KEGG   Mirounga leonina (Southern elephant seal): 117998566
Entry
117998566         CDS       T07472                                 
Symbol
WNT7B
Name
(RefSeq) protein Wnt-7b isoform X1
  KO
K00572  wingless-type MMTV integration site family, member 7
Organism
mlx  Mirounga leonina (Southern elephant seal)
Pathway
mlx04150  mTOR signaling pathway
mlx04310  Wnt signaling pathway
mlx04390  Hippo signaling pathway
mlx04550  Signaling pathways regulating pluripotency of stem cells
mlx04916  Melanogenesis
mlx04934  Cushing syndrome
mlx05010  Alzheimer disease
mlx05022  Pathways of neurodegeneration - multiple diseases
mlx05165  Human papillomavirus infection
mlx05200  Pathways in cancer
mlx05205  Proteoglycans in cancer
mlx05217  Basal cell carcinoma
mlx05224  Breast cancer
mlx05225  Hepatocellular carcinoma
mlx05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:mlx00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    117998566 (WNT7B)
   04390 Hippo signaling pathway
    117998566 (WNT7B)
   04150 mTOR signaling pathway
    117998566 (WNT7B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    117998566 (WNT7B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    117998566 (WNT7B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    117998566 (WNT7B)
   05205 Proteoglycans in cancer
    117998566 (WNT7B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    117998566 (WNT7B)
   05226 Gastric cancer
    117998566 (WNT7B)
   05217 Basal cell carcinoma
    117998566 (WNT7B)
   05224 Breast cancer
    117998566 (WNT7B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    117998566 (WNT7B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    117998566 (WNT7B)
   05022 Pathways of neurodegeneration - multiple diseases
    117998566 (WNT7B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    117998566 (WNT7B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:mlx00536]
    117998566 (WNT7B)
Glycosaminoglycan binding proteins [BR:mlx00536]
 Heparan sulfate / Heparin
  Morphogens
   117998566 (WNT7B)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 117998566
NCBI-ProteinID: XP_034843198
LinkDB
Position
Unknown
AA seq 353 aa
MLLLSPRGALLSVYCPQIFLILSSGSYLALSSVVALGANIICNKIPGLAPRQRAICQSRP
DAIIVIGEGAQMGINECQYQFRFGRWNCSALGEKTVFGQELRVGSREAAFTYAITAAGVA
HAVTAACSQGNLSNCGCDREKQGYYNQAEGWKWGGCSADVRYGIDFSRRFVDAREIKKNA
RRLMNLHNNEAGRKVLEERMKLECKCHGVSGSCTTKTCWTTLPKFREVGHMLKEKYNAAV
QVEVVRASRLRQPTFLRIKQLRSYQKPMETDLVYIEKSPNYCEEDAATGSVGTQGRLCNR
TSPGADGCDTMCCGRGYNTHQYTKVWQCNCKFHWCCFVKCNTCSERTEVFTCK
NT seq 1062 nt   +upstreamnt  +downstreamnt
atgctcctgctgtcgccgcgcggcgcgctcctctccgtgtactgcccgcagatctttctc
atcctgtccagcggcagctacctagcactgtcgtccgtcgtggccctgggagccaacatc
atctgcaacaagattcctggcttggccccacggcagcgcgccatctgccagagccggccc
gatgccatcatcgtgatcggggagggggcgcagatgggcatcaatgagtgccagtaccag
ttccgcttcggacgctggaactgttccgccctcggcgagaagaccgtcttcgggcaagag
ctccgagtagggagccgcgaggccgcgttcacatatgccatcaccgcggccggcgtggcc
cacgccgtcacggccgcctgcagccaggggaacctgagcaactgcgggtgtgaccgcgag
aagcagggctactacaaccaggccgagggctggaagtggggcggctgctcggccgacgtg
cgctacggcatcgacttctcccggcgcttcgtggacgcccgtgagatcaagaagaacgcg
cggcgcctcatgaacctgcacaacaacgaggccggcagaaaggtcctggaggagcgcatg
aagctggagtgcaagtgccacggcgtgtcgggctcgtgcaccaccaagacgtgctggacc
acgctgcccaagttccgcgaggtgggccacatgctcaaggagaagtacaacgcagccgtg
caggtggaggtggtgcgggccagccgcctgcggcagcccaccttcctgcgcatcaagcag
ctgcgcagctaccagaagcccatggagacggacctggtgtacatcgagaagtcgcccaac
tactgcgaggaggacgcggccacgggcagcgtgggcacgcagggccgcctgtgcaaccgc
acgtcgccgggcgcggacggctgcgacaccatgtgctgcggccgtggctacaacacgcac
cagtacaccaaggtgtggcagtgcaactgcaagttccactggtgctgcttcgtcaagtgc
aacacctgcagcgagcgcaccgaggtcttcacctgcaagtga

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