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. 2002 Jan;12(1):47–56. doi: 10.1101/gr.203201

Table 2.

Table of Novel Domains or Family-Specific Extensions Which are Putatively Correlated with Phenotypic Dysfunctions

Domain name Protein acc. No.a Disease OMIM Acc.Nov.b
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
a

Accession number of related protein. 

b

Accession number of disease in OMIM database.