Systematic Identification of Novel Protein Domain Families Associated with Nuclear Functions

Table 2.

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

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

  • ↵Accession number of related protein.

  • ↵Accession number of disease in OMIM database.

This Article

  1. Genome Res. 12: 47-56

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