KEGG   Microtus fortis (reed vole): 126509605
Entry
126509605         CDS       T08493                                 
Name
(RefSeq) protein Wnt-4
  KO
K00408  wingless-type MMTV integration site family, member 4
Organism
mfot  Microtus fortis (reed vole)
Pathway
mfot04150  mTOR signaling pathway
mfot04310  Wnt signaling pathway
mfot04360  Axon guidance
mfot04390  Hippo signaling pathway
mfot04550  Signaling pathways regulating pluripotency of stem cells
mfot04916  Melanogenesis
mfot04919  Thyroid hormone signaling pathway
mfot04934  Cushing syndrome
mfot05010  Alzheimer disease
mfot05022  Pathways of neurodegeneration - multiple diseases
mfot05165  Human papillomavirus infection
mfot05200  Pathways in cancer
mfot05205  Proteoglycans in cancer
mfot05217  Basal cell carcinoma
mfot05224  Breast cancer
mfot05225  Hepatocellular carcinoma
mfot05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:mfot00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    126509605
   04390 Hippo signaling pathway
    126509605
   04150 mTOR signaling pathway
    126509605
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    126509605
 09150 Organismal Systems
  09152 Endocrine system
   04919 Thyroid hormone signaling pathway
    126509605
   04916 Melanogenesis
    126509605
  09158 Development and regeneration
   04360 Axon guidance
    126509605
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    126509605
   05205 Proteoglycans in cancer
    126509605
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    126509605
   05226 Gastric cancer
    126509605
   05217 Basal cell carcinoma
    126509605
   05224 Breast cancer
    126509605
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    126509605
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    126509605
   05022 Pathways of neurodegeneration - multiple diseases
    126509605
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    126509605
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:mfot00536]
    126509605
Glycosaminoglycan binding proteins [BR:mfot00536]
 Heparan sulfate / Heparin
  Morphogens
   126509605
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 126509605
NCBI-ProteinID: XP_050011543
LinkDB
Position
Unknown
AA seq 351 aa
MSPRSCLRSLRLLVFAVFSAAASNWLYLAKLSSVGSISEEETCEKLKGLIQRQVQMCKRN
LEVMDSVRRGAQLAIEECQYQFRNRRWNCSTLDSLPVFGKVVTQGTREAAFVYAISSAGV
AFAVTRACSSGELEKCGCDRTVHGVSPQGFQWSGCSDNIAYGVAFSQSFVDVRERSKGAS
SSRALMNLHNNEAGRKAILTHMRVECKCHGVSGSCEVKTCWRAVPPFRQVGHALKEKFDG
ATEVEPRRVGSSRALVPRNAQFKPHTDEDLVYLEPSPDFCEQDIRSGVLGTRGRTCNKTS
KAIDGCELLCCGRGFHTAQVELAERCGCRFHWCCFVKCRQCQRLVEMHTCR
NT seq 1056 nt   +upstreamnt  +downstreamnt
atgagcccccgctcgtgcctgcggtcgctgcgactcctcgtcttcgccgttttctctgcc
gctgcgagcaactggctgtacctggccaagctgtcatcagtgggcagcatctccgaagag
gagacgtgcgagaagctcaaaggtctgatccagaggcaggtgcagatgtgcaagcggaac
ctagaggtgatggactcagtgcgccgtggcgcccagctggccattgaggagtgccaatac
caattccggaatcggcgctggaactgctccacgctggactccctgcctgtcttcgggaag
gtggtgacgcaagggactcgggaggcggcctttgtgtacgccatctcttcagcaggtgtg
gcctttgcggtaacaagggcgtgcagcagtggagagctggaaaagtgcggctgcgaccgg
acagtgcatggggtcagtccacagggcttccagtggtcaggatgctcggacaacatcgcc
tatggcgtagccttctcacagtcctttgtggatgtacgggagagaagcaagggggcctct
tccagcagggcgctcatgaaccttcacaacaacgaggccggcaggaaggccatcttgaca
cacatgcgggtggagtgcaagtgccacggggtgtcgggctcctgtgaggtaaagacgtgc
tggcgagctgtgccgcccttccgccaggtgggccacgctctaaaggagaagtttgatggt
gccacagaggtggagccacgtcgtgtgggctcctcccgggcactggtgccacgaaatgca
cagttcaagccacatacggatgaggacctggtgtacctggagcccagtccagacttctgt
gagcaggacatacgcagtggtgtgctgggcacgagaggccgcacgtgcaacaagacatcc
aaggccattgatggctgtgagctgctgtgttgcggccgtggcttccatacagcacaggtg
gagttggccgagcgctgcggctgcaggttccactggtgctgcttcgtcaagtgccgacag
tgccagcggctcgtggagatgcacacatgccggtga

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