Puma concolor (puma): 112869247 Help Entry 112869247         CDS       T08890                                  Symbol BMP2 Name (RefSeq) bone morphogenetic protein 2   KO K21283   bone morphogenetic protein 2 Organism pcoo  Puma concolor (puma) Pathway pcoo04060   Cytokine-cytokine receptor interaction pcoo04350   TGF-beta signaling pathway pcoo04390   Hippo signaling pathway pcoo05200   Pathways in cancer pcoo05217   Basal cell carcinoma Brite KEGG Orthology (KO) [BR:pcoo00001]  09130 Environmental Information Processing   09132 Signal transduction    04350 TGF-beta signaling pathway     112869247 (BMP2)    04390 Hippo signaling pathway     112869247 (BMP2)   09133 Signaling molecules and interaction    04060 Cytokine-cytokine receptor interaction     112869247 (BMP2)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     112869247 (BMP2)   09162 Cancer: specific types    05217 Basal cell carcinoma     112869247 (BMP2)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04052 Cytokines and neuropeptides [BR:pcoo04052]     112869247 (BMP2)    00536 Glycosaminoglycan binding proteins [BR:pcoo00536]     112869247 (BMP2) Cytokines and neuropeptides [BR:pcoo04052]  Cytokines   Transforming growth factors (RSTK binding)    112869247 (BMP2) Glycosaminoglycan binding proteins [BR:pcoo00536]  Heparan sulfate / Heparin   Morphogens    112869247 (BMP2) SSDB OrthologParalogGFIT Motif Pfam:  TGFb_propeptide TGF_beta CBM96 Motif Other DBs NCBI-GeneID:  112869247 NCBI-ProteinID:  XP_025788130 UniProt:  A0A6P6IIT6 LinkDB All DBs Position Unknown AA seq 395 aa AA seqDB search MVAGTRCLLALLLPQVLLGGAAGLIPELGRRKFAASTGRSSSQPSDEVLSEFELRLLSMF GLKRRPTPSRDAVVPPYMLDLYRRHSGQPGAPAPDHRLERAASLANTVRSFHHEESVEEL PEMSGKTTRRFFFNLTSIPTDEFITSAELQVFREQMQETLENNSSFHHRINIYEIIKPAT ANLKFPMTRLLDTRLVNQNTSRWESFDVTPAVMRWTTQGLTNHGFVVEVTHLEENQGVSK RHVRISRSLHQDEHSWSQIRPLLVTFGHDGKGHPLHKREKRQAKHKQRKRLKSSCKRHPL YVDFSDVGWNDWIVAPPGYHAFYCHGECPFPLADHLNSTNHAIVQTLVNSVNSKIPKACC VPTELSAISMLYLDENEKVVLKNYQDMVVEGCGCR NT seq 1188 nt NT seq  +upstreamnt  +downstreamnt atggtggccgggacccgctgtcttctagcgttgctgcttccccaggtcctcctgggcggc gcggccggcctcattcccgagctgggccggaggaagttcgcggcatcaactggccgctcc tcgtcccagccctcggacgaagtcctgagcgagtttgagttgcggctgctcagcatgttc ggcctgaagcggagacccacccccagcagggacgccgtggtgcccccctacatgctggac ctgtatcgccggcactcgggccagccgggcgcccccgcccccgaccaccggctggagagg gcagccagcctcgccaacaccgtgcgcagtttccaccacgaagaatctgtggaagaactg cctgaaatgagtggaaaaacaacccggagattcttctttaatttaacttctatccccacc gatgagtttatcacctcagcagaacttcaggtttttcgggaacagatgcaggaaactttg gaaaacaatagcagtttccatcaccgaattaatatttatgaaattataaaacctgcaaca gccaacttgaagttccctatgaccagacttttggacaccaggttggtgaatcagaacaca agcaggtgggagagttttgacgtcacccctgctgtgatgaggtggaccacacagggactc accaaccacggatttgtggtggaagtgacccacttggaggagaaccaaggtgtctccaag agacacgtcaggattagcaggtctttgcaccaagatgagcacagctggtcacagatcagg ccactgctagtaacttttggccacgacgggaaagggcaccctctccacaaaagagaaaag cgtcaagcaaaacacaaacagcgcaaacgccttaagtccagctgtaagagacaccctttg tatgtggacttcagtgacgtggggtggaatgactggatcgtagctcccccagggtaccat gccttttattgccacggggaatgcccttttcccctggcagatcacctgaactccactaat cacgccattgttcagacgttggtcaactctgttaattctaaaattcctaaggcatgctgt gtaccaacggaactcagtgctatctccatgctgtaccttgatgaaaatgaaaaggtcgta ttaaagaactatcaggacatggttgtggagggttgtgggtgtcgttag

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