Table 3 |
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WDR genes associated with human disease and their Arabidopsis homologs. |
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|
Human disease |
Human gene and function |
Arabidopsis gene(s), expect (E) value, and function if known |
|
|
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|
Chediak-Higashi syndrome (CHS) [85] |
LYST (ENSG00000143669) involved in protein trafficking [86] |
At4g02660 (3E-98) At1g03060 (3E-85) |
|
sensorineural deafness [87] |
TBL1 (ENSG00000092377) component of SMRT and NCOR corepressor complexes [88] |
At5g67320 (1E-104) |
|
Cockayne's syndrome [89] |
CSA (ENSG00000049167) transcription-coupled DNA repair [89] |
At1g27840 (6E-55) At1g19750 (2E-33) |
|
Triple-A syndrome (AAAS) [90] |
ALADIN (ENS00000094914) nucleoporin [9] |
At3g56900 (1E-29) |
|
Refsum disease, rhizomelic chondrodysplasia punctata (RCDP) [91] |
PEX7 (ENSG00000112357) peroxisomal receptor for type-2 peroxisomal targeting signals [92] |
PEX7/At1g29260 (2E-74) Peroxisomal receptor for type-2 peroxisomal targeting signals [73] |
|
|
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van Nocker and Ludwig BMC Genomics 2003 4:50 doi:10.1186/1471-2164-4-50 |
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