FGFR1OP2 (NP_056448, 62 a.a. ~ 169 a.a) partial recombinant protein with GST tag. The sequence is RSTLVMGIQQENRQIRELQQENKELRTSLEEHQSALELIMSKYREQMFRLLMASKKDDPG IIMKLKEQHSKIDMVHRNKSEGFFLDASRHILEAPQHGLERRHLEANQ
FGFR1OP2 (FGFR1 oncogene partner 2) is a protein-coding gene. Diseases associated with FGFR1OP2 include cerebral cavernous malformations 3, and cavernous malformation, and among its related super-pathways are Signaling by FGFR1 mutants and Signaling by FGFR. GO annotations related to this gene include protein homodimerization activity. An important paralog of this gene is SIKE1.
Pathway
Disease; Signaling by FGFR mutants; Signaling by FGFR1 mutants;
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