Vulpes vulpes (red fox): 112930056 Help Entry 112930056         CDS       T05911                                  Symbol BMP2 Name (RefSeq) bone morphogenetic protein 2   KO K21283   bone morphogenetic protein 2 Organism vvp  Vulpes vulpes (red fox) Pathway vvp04060   Cytokine-cytokine receptor interaction vvp04350   TGF-beta signaling pathway vvp04390   Hippo signaling pathway vvp05200   Pathways in cancer vvp05217   Basal cell carcinoma Brite KEGG Orthology (KO) [BR:vvp00001]  09130 Environmental Information Processing   09132 Signal transduction    04350 TGF-beta signaling pathway     112930056 (BMP2)    04390 Hippo signaling pathway     112930056 (BMP2)   09133 Signaling molecules and interaction    04060 Cytokine-cytokine receptor interaction     112930056 (BMP2)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     112930056 (BMP2)   09162 Cancer: specific types    05217 Basal cell carcinoma     112930056 (BMP2)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04052 Cytokines and neuropeptides [BR:vvp04052]     112930056 (BMP2)    00536 Glycosaminoglycan binding proteins [BR:vvp00536]     112930056 (BMP2) Cytokines and neuropeptides [BR:vvp04052]  Cytokines   Transforming growth factors (RSTK binding)    112930056 (BMP2) Glycosaminoglycan binding proteins [BR:vvp00536]  Heparan sulfate / Heparin   Morphogens    112930056 (BMP2) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  TGFb_propeptide TGF_beta Peptidase_M24_C Motif Other DBs NCBI-GeneID:  112930056 NCBI-ProteinID:  XP_025868079 UniProt:  A0A3Q7SW70 LinkDB All DBs Position Unknown AA seq 395 aa AA seqDB search MVAGTRCLLALLLPQVLLGGAAGLITELGRRKFAASPGRSSSQPSDEVLSEFELRLLSMF GLKRRPTPSRDAVVPPYMLDLYRRHSGQPGAPAPDQRLERAASLANTVRSFHHEESLEEL PEMSGKTTRRFFFNLTSIPTDEFITSAELQVFREQMQEPLENNSNFHHRINIYEIIKPAA ANLKFPVTRLLDTRLVNQNTSRWESFDVTPAVMRWTAQGLANHGFVVEVTHLEENQGVSK RHVRISRSLHQDEHSWSQIRPLLVTFGHDGKGHPLHKREKRQAKHKQRKRLKSSCKRHPL YVDFSDVGWNDWIVAPPGYHAFYCHGECPFPLADHLNSTNHAIVQTLVNSVNSKIPKACC VPTELSAISMLYLDENEKVVLKNYQDMVVEGCGCR NT seq 1188 nt NT seq  +upstreamnt  +downstreamnt atggtggccgggacccgctgtcttctagcgttgctgcttccccaggtcctcctgggcggc gcggccggtctcattacggagctgggccggaggaagttcgcggcatctcctggccgctcc tcgtcccagccctcggacgaagtcctgagcgagttcgagttgcggctgctcagcatgttc ggcctgaagcggagacccacccccagcagggacgccgtggtgcccccctacatgctggac ctgtaccgccggcactcgggccagccgggcgcaccggccccggaccagcggctggagagg gcagccagcctcgccaacaccgtgcgcagcttccaccacgaagaatctttggaagaactg ccagaaatgagtgggaaaacaacccggagattcttctttaatttaacttctatccccact gacgagtttatcacctcagcagaacttcaggtttttcgggaacagatgcaggaacctttg gaaaacaatagcaatttccatcaccgaattaatatttatgaaattataaaacctgcagca gccaacttgaagttccccgtgaccagacttttggacaccaggttggtgaatcagaacaca agcaggtgggagagctttgatgtcacccctgctgtgatgaggtggacggcacaggggctt gccaaccacggatttgtggtggaagtgacccacttggaggagaatcaaggtgtctccaag agacacgtcaggattagcaggtctttgcaccaagacgagcacagctggtcacaaatcagg ccactgctagtaacgtttggccacgatgggaaaggacaccccctccacaaaagagaaaag cgtcaagcaaaacacaaacagcgcaaacgccttaagtccagctgtaagagacaccctttg tacgtggacttcagtgacgtggggtggaatgactggatcgtagctcccccggggtaccac gccttttattgccatggggaatgcccctttcccctggcagatcacctgaactccactaac cacgccattgttcagacgttggtcaactcggttaattctaagatccccaaggcgtgctgt gtaccaacagaactcagtgctatctccatgctgtaccttgatgaaaacgaaaaggttgta ttaaagaactatcaggacatggttgtggagggttgtgggtgtcgttag

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