A cDNA sequencing project was initiated with the aim of isolating and
mapping new genes expressed during early human development. A human em
bryo cDNA library was constructed, and a prescreening procedure was us
ed to select cDNAs corresponding to poorly transcribed genes. Partial
sequences were generated from one or both ends of 231 cDNA clones, and
sequence comparison with genetic databases revealed that 28% were alr
eady annotated genes, 42% matched with partial sequences expressed seq
uence tags that had already been detected, 3% contained no insert, 5%
were highly similar to sequences hom other species, and 23% of the cDN
As appeared to be unknown in genetic databases. All new sequences were
deposited in public genetic databases, and most of the corresponding
cDNAs were regionally mapped on human chromosome bands using both fluo
rescence and radioactive in situ hybridization. Several cDNAs colocali
zed with critical regions of the genome regarding mapped disorders, th
us providing candidate genes for human genetic diseases. (C) 1997 Acad
emic Press