| S.NO | Uniprot ID | Protein Name | Sequence Length | PAS Repeats region | Disease |
| 1 | P56645 | Period circadian protein homolog 3 | 1201 | "DISEASE: Advanced sleep phase syndrome, familial, 3 (FASPS3) [MIM:616882]: A disorder characterized by very early sleep onset and offset. Individuals are 'morning larks' with a 4 hours advance of the sleep, temperature and melatonin rhythms. Note=The disease is caused by mutations affecting the gene represented in this entry". | |
| 2 | Q99814 | Endothelial PAS domain-containing protein 1 | 870 | "DISEASE: Erythrocytosis, familial, 4 (ECYT4) [MIM:611783]: An autosomal dominant disorder characterized by increased serum red blood cell mass, elevated serum hemoglobin and hematocrit, and normal platelet and leukocyte counts. Note=The disease is caused by mutations affecting the gene represented in this entry". | |
| 3 | O15055 | Period circadian protein homolog 2 | 1255 | "DISEASE: Advanced sleep phase syndrome, familial, 1 (FASPS1) [MIM:604348]: A disorder characterized by very early sleep onset and offset. Individuals are 'morning larks' with a 4 hours advance of the sleep, temperature and melatonin rhythms. Note=The disease is caused by mutations affecting the gene represented in this entry". | |
| 4 | Q8IXF0 | Neuronal PAS domain-containing protein 3 | 933 | DISEASE: Note=A chromosomal aberration involving NPAS3 is found in a family with schizophrenia. Translocation t(9;14)(q34;q13). | |
| 5 | Q9HBZ2 | Aryl hydrocarbon receptor nuclear translocator 2 | 717 | "DISEASE: Webb-Dattani syndrome (WEDAS) [MIM:615926]: A disorder characterized by postnatal microcephaly with fronto-temporal lobe hypoplasia, multiple pituitary hormone deficiency, global developmental delay, seizures, severe visual impairment and abnormalities of the kidneys and urinary tract. Note=The disease is caused by mutations affecting the gene represented in this entry". | |