KEGG   Peromyscus leucopus (white-footed mouse): 114699199
Entry
114699199         CDS       T07241                                 
Symbol
Wnt7b
Name
(RefSeq) protein Wnt-7b isoform X1
  KO
K00572  wingless-type MMTV integration site family, member 7
Organism
pleu  Peromyscus leucopus (white-footed mouse)
Pathway
pleu04150  mTOR signaling pathway
pleu04310  Wnt signaling pathway
pleu04390  Hippo signaling pathway
pleu04550  Signaling pathways regulating pluripotency of stem cells
pleu04916  Melanogenesis
pleu04934  Cushing syndrome
pleu05010  Alzheimer disease
pleu05022  Pathways of neurodegeneration - multiple diseases
pleu05165  Human papillomavirus infection
pleu05200  Pathways in cancer
pleu05205  Proteoglycans in cancer
pleu05217  Basal cell carcinoma
pleu05224  Breast cancer
pleu05225  Hepatocellular carcinoma
pleu05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:pleu00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    114699199 (Wnt7b)
   04390 Hippo signaling pathway
    114699199 (Wnt7b)
   04150 mTOR signaling pathway
    114699199 (Wnt7b)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    114699199 (Wnt7b)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    114699199 (Wnt7b)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    114699199 (Wnt7b)
   05205 Proteoglycans in cancer
    114699199 (Wnt7b)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    114699199 (Wnt7b)
   05226 Gastric cancer
    114699199 (Wnt7b)
   05217 Basal cell carcinoma
    114699199 (Wnt7b)
   05224 Breast cancer
    114699199 (Wnt7b)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    114699199 (Wnt7b)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    114699199 (Wnt7b)
   05022 Pathways of neurodegeneration - multiple diseases
    114699199 (Wnt7b)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    114699199 (Wnt7b)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:pleu00536]
    114699199 (Wnt7b)
Glycosaminoglycan binding proteins [BR:pleu00536]
 Heparan sulfate / Heparin
  Morphogens
   114699199 (Wnt7b)
SSDB
Motif
Pfam: wnt DUF6973 DUF7259
Other DBs
NCBI-GeneID: 114699199
NCBI-ProteinID: XP_028733973
LinkDB
Position
20:18909411..18955999
AA seq 353 aa
MLLLSPRSALVSVYCPQIFLLLSSGSYLALSSVVALGANIICNKIPGLAPRQRAICQSRP
DAIIVIGEGAQMGINECQHQFRFGRWNCSALGEKTVFGQELRVGSREAAFTYAITAAGVA
HAVTAACSQGNLSNCGCDREKQGYYNQAEGWKWGGCSADVRYGIDFSRRFVDAREIKKNA
RRLMNLHNNEAGRKVLEDRMKLECKCHGVSGSCTTKTCWTTLPKFREVGHLLKEKYNAAV
QVEVVRASRLRQPTFLRIKQLRSYQKPMETDLVYIEKSPNYCEEDAATGSVGTQGRLCNR
TSPGADGCDTMCCGRGYNTHQYTKVWQCNCKFHWCCFVKCNTCSERTEVFTCK
NT seq 1062 nt   +upstreamnt  +downstreamnt
atgctcctcttgtcgccgcgcagcgcgctggtctccgtctattgcccgcagatctttctc
cttctgtccagcggcagctacctggcattgtcgtccgtggtggccctaggagccaacatc
atctgcaacaagattcctggcctggccccacggcagcgtgccatctgccagagccgaccc
gatgccatcattgtgatcggggagggggcgcagatgggcatcaatgagtgccagcaccag
ttccgatttggccgctggaactgctccgccctgggcgagaagaccgtcttcgggcaagag
ctccgagtagggagtcgcgaggctgccttcacatacgccatcaccgcggcaggcgtggca
cacgccgtcaccgcggcctgcagccagggcaacctgagcaactgcggctgtgaccgcgag
aagcaaggctactacaaccaggcggaaggctggaaatggggaggatgctcggcggatgtg
cgctatggcattgacttctcccgacgcttcgtggatgctcgtgagatcaagaagaatgcc
cggcgtctcatgaacctccacaacaacgaggcaggcagaaaggttctggaggaccgcatg
aagcttgaatgtaagtgtcacggtgtgtcgggctcgtgtaccaccaaaacctgctggacc
acgctgcccaagttccgggaggtgggccacctgctcaaggagaaatacaacgcagccgtg
caggtggaggtggtgcgagccagccgcctgcgccagcccaccttcctgcgcatcaagcag
ctgcgcagctaccagaagcccatggagacggacctggtgtacatcgagaagtcgcccaac
tactgcgaagaggacgcggccacgggcagcgtgggcacgcagggccgcctgtgcaaccgc
acctctcccggcgccgacggctgcgacaccatgtgctgcggccgcggctacaacacgcac
cagtacaccaaggtgtggcagtgcaactgcaaattccactggtgttgcttcgtcaagtgc
aacacgtgcagcgagcgcacggaggtcttcacctgcaagtga

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