KEGG   Cercocebus atys (sooty mangabey): 105586922
Entry
105586922         CDS       T07242                                 
Symbol
WNT7B
Name
(RefSeq) protein Wnt-7b isoform X1
  KO
K00572  wingless-type MMTV integration site family, member 7
Organism
caty  Cercocebus atys (sooty mangabey)
Pathway
caty04150  mTOR signaling pathway
caty04310  Wnt signaling pathway
caty04390  Hippo signaling pathway
caty04550  Signaling pathways regulating pluripotency of stem cells
caty04916  Melanogenesis
caty04934  Cushing syndrome
caty05010  Alzheimer disease
caty05022  Pathways of neurodegeneration - multiple diseases
caty05165  Human papillomavirus infection
caty05200  Pathways in cancer
caty05205  Proteoglycans in cancer
caty05217  Basal cell carcinoma
caty05224  Breast cancer
caty05225  Hepatocellular carcinoma
caty05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:caty00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    105586922 (WNT7B)
   04390 Hippo signaling pathway
    105586922 (WNT7B)
   04150 mTOR signaling pathway
    105586922 (WNT7B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    105586922 (WNT7B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    105586922 (WNT7B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    105586922 (WNT7B)
   05205 Proteoglycans in cancer
    105586922 (WNT7B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    105586922 (WNT7B)
   05226 Gastric cancer
    105586922 (WNT7B)
   05217 Basal cell carcinoma
    105586922 (WNT7B)
   05224 Breast cancer
    105586922 (WNT7B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    105586922 (WNT7B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    105586922 (WNT7B)
   05022 Pathways of neurodegeneration - multiple diseases
    105586922 (WNT7B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    105586922 (WNT7B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:caty00536]
    105586922 (WNT7B)
Glycosaminoglycan binding proteins [BR:caty00536]
 Heparan sulfate / Heparin
  Morphogens
   105586922 (WNT7B)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 105586922
NCBI-ProteinID: XP_011917929
Ensembl: ENSCATG00000045374
UniProt: A0A2K5P8L3
LinkDB
Position
Unknown
AA seq 353 aa
MLLLSPRSALVSVYCPQIFLLLSSGSYLALSSVVALGANIICNKIPGLAPRQRAICQSRP
DAIIVIGEGAQMGINECQYQFRFGRWNCSALGEKTVFGQELRVGSREAAFTYAITAAGVA
HAVTAACSQGNLSNCGCDREKQGYYNQAEGWKWGGCSADVRYGIDFSRRFVDAREIKKNA
RRLMNLHNNEAGRKVLEDRMQLECKCHGVSGSCTTKTCWTTLPKFREVGHLLKEKYNAAV
QVEVVRASRLRQPTFLRIKQLRSYQKPMETDLVYIEKSPNYCEEDAATGSVGTQGRLCNR
TSPGADGCDTMCCGRGYNTHQYTKVWQCNCKFHWCCFVKCNTCSERTEVFTCK
NT seq 1062 nt   +upstreamnt  +downstreamnt
atgctcctactgtcgccgcgcagcgcgctcgtctccgtctattgcccgcagatctttctc
ctcctgtccagcggcagctacctagcactgtcatcagtggtggccctgggagccaacatc
atctgcaacaagattcctggcctagccccgcggcagcgtgccatctgccagagccggccc
gatgccatcattgtgatcggggagggggcgcagatgggcatcaacgagtgccagtaccag
ttccgctttggacgctggaactgctctgccctcggcgagaagactgtctttgggcaagag
ctccgagtagggagccgtgaggctgccttcacgtatgccatcaccgcggctggcgtagca
cacgccgtcactgctgcctgcagccaaggcaacctgagcaactgcggctgtgaccgcgag
aagcagggctactacaaccaggctgagggctggaagtggggtggctgctcggccgacgtg
cgttacggcatcgacttctcccggcgcttcgtggacgctcgggagatcaagaagaacgcg
cggcgcctcatgaacctgcacaacaatgaggccggcaggaaggttctggaggaccgaatg
cagctggagtgcaagtgtcacggcgtgtctggctcctgcaccaccaagacctgctggacc
acgctacccaagttccgagaggtgggccacctgctgaaggagaagtacaacgcggccgtg
caggtggaggtggtgcgggccagccgcctgcggcagcccaccttcctgcgcatcaaacag
ctgcgcagctatcagaagcccatggagacggacctggtgtacatcgagaagtcacccaac
tactgcgaggaggacgcggccacgggcagcgtgggcacgcagggccgcctctgcaaccgc
acgtcgcccggtgcggacggctgtgacaccatgtgctgcggccgaggctacaacacccac
cagtacaccaaggtgtggcagtgcaactgcaaattccactggtgctgcttcgtcaagtgc
aacacctgcagcgagcgcaccgaggtcttcacctgcaagtga

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