2cr3
From Proteopedia
Solution structure of the first Ig-like domain of human fibroblast growth factor receptor 1
Disease
Known disease associated with this structure: Antley-Bixler syndrome OMIM:[136350], Hypogonadotropic hypogonadism OMIM:[136350], Jackson-Weiss syndrome OMIM:[136350], Kallmann syndrome 2 OMIM:[136350], Osteoglophonic dysplasia OMIM:[136350], Pfeiffer syndrome OMIM:[136350], Trigonocephaly OMIM:[136350]
About this Structure
2CR3 is a 1 chain structure of sequence from Homo sapiens. Full experimental information is available from OCA.
Page seeded by OCA on Tue Feb 17 21:53:01 2009
Categories: Homo sapiens | Transferase | Hatta, R. | Hayashi, F. | RSGI, RIKEN Structural Genomics/Proteomics Initiative. | Yokoyama, S. | Yoshida, M. | Bfgf-r | Fgfr1 | Ig fold | National project on protein structural and functional analyse | Nppsfa | Riken structural genomics/proteomics initiative | Rsgi | Structural genomic
