KEGG   Colobus angolensis palliatus (Angola colobus): 105506562
Entry
105506562         CDS       T08744                                 
Symbol
WNT7B
Name
(RefSeq) protein Wnt-7b
  KO
K00572  wingless-type MMTV integration site family, member 7
Organism
cang  Colobus angolensis palliatus (Angola colobus)
Pathway
cang04150  mTOR signaling pathway
cang04310  Wnt signaling pathway
cang04390  Hippo signaling pathway
cang04550  Signaling pathways regulating pluripotency of stem cells
cang04916  Melanogenesis
cang04934  Cushing syndrome
cang05010  Alzheimer disease
cang05022  Pathways of neurodegeneration - multiple diseases
cang05165  Human papillomavirus infection
cang05200  Pathways in cancer
cang05205  Proteoglycans in cancer
cang05217  Basal cell carcinoma
cang05224  Breast cancer
cang05225  Hepatocellular carcinoma
cang05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:cang00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    105506562 (WNT7B)
   04390 Hippo signaling pathway
    105506562 (WNT7B)
   04150 mTOR signaling pathway
    105506562 (WNT7B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    105506562 (WNT7B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    105506562 (WNT7B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    105506562 (WNT7B)
   05205 Proteoglycans in cancer
    105506562 (WNT7B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    105506562 (WNT7B)
   05226 Gastric cancer
    105506562 (WNT7B)
   05217 Basal cell carcinoma
    105506562 (WNT7B)
   05224 Breast cancer
    105506562 (WNT7B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    105506562 (WNT7B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    105506562 (WNT7B)
   05022 Pathways of neurodegeneration - multiple diseases
    105506562 (WNT7B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    105506562 (WNT7B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:cang00536]
    105506562 (WNT7B)
Glycosaminoglycan binding proteins [BR:cang00536]
 Heparan sulfate / Heparin
  Morphogens
   105506562 (WNT7B)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 105506562
NCBI-ProteinID: XP_011790149
Ensembl: ENSCANG00000015161
UniProt: A0A2K5HJ68
LinkDB
Position
Unknown
AA seq 353 aa
MLLLSPRSALVSVYCPQIFLLLSSGSYLALSSVVALGANIICNKIPGLAPRQRAICQSRP
DAIIVIGEGAQMGINECQYQFRFGRWNCSALGEKTVFGQELRVGSREAAFTYAITAAGVA
HAVTAACSQGNLSNCGCDREKQGYYNQAEGWKWGGCSADVRYGIDFSRRFVDAREIKKNA
RRLMNLHNNEAGRKVLEDRMQLECKCHGVSGSCTTKTCWTTLPKFREVGHLLKEKYNAAV
QVEVVRASRLRQPTFLRIKQLRSYQKPMETDLVYIEKSPNYCEEDAATGSVGTQGRLCNR
TSPGADGCDTMCCGRGYNTHQYTKVWQCNCKFHWCCFVKCNTCSERTEVFTCK
NT seq 1062 nt   +upstreamnt  +downstreamnt
atgctcctactgtcgccgcgcagcgcgctcgtctccgtctattgcccgcagatctttctc
ctcctgtccagcggcagctacctagcactgtcatcagtggtggccctgggagccaacatc
atctgcaacaagattcctggcctagccccgcggcagcgtgccatctgccagagccggcct
gatgccatcattgtgatcggggagggggcgcagatgggcatcaacgagtgccagtaccag
ttccgctttggacgctggaactgctctgccctcggcgagaagactgtctttgggcaagag
ctccgagtagggagccgtgaggctgccttcacgtatgccatcaccgcggctggcgtagcg
cacgccgtcactgctgcctgcagccaaggcaacctgagcaactgcggctgtgaccgcgag
aagcagggctactacaaccaggccgagggctggaagtggggtggctgctcggctgacgtg
cgttacggcatcgacttctcccggcgcttcgtggacgctcgggagatcaagaagaacgcg
cggcgcctcatgaacctgcacaacaatgaggccggcaggaaggttctggaggaccggatg
cagctggagtgcaagtgtcacggcgtgtctggctcctgcaccaccaagacctgctggacc
acgctgcccaagttccgagaggtgggccacctgctgaaggagaagtacaacgcggccgtg
caggtggaggtggtgcgggccagccgcctgcggcagcccaccttcctgcgcatcaaacag
ctgcgcagctatcagaagcccatggagacggacctggtgtacatcgagaagtcgcccaac
tactgcgaggaggacgcggccacgggcagcgtgggcacgcagggccgcctctgcaaccgc
acgtcgcccggtgcggacggctgtgacaccatgtgctgcggccgaggctacaacacccac
cagtacaccaaggtgtggcagtgcaactgcaaattccactggtgctgcttcgtcaagtgc
aacacctgcagtgaacgcaccgaggtcttcacctgcaagtga

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