KEGG   Cricetulus griseus (Chinese hamster): 100755799
Entry
100755799         CDS       T02813                                 
Symbol
Wnt7b
Name
(RefSeq) protein Wnt-7b isoform X1
  KO
K00572  wingless-type MMTV integration site family, member 7
Organism
cge  Cricetulus griseus (Chinese hamster)
Pathway
cge04150  mTOR signaling pathway
cge04310  Wnt signaling pathway
cge04390  Hippo signaling pathway
cge04519  Cadherin signaling
cge04550  Signaling pathways regulating pluripotency of stem cells
cge04916  Melanogenesis
cge04934  Cushing syndrome
cge05010  Alzheimer disease
cge05022  Pathways of neurodegeneration - multiple diseases
cge05165  Human papillomavirus infection
cge05200  Pathways in cancer
cge05205  Proteoglycans in cancer
cge05217  Basal cell carcinoma
cge05224  Breast cancer
cge05225  Hepatocellular carcinoma
cge05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:cge00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    100755799 (Wnt7b)
   04390 Hippo signaling pathway
    100755799 (Wnt7b)
   04150 mTOR signaling pathway
    100755799 (Wnt7b)
  09133 Signaling molecules and interaction
   04519 Cadherin signaling
    100755799 (Wnt7b)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    100755799 (Wnt7b)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    100755799 (Wnt7b)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    100755799 (Wnt7b)
   05205 Proteoglycans in cancer
    100755799 (Wnt7b)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    100755799 (Wnt7b)
   05226 Gastric cancer
    100755799 (Wnt7b)
   05217 Basal cell carcinoma
    100755799 (Wnt7b)
   05224 Breast cancer
    100755799 (Wnt7b)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    100755799 (Wnt7b)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100755799 (Wnt7b)
   05022 Pathways of neurodegeneration - multiple diseases
    100755799 (Wnt7b)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    100755799 (Wnt7b)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:cge00536]
    100755799 (Wnt7b)
Glycosaminoglycan binding proteins [BR:cge00536]
 Heparan sulfate / Heparin
  Morphogens
   100755799 (Wnt7b)
SSDB
Motif
Pfam: wnt DUF7259 DUF6973
Other DBs
NCBI-GeneID: 100755799
NCBI-ProteinID: XP_027251981
UniProt: G3ICH8
LinkDB
Position
2:complement(382359773..382404844)
AA seq 353 aa
MLLLSPRSALVSVYCPQIFLLLSSGSYLALSSVVALGANIICNKIPGLAPRQRAICQSRP
DAIIVIGEGAQMGINECQHQFRFGRWNCSALGEKTVFGQELRVGSREAAFTYAITAAGVA
HAVTAACSQGNLSNCGCDREKQGYYNQAEGWKWGGCSADVRYGIDFSRRFVDAREIKKNA
RRLMNLHNNEAGRKVLEDRMKLECKCHGVSGSCTTKTCWTTLPKFREVGHLLKEKYNAAV
QVEVVRASRLRQPTFLRIKQLRSYQKPMETDLVYIEKSPNYCEEDAATGSVGTQGRLCNR
TSPGADGCDTMCCGRGYNTHQYTKVWQCNCKFHWCCFVKCNTCSERTEVFTCK
NT seq 1062 nt   +upstreamnt  +downstreamnt
atgctcctcctgtcgccgcgcagcgcgctggtctccgtctattgcccgcagatctttctc
cttctgtccagcggcagctacctagcactgtcgtccgtggtggccctaggagccaacatc
atctgcaacaagattcctggcctggcccctcggcagcgcgccatctgccagagccgcccc
gatgccatcattgtgatcggggagggggctcagatgggcatcaatgagtgccaacaccag
ttccgattcggccgctggaactgctccgccctgggcgagaagaccgtcttcgggcaagag
ctccgagtagggagtcgtgaggctgccttcacatacgccatcaccgcggcaggcgtggca
catgctgtcactgctgcctgcagccagggtaacctgagcaactgtggctgtgaccgtgag
aagcaaggctactacaaccaggctgaaggctggaagtggggaggctgctcggctgatgtg
cgctatggcattgacttttcccgacgatttgtggatgctcgtgagatcaaaaagaacgcc
aggcgcctcatgaacctccacaacaatgaggcaggcagaaaggttctggaggaccgcatg
aagcttgaatgtaagtgtcacggtgtgtcgggctcgtgtaccaccaagacctgctggacc
acgctgcccaagttccgtgaggtgggccacctgctcaaggagaaatacaacgcagccgtg
caggtggaggtggtacgcgccagccgtctgcgccagcccaccttcctgcgcatcaagcag
ctgcgcagctaccagaagcccatggagacggacctggtgtacattgagaagtcgcccaac
tactgcgaggaggacgcagccacgggcagcgtgggcacgcagggccgcctgtgcaaccgc
acctctccaggcgccgacggctgcgacaccatgtgctgcggccgcggctacaacacgcac
cagtacaccaaggtgtggcagtgcaactgcaaattccactggtgttgcttcgtcaagtgc
aacacatgcagcgagcgcaccgaggtcttcacctgcaagtga

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