Gene table: search width pubmed_id = 14517542


Grey lines background indicate newly added items
Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Congenital cataracts, facial dysmorphism and neuropathy - (AR)
14.134
14517542
CTDP1 (18q23)
CTD phosphatase subunit 1
* congenital cataracts, facial dysmorphism, and neuropathy - CCFDN