KEGG   Arvicola amphibius (Eurasian water vole): 119823832
Entry
119823832         CDS       T08327                                 
Symbol
Wnt7b
Name
(RefSeq) protein Wnt-7b isoform X1
  KO
K00572  wingless-type MMTV integration site family, member 7
Organism
aamp  Arvicola amphibius (Eurasian water vole)
Pathway
aamp04150  mTOR signaling pathway
aamp04310  Wnt signaling pathway
aamp04390  Hippo signaling pathway
aamp04550  Signaling pathways regulating pluripotency of stem cells
aamp04916  Melanogenesis
aamp04934  Cushing syndrome
aamp05010  Alzheimer disease
aamp05022  Pathways of neurodegeneration - multiple diseases
aamp05165  Human papillomavirus infection
aamp05200  Pathways in cancer
aamp05205  Proteoglycans in cancer
aamp05217  Basal cell carcinoma
aamp05224  Breast cancer
aamp05225  Hepatocellular carcinoma
aamp05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:aamp00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    119823832 (Wnt7b)
   04390 Hippo signaling pathway
    119823832 (Wnt7b)
   04150 mTOR signaling pathway
    119823832 (Wnt7b)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    119823832 (Wnt7b)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    119823832 (Wnt7b)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    119823832 (Wnt7b)
   05205 Proteoglycans in cancer
    119823832 (Wnt7b)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    119823832 (Wnt7b)
   05226 Gastric cancer
    119823832 (Wnt7b)
   05217 Basal cell carcinoma
    119823832 (Wnt7b)
   05224 Breast cancer
    119823832 (Wnt7b)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    119823832 (Wnt7b)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    119823832 (Wnt7b)
   05022 Pathways of neurodegeneration - multiple diseases
    119823832 (Wnt7b)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    119823832 (Wnt7b)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:aamp00536]
    119823832 (Wnt7b)
Glycosaminoglycan binding proteins [BR:aamp00536]
 Heparan sulfate / Heparin
  Morphogens
   119823832 (Wnt7b)
SSDB
Motif
Pfam: wnt DUF6973 DUF7259
Other DBs
NCBI-GeneID: 119823832
NCBI-ProteinID: XP_038199822
LinkDB
Position
9:complement(43913646..43955570)
AA seq 353 aa
MLLLSPRSALVSVYCPQIFLLLSSGSYLALSSVVALGANIICNKIPGLAPRQRAICQSRP
DAIIVIGEGAQMGINECQHQFRFGRWNCSALGEKTVFGQELRVGSREAAFTYAITAAGVA
HAVTAACSQGNLSNCGCDREKQGYYNQAEGWKWGGCSADVRYGIDFSRRFVDAREIKKNA
RRLMNLHNNEAGRKVLEDRMKLECKCHGVSGSCTTKTCWTTLPKFREVGHLLKEKYNAAV
QVEVVRASRLRQPTFLRIKQLRSYQKPMETDLVYIEKSPNYCEEDAATGSVGTQGRLCNR
TSPGADGCDTMCCGRGYNTHQYTKVWQCNCKFHWCCFVKCNTCSERTEVFTCK
NT seq 1062 nt   +upstreamnt  +downstreamnt
atgctcctcctgtcgccgcgcagcgcgctggtctccgtctattgcccgcagatctttctc
cttctgtccagcggcagctacctagcactgtcatccgtggtggccctgggagccaatatc
atctgcaacaagattcctggcctggccccacggcagcgtgccatctgccagagccgaccc
gatgccatcattgtgatcggggagggggcgcagatgggcatcaatgaatgccagcaccag
ttccgattcggccgctggaactgctccgctctgggcgagaagaccgtcttcgggcaagag
ctccgagtagggagtcgtgaggccgccttcacatatgccatcaccgcagcaggcgtggcc
catgccgtcactgctgcctgcagccagggcaacctgagcaactgtggctgtgaccgggag
aagcaaggctactacaaccaggcagaaggctggaagtggggaggctgctcagccgatgtg
cgctacggcatcgacttttcccgacgcttcgtagatgctcgcgagattaaaaagaatgcc
aggcgcctcatgaacctccacaacaatgaggcaggcagaaaggttctggaggaccgcatg
aagcttgaatgtaagtgtcacggtgtgtcgggctcgtgcaccaccaaaacctgctggacc
actctgcccaagttccgtgaggtgggccacctgctcaaggagaaatacaacgcagccgtg
caggtggaggtggtgcgcgccagccgcctgcgccagcccaccttcctgcgcataaagcaa
ctgcgcagctaccagaagcctatggagacggacctggtgtacatcgagaagtcgcccaac
tactgtgaggaggacgcggccacgggcagcgtgggcacgcaggggcgactgtgcaaccgc
acctctcccggcgccgacggctgtgacaccatgtgctgtggccgcggctacaacacgcac
cagtataccaaggtgtggcagtgcaactgcaaattccactggtgttgctttgtcaagtgc
aacacgtgcagcgagcgcaccgaggtcttcacctgcaagtga

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