Table of Novel Domains or Family-Specific Extensions Which are Putatively Correlated with Phenotypic Dysfunctions
| Domain name | Protein acc. No.[i] | Disease | OMIM Acc.Nov.[ii] |
| AWS | O96028 | Wolf-Hirschhorn syndrome (Stec et al. 1998) | 602952 |
| RWD | CAB88085 | Monosomy 21 (Orti et al. 2000) | --- |
| DNP | O70656 | Malignent astrocytoma (Nakamura et al. 1998) | --- |
| FYRN/FYRC | Q03164 | Acute leukemia (Djabali et al. 1992) | 159555 |
[i] Accession number of related protein.
[ii] Accession number of disease in OMIM database.