KEGG   Rhinopithecus bieti (black snub-nosed monkey): 108514489
Entry
108514489         CDS       T04641                                 
Symbol
WNT7B
Name
(RefSeq) protein Wnt-7b
  KO
K00572  wingless-type MMTV integration site family, member 7
Organism
rbb  Rhinopithecus bieti (black snub-nosed monkey)
Pathway
rbb04150  mTOR signaling pathway
rbb04310  Wnt signaling pathway
rbb04390  Hippo signaling pathway
rbb04550  Signaling pathways regulating pluripotency of stem cells
rbb04916  Melanogenesis
rbb04934  Cushing syndrome
rbb05010  Alzheimer disease
rbb05022  Pathways of neurodegeneration - multiple diseases
rbb05165  Human papillomavirus infection
rbb05200  Pathways in cancer
rbb05205  Proteoglycans in cancer
rbb05217  Basal cell carcinoma
rbb05224  Breast cancer
rbb05225  Hepatocellular carcinoma
rbb05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:rbb00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    108514489 (WNT7B)
   04390 Hippo signaling pathway
    108514489 (WNT7B)
   04150 mTOR signaling pathway
    108514489 (WNT7B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    108514489 (WNT7B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    108514489 (WNT7B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    108514489 (WNT7B)
   05205 Proteoglycans in cancer
    108514489 (WNT7B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    108514489 (WNT7B)
   05226 Gastric cancer
    108514489 (WNT7B)
   05217 Basal cell carcinoma
    108514489 (WNT7B)
   05224 Breast cancer
    108514489 (WNT7B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    108514489 (WNT7B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    108514489 (WNT7B)
   05022 Pathways of neurodegeneration - multiple diseases
    108514489 (WNT7B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    108514489 (WNT7B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:rbb00536]
    108514489 (WNT7B)
Glycosaminoglycan binding proteins [BR:rbb00536]
 Heparan sulfate / Heparin
  Morphogens
   108514489 (WNT7B)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 108514489
NCBI-ProteinID: XP_017706234
UniProt: A0A2K6MD94
LinkDB
Position
Unknown
AA seq 353 aa
MLLLSPRSALVSVYCPQIFLLLSSGSYLALSSVVALGANIICNKIPGLAPRQRAICQSRP
DAIIVIGEGAQMGINECQYQFRFGRWNCSALGEKTVFGQELRVGSREAAFTYAITAAGVA
HAVTAACSQGNLSNCGCDREKQGYYNQAEGWKWGGCSADVRYGIDFSRRFVDAREIKKNA
RRLMNLHNNEAGRKVLEDRMQLECKCHGVSGSCTTKTCWTTLPKFREVGHLLKEKYNAAV
QVEVVRASRLRQPTFLRIKQLRSYQKPMETDLVYIEKSPNYCEEDAATGSVGTQGRLCNR
TSPGADGCDTMCCGRGYNTHQYTKVWQCNCKFHWCCFVKCNTCSERTEVFTCK
NT seq 1062 nt   +upstreamnt  +downstreamnt
atgctcctactgtcgccgcgcagcgcgctcgtctccgtctattgcccgcagatctttctc
ctcctgtccagcggcagctacctagcactgtcatcagtggtggccctgggagccaacatc
atctgcaacaagattcctggcctagccccgcggcagcgtgccatctgccagagccggccc
gatgccatcattgtgatcggggagggggcgcagatgggcatcaacgagtgccagtaccag
ttccgctttggacgctggaactgctctgccctcggcgagaagactgtctttgggcaagag
ctccgagtagggagccgtgaggctgccttcacgtatgccatcaccgcggctggcgtagcg
cacgccgtcactgccgcctgcagccaaggcaacctgagcaactgcggctgtgaccgcgag
aagcagggctactacaaccaggccgagggctggaagtggggtggctgctcagccgacgtg
cgttacggcatcgacttctcccggcgcttcgtggacgctcgggagatcaagaagaacgcg
cggcgcctcatgaacctgcacaacaatgaggccggcaggaaggttctggaggaccggatg
cagctggagtgcaagtgtcacggtgtgtctggctcctgcaccaccaagacctgctggacc
acgctgcccaagttccgagaggtgggccacctgctgaaggagaagtacaacgcggccgtg
caggtggaggtggtgcgggccagccgcctgcggcagcccaccttcctgcgcatcaaacag
ctgcgcagctatcagaagcccatggagacggacctggtgtacatcgagaagtcgcccaac
tactgcgaggaggacgcggccacgggaagcgtgggcactcagggccgcctctgcaaccgc
acgtcgcccggtgcggacggctgtgacaccatgtgctgcggccgaggctacaacacccac
cagtacaccaaggtgtggcagtgcaactgcaaattccactggtgctgcttcgtcaagtgc
aacacctgcagcgagcgcaccgaggtcttcacctgcaagtga

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