KEGG   Phyllostomus discolor (pale spear-nosed bat): 114492736
Entry
114492736         CDS       T07739                                 
Symbol
TGFB3
Name
(RefSeq) transforming growth factor beta-3 proprotein
  KO
K13377  transforming growth factor beta-3
Organism
pdic  Phyllostomus discolor (pale spear-nosed bat)
Pathway
pdic04010  MAPK signaling pathway
pdic04060  Cytokine-cytokine receptor interaction
pdic04068  FoxO signaling pathway
pdic04110  Cell cycle
pdic04218  Cellular senescence
pdic04350  TGF-beta signaling pathway
pdic04390  Hippo signaling pathway
pdic04933  AGE-RAGE signaling pathway in diabetic complications
pdic05140  Leishmaniasis
pdic05142  Chagas disease
pdic05144  Malaria
pdic05145  Toxoplasmosis
pdic05146  Amoebiasis
pdic05152  Tuberculosis
pdic05161  Hepatitis B
pdic05166  Human T-cell leukemia virus 1 infection
pdic05200  Pathways in cancer
pdic05210  Colorectal cancer
pdic05211  Renal cell carcinoma
pdic05212  Pancreatic cancer
pdic05220  Chronic myeloid leukemia
pdic05225  Hepatocellular carcinoma
pdic05226  Gastric cancer
pdic05321  Inflammatory bowel disease
pdic05323  Rheumatoid arthritis
pdic05410  Hypertrophic cardiomyopathy
pdic05414  Dilated cardiomyopathy
pdic05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:pdic00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04010 MAPK signaling pathway
    114492736 (TGFB3)
   04350 TGF-beta signaling pathway
    114492736 (TGFB3)
   04390 Hippo signaling pathway
    114492736 (TGFB3)
   04068 FoxO signaling pathway
    114492736 (TGFB3)
  09133 Signaling molecules and interaction
   04060 Cytokine-cytokine receptor interaction
    114492736 (TGFB3)
 09140 Cellular Processes
  09143 Cell growth and death
   04110 Cell cycle
    114492736 (TGFB3)
   04218 Cellular senescence
    114492736 (TGFB3)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    114492736 (TGFB3)
  09162 Cancer: specific types
   05210 Colorectal cancer
    114492736 (TGFB3)
   05212 Pancreatic cancer
    114492736 (TGFB3)
   05225 Hepatocellular carcinoma
    114492736 (TGFB3)
   05226 Gastric cancer
    114492736 (TGFB3)
   05220 Chronic myeloid leukemia
    114492736 (TGFB3)
   05211 Renal cell carcinoma
    114492736 (TGFB3)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    114492736 (TGFB3)
   05161 Hepatitis B
    114492736 (TGFB3)
  09171 Infectious disease: bacterial
   05152 Tuberculosis
    114492736 (TGFB3)
  09174 Infectious disease: parasitic
   05146 Amoebiasis
    114492736 (TGFB3)
   05144 Malaria
    114492736 (TGFB3)
   05145 Toxoplasmosis
    114492736 (TGFB3)
   05140 Leishmaniasis
    114492736 (TGFB3)
   05142 Chagas disease
    114492736 (TGFB3)
  09163 Immune disease
   05323 Rheumatoid arthritis
    114492736 (TGFB3)
   05321 Inflammatory bowel disease
    114492736 (TGFB3)
  09166 Cardiovascular disease
   05410 Hypertrophic cardiomyopathy
    114492736 (TGFB3)
   05414 Dilated cardiomyopathy
    114492736 (TGFB3)
   05415 Diabetic cardiomyopathy
    114492736 (TGFB3)
  09167 Endocrine and metabolic disease
   04933 AGE-RAGE signaling pathway in diabetic complications
    114492736 (TGFB3)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04052 Cytokines and neuropeptides [BR:pdic04052]
    114492736 (TGFB3)
Cytokines and neuropeptides [BR:pdic04052]
 Cytokines
  Transforming growth factors (RSTK binding)
   114492736 (TGFB3)
SSDB
Motif
Pfam: TGFb_propeptide TGF_beta
Other DBs
NCBI-GeneID: 114492736
NCBI-ProteinID: XP_028363036
UniProt: A0A6J2L6G7
LinkDB
Position
1:complement(197675337..197696119)
AA seq 408 aa
MKMHLQRALAVLALLNFATVSVSLSTCTTLDFSHIKKKRVEAIRGQILSKLRLTSPPEPS
VMTHVPYQILALYNSTRELLEEREDGCTQENTEWEYYAKEIHKFDMIQGLAEHNELAVCP
KGITSKVFRFNVSSVEKNGTNLFRAEFRVLRVPNPSSKRNEQRIELFQILRPDEHIAKQR
YIGGKNLPTRGTAEWLSFDVTETVREWLSRRESNLGLEISIHCPCHTFQPNGDILENIHE
VMEIKFKGVDSEDDHGRGDLGRLRKQKDHHNPHLILMMIPPHRLDNGGQGGQRKKRALDT
NYCFSNVEENCCVRPLYIDFRQDLGWKWVHEPKGYYANFCSGPCPYLRSADTTHSKVLGL
YNTLNPEASASPCCVPQDLEPLTILYYVGRTPKVEHLSNMVVKSCKCS
NT seq 1227 nt   +upstreamnt  +downstreamnt
atgaagatgcacttgcaaagggctctggcggtcctggccctgctgaactttgccacggtc
agcgtctctctgtccacttgcaccaccttggacttcagccacatcaagaagaagagggtg
gaagccattaggggacagatcttgagcaaactcaggctcactagtccccctgagccttcg
gtgatgacccatgtcccctaccagatcctggccctttacaacagcacccgggagctgctg
gaggagagggaggacggctgcactcaggagaacaccgagtgggagtactatgccaaagaa
atccataaattcgacatgatccaggggctggcggaacacaacgagctggccgtctgcccc
aaaggaatcacctccaaggtgttccgcttcaacgtgtcctccgtggagaagaatggcacc
aacctcttccgagcagaattccgggtcttgcgggtgcccaaccccagctccaagcgcaat
gagcagaggatcgagctcttccagatactccggccagatgagcacattgccaagcagcgc
tatattggtggcaagaatctgcccacgcggggcaccgccgagtggctgtctttcgatgtc
actgaaaccgtacgtgaatggctctcgagaagagagtccaacttaggtctggaaatcagc
attcattgtccctgccacacctttcagcccaatggagacatcctggaaaacattcatgag
gtgatggaaatcaaattcaaaggtgtggacagcgaggatgatcatggccgtggggatctg
ggacgcctcaggaagcagaaggaccaccacaaccctcatctaatcctcatgatgatcccc
ccacaccggctcgacaacgggggccagggtgggcagaggaagaagcgggccctggacacc
aattactgctttagcaacgtggaagagaactgctgtgtgcgccctctctacatcgacttc
cgccaggatctgggctggaaatgggtccacgaacctaagggctactacgccaacttctgc
tcaggcccctgcccatacctccgcagtgcagacaccacccacagcaaggtgctgggcctg
tacaacaccttgaaccccgaagcgtctgcctccccgtgctgcgtgccccaggacttggag
cccttgaccatcctgtactacgtcgggaggacccccaaggtggaacacctctctaacatg
gtggtgaagtcctgtaagtgtagctga

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