| Disease |
Protein |
BMRB entry |
| 3-M syndrome |
Obscurin-like protein 1 |
18511
18563 |
| Agammaglobulinemia |
Tyrosine-protein kinase Tec |
18526 |
| Asthma |
Eosinophil cationic protein - trisaccharide heparin mimetic complex |
18596 |
| Ataxia telangiectasia |
Tumor protein P53-binding protein 1 |
18579 |
| Autosomal Dominant Polycystic Kidney Disease |
EF-hand domain of Human Polycystin 2 |
17621 |
| Axenfeld-Rieger syndrome |
Pituitary homeobox protein 2 |
18015 |
| Bloom syndrome |
Rad51D |
16996 |
|
Regulatory HRDC domain from Bloom syndrome protein |
16766 |
| Brain Ischemia |
Postsynaptic density protein 95 |
18516 |
| Cataracts |
P23T mutant of gamma-D crystallin |
16173 |
| Cervicitis |
GPVI mimetic |
18538 |
| Complement component 7 deficiency |
Complement control protein modules of human C7 |
18530 |
| Costello syndrome |
H-Ras-GppNHp bound to Ras-binding domain of cRaf1 |
18461 |
|
H-Ras-GppNHp complex |
18479 |
| DiGeorge syndrome |
DiGeorge Critical Region 8 |
17773 |
| Familial Adenomatous Polyposis |
CH domain of End-binding protein 1 |
18348
18371 |
| Glaucoma |
Optineurin Zinc-finger domain |
18195 |
| Menkes syndrome |
ATPase 7A |
6130
6480
6481
6482
6483
7068
7069
|
|
C30S/C59S-Cox17 mutant |
17821 |
| Mitochondrial disease |
NFU-1 iron sulfur cluster scaffold homolog |
18489 |
| Muckle-Wells syndrome |
Pyrin domain of ASC with NLRP3 protein |
18608 |
| Nodular regenerative hyperplasia |
Zinc finger protein Kaiso |
18630
18631 |
| Nonsyndromic Deafness |
LCCL domain of deafness autosomal dominant type 9 |
5047 |
| Obesity |
Melanocortin receptor 4 agonist |
18536 |
| Oculodentodigital dysplasia |
Connexin 43 |
18552 |
| Polycystic Kidney disease |
Polycystin-2 |
18268 |
| Renal disease |
Bromodomain containing 4 |
18439 |
| Retinal degeneration |
Guanylyl cyclase activating protein 1 |
18026 |
| Short Bowel Syndrome |
Glucagon-like peptide-2 |
17297 |
| Staphyloenterotoxemia |
Epha4 receptor |
18613 |
| Usher's syndrome |
Cadherin 23 |
18441 |
|
Harmonin |
18441 |
| Werner syndrome |
HRDC domain from Werner syndrome protein |
11252 |
|
Werner syndrome protein |
6540 |
