Predicted candidates
Network data for the candidate proteins in Supplementary Table 2.

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MIM #Best ScoreTitle
105550 0.435 Amyotrophic Sclerosis
108725 0.363 Atherosclerosis susceptibility
113721 0.563 Breast cancer
114400 0.274 Lynch cancer family syndrome II
125852 1.000 Diabetes mellitus, iddm2
128200 0.302 Paroxysmal kinesigenic choreoathetosis, familial
131400 0.686 Eosinophilia, familial
131440 0.496 Myeloproliferative disorder
135100 0.365 Fibrodysplasia ossificans progressiva
147061 1.000 Immunoglobulin E concentration, serum
156240 0.521 Mesothelioma, malignant
158900 1.000 Muscular dystrophy
182280 0.409 Small cell cancer of the lung
189800 0.261 Preeclampsia
191181 0.237 Cervical carcinoma
211410 0.965 Breast cancer, ductal
214300 0.355 Klippel-feil malformation
221820 0.467 Gliosis, familial progressive subcortical
236680 0.371 Hydrolethalus syndrome
273300 0.319 Testicular tumors, testicular germ cell tumor included
278250 0.678 Wrinkly skin syndrome
300030 0.239 Deafness, X-linked 4
300047 0.294 Mental retardation, x-linked 20
300076 0.307 Immunoneurologic disorder, x-linked
300238 0.292 Mental retardation, x-linked, syndromic 11
300505 0.866 Mental retardation, x-linked 84
307700 0.539 Hypoparathyroidism
313350 0.287 Split-hand/foot malformation 2
314250 0.395 Dystonia
600048 0.985 Breast cancer
600273 0.818 Polycystic kidney disease
600319 0.732 Diabetes mellitus, insulin-dependent, 4
600807 0.546 Asthma, susceptibility to
601188 0.903 Suppression of tumorigenicity 12
601286 1.000 Cataract, nonnuclear polymorphic, congenital
601363 0.296 Wilms tumor 4
601407 1.000 Type 2 diabetes
601412 0.372 Deafness, nonsyndromic sensorineural 7
601493 0.438 cardiomyopathy, dilated, 1c
601551 0.341 Blood group, Froese
601764 0.268 Convulsions, benign infantile
601869 0.630 deafness, autosomal recessive 15
602011 1.000 Pancreatic endocrine tumor
602085 1.000 Polydactyly, type a2
602096 0.778 Alzheimer disease
602221 1.000 Myeloproliferative disorder / non Hodgkin lymphoma
602404 0.228 Parkinson disease 3
602439 0.884 Acute myelogenous leukemia
602594 0.654 Retinitis pigmentosa
603045 0.437 Loss of heterozygosity, 18, chromosomal region 1
603176 0.615 Schizophrenia 7
603206 0.880 Schizophrenia 8
603388 0.891 Graves' Disease
603511 0.903 Muscular dystrophy, limb-girdle, type 1d
603664 0.933 Mental health wellness 2
603694 0.987 Diabetes mellitus, NIDDM3
604360 0.638 Spastic paraplegia 11, autosomal recessive
604401 0.645 Cardiomyopathy 6
604519 0.998 Inflammatory bowel disease 3
604805 0.409 Spastic Paraplegia
605244 0.588 Carney complex
605387 0.200 Cataract
605598 0.558 Diabetes mellitus, insulin-dependent, 18
605749 0.492 Cataract, autosomal recessive, early-onset, pulverulent
606068 0.523 Retinitis Pigmentosa
606263 0.300 Paget disease of bone 4
606482 0.924 Charcot-Marie-Tooth disease
606545 0.536 Ichthyosis
606661 0.319 Melanoma, uveal, susceptibility to, 2
606787 0.532 Peripheral arterial occlusive disease 1
607034 0.336 Fibrosis of muscles 3A
607085 0.878 Myasthenia gravis with thymus hyperplasia
607088 0.827 Spinal muscular atrophy
607116 0.644 Alzheimer disease 8
607215 0.426 Nephronophthisis-4
607279 0.815 Systemic lupus erythematosus with hemolytic anemia, 1
607339 0.237 Coronary heart disease, susceptibility to, 1
607346 0.313 Spinocerebellar ataxia 19
607398 0.930 Glucocorticoid deficiency 2
607893 0.998 Ovarian cancer, epithelial
608030 0.371 Amyotrophic Lateral Sclerosis 6
608036 0.232 Diabetes mellitus, noninsulin-dependent, 4
608088 0.382 Neuropathy, hereditary sensory, type I
608372 0.888 Deafness, sensorineural 49
608423 0.290 Muscular dystrophy, limb-girdle, type 1f
608583 0.483 Atrial fibrillation, familial, 2
608591 0.425 Charcot-Marie-Tooth disease
608691 0.597 Major depressive disorder 2
608710 0.265 Wegener granulomatosis
608816 0.397 myoclonic epilepsy, juvenile, 3
609148 1.000 Malaria, susceptibility to

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