KEGG   Neogale vison (American mink): 122891888
Entry
122891888         CDS       T08764                                 
Symbol
WNT7B
Name
(RefSeq) protein Wnt-7b isoform X1
  KO
K00572  wingless-type MMTV integration site family, member 7
Organism
nvs  Neogale vison (American mink)
Pathway
nvs04150  mTOR signaling pathway
nvs04310  Wnt signaling pathway
nvs04390  Hippo signaling pathway
nvs04550  Signaling pathways regulating pluripotency of stem cells
nvs04916  Melanogenesis
nvs04934  Cushing syndrome
nvs05010  Alzheimer disease
nvs05022  Pathways of neurodegeneration - multiple diseases
nvs05165  Human papillomavirus infection
nvs05200  Pathways in cancer
nvs05205  Proteoglycans in cancer
nvs05217  Basal cell carcinoma
nvs05224  Breast cancer
nvs05225  Hepatocellular carcinoma
nvs05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:nvs00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    122891888 (WNT7B)
   04390 Hippo signaling pathway
    122891888 (WNT7B)
   04150 mTOR signaling pathway
    122891888 (WNT7B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    122891888 (WNT7B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    122891888 (WNT7B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    122891888 (WNT7B)
   05205 Proteoglycans in cancer
    122891888 (WNT7B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    122891888 (WNT7B)
   05226 Gastric cancer
    122891888 (WNT7B)
   05217 Basal cell carcinoma
    122891888 (WNT7B)
   05224 Breast cancer
    122891888 (WNT7B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    122891888 (WNT7B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    122891888 (WNT7B)
   05022 Pathways of neurodegeneration - multiple diseases
    122891888 (WNT7B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    122891888 (WNT7B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:nvs00536]
    122891888 (WNT7B)
Glycosaminoglycan binding proteins [BR:nvs00536]
 Heparan sulfate / Heparin
  Morphogens
   122891888 (WNT7B)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 122891888
NCBI-ProteinID: XP_044083841
LinkDB
Position
12:3615660..3663521
AA seq 356 aa
MAQPPSLDHAQKLSQVDFLRVSLLWRPLREARSAVVRRGPGSQHHLQQDPWLGPAAARHL
PEPARCHHRDWGGGADGHQRVPVPVPLRTLELLRPRRENRLRARAPRSREAAFTYAITAA
GVAHAVTAACSQGNLSNCGCDREKQGYYNQAEGWKWGGCSADVRYGIDFSRRFVDAREIK
KNARRLMNLHNNEAGRKVLEERMKLECKCHGVSGSCTTKTCWTTLPKFREVGHMLKEKYN
AAVQVEVVRASRLRQPTFLRIKQLRSYQKPMETDLVYIEKSPNYCEEDAATGSVGTQGRL
CNRTSPGADGCDTMCCGRGYNTHQYTKVWQCNCKFHWCCFVKCNTCSERTEVFTCK
NT seq 1071 nt   +upstreamnt  +downstreamnt
atggcgcagcccccctccctggatcatgcacagaaactttcgcaagtggattttctacgt
gtttctctgctttggcgtcctctacgtgaagctcggagcgctgtcgtccgtcgtggccct
gggagccaacatcatctgcaacaagatccctggcttggccccgcggcagcgcgccatctg
ccagagccggcccgatgccatcatcgtgattggggagggggcgcagatgggcatcaacga
gtgccagtaccagttccgcttcggacgctggaactgctccgccctcggcgagaaaaccgt
cttcgggcaagagctccgaggagccgcgaggccgccttcacctatgccatcaccgcggct
ggcgtggcgcacgccgtcacggccgcctgcagccaggggaacctgagcaactgcgggtgt
gaccgcgagaagcagggctactacaaccaggccgagggctggaagtggggcgggtgctcc
gccgacgtgcgctacggcatcgacttctcccggcgcttcgtggatgcccgcgagatcaag
aagaacgcgcggcgcctcatgaacctgcacaacaacgaggcgggcaggaaggtcctggag
gagcgcatgaagctggagtgcaaatgccacggcgtgtcgggctcgtgcaccaccaagacg
tgctggaccacgctgcccaagttccgcgaggtgggccacatgctcaaggagaagtacaac
gcggcggtgcaggtggaggtggtgcgggccagccgcctgcggcagcccaccttcctgcgc
atcaagcagctgcgcagctaccagaagcccatggagacggacctggtgtacatcgagaag
tcgcccaactactgcgaggaggacgcggccacgggcagcgtgggcacgcagggccgcctg
tgcaaccgcacgtcgccgggcgcggacggctgcgacaccatgtgctgcggccgcggctac
aacacgcaccagtacaccaaggtgtggcagtgcaactgcaagttccactggtgctgcttc
gtcaagtgcaacacgtgcagcgagcgcaccgaggtcttcacctgcaagtga

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