Search results for Calcineurin Autoinhibitory Peptide

195 hits were found for Calcineurin Autoinhibitory Peptide

# Family MCID Name MIFTS Score
1
HLX001 Helix Syndrome 47 26.819
2
RPD005 Rapidly Involuting Congenital Hemangioma 48 17.675
3
P ALZ034 Alzheimer Disease 87 16.117
4
CNG034 Congestive Heart Failure 69 15.414
5
P DBT009 Diabetes Mellitus 67 15.222
6
HMN044 Human Immunodeficiency Virus Type 1 76 14.617
7
PRT037 Pertussis 49 14.156
8
ATM095 Autoimmune Disease 61 13.176
9
P NRB001 Neuroblastoma 66 13.072
10
P RHM011 Rheumatoid Arthritis 81 12.851
11
CYT002 Cytokine Deficiency 43 12.813
12
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 12.401
13
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 12.294
14
P DRM053 Dermatitis, Atopic 65 12.231
15
c HYP595 Hypertension, Essential 84 11.911
16
BCT022 Bacterial Infectious Disease 55 11.904
17
PRT251 Proteinuria, Chronic Benign 58 11.617
18
GLL048 Glial Tumor 51 11.389
19
GLM045 Glioma 62 11.379
20
DWN001 Down Syndrome 70 11.369
21
IMM167 Immune Deficiency Disease 76 11.167
22
P ART022 Arthritis 70 11.076
23
c HPT073 Hepatitis C Virus 70 10.845
24
GLB002 Glioblastoma 67 10.830
25
48X005 48,xyyy 39 10.594
26
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 10.387
27
TTN003 Tetanus 64 10.334
28
DRM006 Dermatitis 61 10.154
29
P MYC007 Myocardial Infarction 69 10.089
30
P LKM002 Leukemia 65 10.034
31
ALL029 Allergic Disease 61 9.948
32
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 9.946
33
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 9.946
34
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 9.946
35
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 9.946
36
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 9.946
37
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 9.946
38
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 9.946
39
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 9.946
40
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 9.946
41
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 9.915
42
c HPT001 Hepatitis C 61 9.889
43
SKN016 Skin Disease 63 9.566
44
LNG099 Lung Disease 62 9.545
45
P NPH012 Nephrotic Syndrome 61 9.381
46
CHL014 Cholera 62 9.187
47
c LKM061 Leukemia, Acute Myeloid 83 8.978
48
INS024 Insulin-Like Growth Factor I 77 8.967
49
P MYL006 Myeloid Leukemia 60 8.956
50
HYP266 Hypoxia 56 8.880
51
INS001 Insulinoma 59 8.840
52
P BRS047 Breast Cancer 97 8.707
53
MSC007 Muscle Hypertrophy 64 8.563
54
c LKM063 Leukemia, Chronic Myeloid 70 8.462
55
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 8.185
56
P ATR011 Atrial Fibrillation 66 7.985
57
SVR004 Severe Combined Immunodeficiency 70 7.927
58
MYL009 Myelodysplastic Syndrome 67 7.893
59
P LYM118 Lymphoma 66 7.720
60
P HPT023 Hepatocellular Carcinoma 95 7.663
61
P ENC018 Encephalopathy 62 7.501
62
47X002 47,xyy 47 7.462
63
P DRR001 Diarrhea 55 7.382
64
GLC003 Glucose Intolerance 53 7.233
65
P LKM062 Leukemia, Acute Lymphoblastic 69 7.191
66
P MSC005 Muscular Dystrophy 66 7.189
67
P HNT016 Huntington Disease 73 7.177
68
MDD018 Middle East Respiratory Syndrome 44 6.990
69
P BCL017 B-Cell Lymphoma 57 6.841
70
P GST053 Gastric Cancer 82 6.830
71
P MYC084 Mycobacterium Tuberculosis 1 68 6.784
72
THY029 Thyroid Carcinoma 55 6.751
73
BRN071 Brain Injury 50 6.649
74
STM007 Stomatitis 52 6.398
75
P NRP001 Neuropathy 59 6.388
76
TRM010 Traumatic Brain Injury 50 6.356
77
CRB004 Cerebral Artery Occlusion 45 6.329
78
PPL052 Papillomatosis, Confluent and Reticulated 34 6.324
79
P RTN024 Retinoblastoma 72 5.926
80
P PRP019 Peripheral Nervous System Disease 57 5.745
81
P DNG005 Dengue Virus 55 5.702
82
ADN018 Adenoma 58 5.563
83
MLR004 Malaria 77 5.420
84
P SZR006 Seizure Disorder 69 5.185
85
c MCR115 Microvascular Complications of Diabetes 5 65 5.143
86
P DMN002 Dementia 65 5.093
87
RCK004 Rickets 64 5.014
88
DWR001 Dwarfism 44 4.920
89
P MYC008 Myocarditis 59 4.917
90
P NTR004 Neutropenia 62 4.915
91
P FBR017 Fibrosarcoma 55 4.847
92
P THY032 Thyroiditis 56 4.836
93
MYL031 Myeloproliferative Neoplasm 66 4.753
94
BRN002 Bronchiolitis 57 4.630
95
P THR014 Thrombocytopenia 66 4.630
96
DMY004 Demyelinating Disease 50 4.512
97
P MYP004 Myopathy 67 4.503
98
c CRN279 Cornea Plana 1, Autosomal Dominant 19 4.503
99
P LKM071 Leukemia, Chronic Lymphocytic 74 4.497
100
P MSC003 Muscular Atrophy 52 4.496
