) | DNMT3B |
EMBL: AL035071 |
EMBL: X58957 |
SWISSPROT: Q9UBC3 |
Others |
124 |
Defects of the classical complement cascade proteins |
C1q deficiency |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
C1q α-polypeptide deficiency |
C1QA |
C1QAbase: C1QA_DNA |
EMBL: AF135157 |
SWISSPROT: P02745 |
|
48 |
C1q β-polypeptide deficiency |
C1QB |
NCBI: AL158086 |
GenBank: NM_000491 |
SWISSPROT: P02746 |
Others |
49 |
C1q γ-polypeptide deficiency |
C1QC |
NCBI: AL158086 |
EMBL: BC009016 |
SWISSPROT: P02747 |
Others |
50 |
C1r and C1s deficiency |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
C1r deficiency |
C1R |
GenBank: AB083037 |
EMBL: M14058 |
SWISSPROT: P00736 |
Others |
51 |
C1s deficiency |
C1S |
C1Sbase: C1S_DNA |
EMBL: J04080 |
SWISSPROT: P09871 |
Others |
52 |
C2 deficiency | C2 |
EMBL: AF019413 |
EMBL: X04481 |
SWISSPROT: P06681 |
Others |
90 |
C3 deficiency | C3 |
EMBL: C3_DNA |
EMBL: K02765 |
SWISSPROT: P01024 |
|
61 |
C4 deficiency |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
C4A deficiency |
C4A |
GenBank: AL929593 |
GenBank: NM_007293 |
SWISSPROT: P01028 |
Others |
53 |
C4B deficiency |
C4B |
GenBank: HSMHCT8S22 |
GenBank: NM_000592 |
SWISSPROT: P01028 |
Others |
54 |
C5 deficiency | C5 |
EMBL: AC006430 |
EMBL: M57729 |
SWISSPROT: P01031 |
Others |
91 |
C6 deficiency | C6 |
C6base: C6_DNA |
GenBank: NM_000065 |
SWISSPROT: P13671 |
Others |
92 |
C7 deficiency | C7 |
C7base: C7_DNA |
EMBL: J03507 |
SWISSPROT: P10643 |
Others |
93 |
C8 deficiency |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
C8 α-polypeptide deficiency |
C8A |
EMBL: AL121998 |
EMBL: M16974 |
SWISSPROT: P07357 |
Others |
55 |
C8 β-polypeptide deficiency |
C8B |
EMBL: AL121998 |
EMBL: M16973 |
SWISSPROT: P07358 |
Others |
56 |
C8 γ-polypeptide deficiency |
C8G |
EMBL: U08198 |
EMBL: X06465 |
SWISSPROT: P07360 |
Others |
57 |
C9 deficiency | C9 |
C9base: C9_DNA |
EMBL: X02176 |
SWISSPROT: P02748 |
Others |
94 |
Defects of the alternative complement pathway |
Factor B deficiency | BF |
GenBank: AF019413 |
GenBank: NM_001710 |
SWISSPROT: P00751 |
Others |
95 |
Factor D deficiency | CFD |
|
EMBL: M84526 |
SWISSPROT: P00746 |
|
98 |
Factor H1 deficiency | CFH |
EMBL: AL049744 |
EMBL: Y00716 |
SWISSPROT: P08603 |
Others |
101 |
Properdin factor C deficiency | CFP |
EMBL: X70872 |
GenBank: NM_002621 |
SWISSPROT: P27918 |
Others |
100 |
Defects of complement regulatory proteins |
Hereditary angioedema |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
Hereditary angioedema |
SERPING1 |
GenBank: AF435921 |
GenBank: NM_000062 |
SWISSPROT: P05155 |
Others |
97 |
C4-binding protein deficiency |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
C4 binding protein α deficiency |
C4BPA |
GenBank: AL445493 |
EMBL: BC022312 |
SWISSPROT: P04003 |
Others |
58 |
C4 binding protein β deficiency |
C4BPB |
GenBank: AL44549 |
EMBL: L11244 |
SWISSPROT: P20851 |
Others |
59 |
Hereditary angioedema type III |
F12 |
IDRefSeq: D0119 |
EMBL: M31315 |
SWISSPROT: P00748 |
Others |
160 |
Decay-accelerating factor (CD55) deficiency | CD55 |
GenBank: AB003312 |
EMBL: M31516 |
SWISSPROT: P08174 |
Others |
102 |
Factor I deficiency | CFI |
IDRefSeq: IF_DNA |
EMBL: J02770 |
SWISSPROT: P05156 |
Others |
99 |
MAC inhibitor (CD59) deficiency | CD59 |
EMBL: M84345, EMBL: M84349, EMBL: Z14113
|
EMBL: M27909, EMBL: M95708, EMBL: X16447, EMBL: X17198, EMBL: X15861, EMBL: M34671
|
SWISSPROT: P13987 |
Others |
103 |
Mannose-binding lectin deficiency |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
Mannose-binding lectin deficiency |
MBL2 |
EMBL: X15954, EMBL: AF080510, EMBL: Y16576, EMBL: Y16577, EMBL: Y16578, EMBL: Y16579, EMBL: Y16580, EMBL: Y16581, EMBL: Y16582
|
EMBL: X15422, EMBL: AF360991
|
GenPept: BAB17020 |
Others |
96 |
Mannan-binding lectin - associated serine protease 2 deficiency |
MASP2 |
EMBL: Y09926, EMBL: X98400, EMBL: Y18281, EMBL: Y18283, EMBL: Y18284, EMBL: Y18286, EMBL: Y18286, EMBL: Y18287, EMBL: Y18287, EMBL: AB008047, EMBL: AB033742, EMBL: AF321562, EMBL: AF321558
|
EMBL: X58957 |
SWISSPROT: O00187 |
Others |
119 |
Periodic fever syndromes |
Familial mediterranean fever | MEFV |
EMBL: AJ003147 |
EMBL: AF018080 |
SWISSPROT: O15553 |
Others |
140 |
Hyperimmunoglobulinemia D with periodic fever syndrome | MVK |
EMBL: AF217535 |
EMBL: M88468 |
SWISSPROT: Q03426 |
Others |
141 |
Tumor necrosis factor receptor-associated periodic syndrome | TNFRSF1A |
EMBL: M75866 |
EMBL: X55313 |
SWISSPROT: P19438 |
Others |
142 |
Cold autoinflammatory syndrome |
Disease
|
Gene |
DNA |
RNA |
Protein |
Others |
Fact file |
Familial cold urticaria and Muckle-Wells syndrome |
CIAS1 |
EMBL: AY051117 |
EMBL: AF410477 |
SWISSPROT: Q96P20 |
Others |
143 |
Chronic infantile neurological cutaneous and articular syndrome |
CIAS1 |
EMBL: AY051117 |
EMBL: AF410477 |
SWISSPROT: Q96P20 |
Others |
144 |
Granulomatous sinovitis with uveitis and cranial neuropathies | CARD15 |
EMBL: AF385089 |
EMBL: AF178930 |
SWISSPROT: Q9HC29 |
Others |
145 |
Crohn's disease | CARD15 |
EMBL: AF385089 |
EMBL: AF178930 |
SWISSPROT: Q9HC29 |
Others |
146 |