Piliocolobus tephrosceles (Ugandan red Colobus): 111546455
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Entry
111546455 CDS
T07491
Symbol
BMP2
Name
(RefSeq) bone morphogenetic protein 2 isoform X1
KO
K21283
bone morphogenetic protein 2
Organism
pteh
Piliocolobus tephrosceles (Ugandan red Colobus)
Pathway
pteh04060
Cytokine-cytokine receptor interaction
pteh04350
TGF-beta signaling pathway
pteh04390
Hippo signaling pathway
pteh05200
Pathways in cancer
pteh05217
Basal cell carcinoma
Brite
KEGG Orthology (KO) [BR:
pteh00001
]
09130 Environmental Information Processing
09132 Signal transduction
04350 TGF-beta signaling pathway
111546455 (BMP2)
04390 Hippo signaling pathway
111546455 (BMP2)
09133 Signaling molecules and interaction
04060 Cytokine-cytokine receptor interaction
111546455 (BMP2)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
111546455 (BMP2)
09162 Cancer: specific types
05217 Basal cell carcinoma
111546455 (BMP2)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04052 Cytokines and neuropeptides [BR:
pteh04052
]
111546455 (BMP2)
00536 Glycosaminoglycan binding proteins [BR:
pteh00536
]
111546455 (BMP2)
Cytokines and neuropeptides [BR:
pteh04052
]
Cytokines
Transforming growth factors (RSTK binding)
111546455 (BMP2)
Glycosaminoglycan binding proteins [BR:
pteh00536
]
Heparan sulfate / Heparin
Morphogens
111546455 (BMP2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
TGFb_propeptide
TGF_beta
CBM96
Peptidase_M24_C
Motif
Other DBs
NCBI-GeneID:
111546455
NCBI-ProteinID:
XP_023073639
Ensembl:
ENSPTEG00000003872
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All DBs
Position
20:complement(55398712..55411092)
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AA seq
396 aa
AA seq
DB search
MVAGTRCLLALLLPQVLLGGAAGLVPELGRRKFAASSSGRPSSQPSDEVLSEFELRLLSM
FGLKQRPTPSRDAVVPPYMLDLYRRQSGQPGSPAPDHRLERAASRANTVRSFHHEESLEE
LPEMSGKTTRRFFFNLSSIPTEEFITSAELQVFREQMQDALGDNSSFHHRINIYEIIKPA
TANSKFPVTRLLDTRLVNQNASRWESFDVTPAVMRWTAQGHANHGFVVEVTHLEEKQGVS
KRHVRISRSLHQDEHSWSQIRPLLVTFGHDGKGHPLHKREKRQAKHKQRKRLKSSCKRHP
LYVDFSDVGWNDWIVAPPGYHAFYCHGECPFPLADHLNSTNHAIVQTLVNSVNSKIPKAC
CVPTELSAISMLYLDENEKVVLKNYQDMVVEGCGCR
NT seq
1191 nt
NT seq
+upstream
nt +downstream
nt
atggtggccgggacccgctgtcttctagcgttgctgcttccccaggtcctcctgggcggc
gcggctggcctcgttccggagctgggccgcaggaagttcgcggcgtcgtcgtcgggccgc
ccctcatcccagccctctgacgaggtcctgagcgagttcgagttgcggctgctcagcatg
ttcggcctgaaacagagacccacccccagcagggacgccgtggtgcccccctacatgcta
gacctgtatcgcaggcaatcgggtcagccgggctcacccgccccagaccaccggttggag
agggcagccagccgagccaacactgtgcgcagcttccaccatgaagaatctttggaagaa
ctaccagaaatgagtgggaaaacaactcggagattcttctttaatttaagttctatcccc
acggaggagtttatcacctcagcagagcttcaggtttttcgagagcagatgcaagatgct
ttaggagacaatagcagtttccatcaccgaattaatatttatgaaatcataaaacctgca
acagccaactcgaaattccccgtgaccagacttttggacaccagattggtgaatcagaat
gcaagcaggtgggaaagttttgacgtcacccccgcagtgatgcggtggactgcacaggga
catgccaaccatggattcgtggtggaagtgacccacttggaggagaagcaaggtgtctcc
aagagacatgttaggataagcaggtctttgcaccaagatgaacacagctggtcacagata
aggccgctgctagtaacttttggccatgatgggaaagggcatcctctccacaaaagagaa
aaacgtcaagcaaaacacaaacagcggaaacgccttaagtccagctgtaagagacaccct
ttgtacgtggacttcagtgacgtggggtggaatgactggattgtggctcccccggggtat
cacgccttttactgccacggagaatgcccttttcctctggctgatcatctgaactccact
aatcatgccattgttcagacgttggtcaactctgttaactctaagattcctaaggcgtgc
tgtgtcccaacggaactcagtgctatctcgatgctgtaccttgacgaaaatgaaaaggtt
gtattaaagaactatcaggacatggttgtggagggttgtgggtgtcgctag
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