101
BRN028 Brain Cancer 73 4.485
102
P MDL005 Medulloblastoma 75 4.479
103
HRT012 Heart Valve Disease 53 4.367
104
P RHB003 Rhabdomyosarcoma 66 4.356
105
P LNG064 Lung Cancer Susceptibility 3 69 4.350
106
PNC129 Pancreatic Adenocarcinoma 64 4.287
107
P EXN002 Exanthem 58 4.273
108
P HYP098 Hypereosinophilic Syndrome 66 4.245
109
P AST005 Asthma 75 4.166
110
MNT002 Mental Depression 56 4.118
111
c ACT073 Acute Leukemia 59 4.032
112
MDD011 Mood Disorder 61 3.942
113
P ALP008 Alopecia 53 3.859
114
EWN003 Ewing Sarcoma 69 3.827
115
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 3.811
116
P FCL005 Focal Segmental Glomerulosclerosis 57 3.766
117
c THY107 Thymoma, Familial 42 3.657
118
P THY023 Thymoma 64 3.657
119
ACT098 Acute Erythroid Leukemia 55 3.628
120
INT323 Intraocular Pressure Quantitative Trait Locus 63 3.573
121
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 3.535
122
VRL011 Viral Infectious Disease 60 3.529
123
THR004 Thrombocytosis 52 3.341
124
P URT039 Urticaria 57 3.325
125
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 3.288
126
MYL005 Myelofibrosis 70 3.270
127
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 3.185
128
P MJR001 Major Depressive Disorder 68 3.134
129
c CRN280 Cornea Plana 2, Autosomal Recessive 25 3.093
130
HSH003 Hashimoto Thyroiditis 60 3.059
131
DFF005 Diffuse Large B-Cell Lymphoma 55 3.023
132
P PLY018 Polycythemia 56 3.005
133
ANX004 Anoxia 40 2.998
134
P CHR285 Chronic Myelomonocytic Leukemia 59 2.989
135
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 2.978
136
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 59 2.959
137
P FML011 Familial Adenomatous Polyposis 70 2.955
138
P HMP007 Hemophilia 52 2.947
139
BRN004 Brain Edema 54 2.879
140
P WSK001 Wiskott-Aldrich Syndrome 72 2.862
141
FRN006 Frontotemporal Dementia 68 2.794
142
ENT011 Enterocolitis 55 2.776
143
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 2.685
144
PMP014 Pemphigoid 48 2.572
145
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 2.503
146
BLL006 Bullous Pemphigoid 61 2.452
147
P MYT002 Myotonic Dystrophy 51 2.400
148
P ESS003 Essential Thrombocythemia 68 2.382
149
TRT001 Teratocarcinoma 41 2.327
150
PLY001 Polycythemia Vera 69 2.314
151
CRY035 Cryptorchidism, Unilateral or Bilateral 57 2.309
152
P RTN016 Retinal Degeneration 52 2.304
153
JVN004 Juvenile Myelomonocytic Leukemia 66 2.272
154
c BRN108 Branchiootic Syndrome 1 63 2.213
155
P FLL037 Follicular Lymphoma 66 2.146
156
P LMB006 Limb-Girdle Muscular Dystrophy 52 2.037
157
P SLM003 Salmonellosis 54 1.875
158
P MST009 Mastocytosis 64 1.846
159
IGR001 Ige Responsiveness, Atopic 58 1.828
160
P PRP029 Porphyria 60 1.785
161
P NRF002 Neurofibromatosis 60 1.782
162
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 1.693
163
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.678
164
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 1.607
165
CMM004 Common Variable Immunodeficiency 71 1.602
166
P SNS001 Sensorineural Hearing Loss 60 1.590
167
NRL016 Neural Tube Defects 80 1.568
168
RFR010 Refractory Anemia 49 1.500
169
P CRN037 Craniosynostosis 67 1.479
170
P SBS003 Substance Abuse 54 1.408
171
c FNC027 Fanconi Anemia, Complementation Group a 80 1.381
172
c HYP272 Hypercholesterolemia, Familial, 3 46 1.308
173
WLL004 Wallerian Degeneration 38 1.275
174
CNG506 Congenital Amyoplasia 27 1.242
175
c SVR003 Severe Congenital Neutropenia 59 1.235
176
P NNN008 Noonan Syndrome 1 76 1.212
177
c PSD047 Pseudo-Turner Syndrome 52 1.207
178
P PLY017 Polyarteritis Nodosa 59 1.045
179
HYP025 Hyperphosphatemia 47 1.035
180
HST010 Histiocytosis 49 1.016
181
PRP016 Paraplegia 52 0.968
182
CLF027 Cleft Palate, Isolated 64 0.876
183
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 44 0.864
184
MCR018 Microcytic Anemia 46 0.836
185
P PSD003 Pseudohypoaldosteronism 45 0.797
186
c THR071 Thrombocytopenia 1 48 0.772
187
LNT004 Lentigines 45 0.705
188
LNG108 Langerhans Cell Histiocytosis 57 0.683
189
RSP023 Rasopathy 54 0.665
190
LBR036 Leber Plus Disease 67 0.591
191
SYS004 Systemic Mastocytosis 62 0.556
192
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.488
193
NNN026 Noonan Syndrome with Multiple Lentigines 64 0.472
194
P CNT004 Centronuclear Myopathy 56 0.380
195
c PSD093 Pseudohypoaldosteronism, Type Iid 31 0.274
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