KEGG   Heterocephalus glaber (naked mole-rat): 101701972
Entry
101701972         CDS       T02812                                 
Symbol
Wnt4
Name
(RefSeq) Wnt family member 4
  KO
K00408  wingless-type MMTV integration site family, member 4
Organism
hgl  Heterocephalus glaber (naked mole-rat)
Pathway
hgl04150  mTOR signaling pathway
hgl04310  Wnt signaling pathway
hgl04360  Axon guidance
hgl04390  Hippo signaling pathway
hgl04550  Signaling pathways regulating pluripotency of stem cells
hgl04916  Melanogenesis
hgl04919  Thyroid hormone signaling pathway
hgl04934  Cushing syndrome
hgl05010  Alzheimer disease
hgl05022  Pathways of neurodegeneration - multiple diseases
hgl05165  Human papillomavirus infection
hgl05200  Pathways in cancer
hgl05205  Proteoglycans in cancer
hgl05217  Basal cell carcinoma
hgl05224  Breast cancer
hgl05225  Hepatocellular carcinoma
hgl05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:hgl00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    101701972 (Wnt4)
   04390 Hippo signaling pathway
    101701972 (Wnt4)
   04150 mTOR signaling pathway
    101701972 (Wnt4)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    101701972 (Wnt4)
 09150 Organismal Systems
  09152 Endocrine system
   04919 Thyroid hormone signaling pathway
    101701972 (Wnt4)
   04916 Melanogenesis
    101701972 (Wnt4)
  09158 Development and regeneration
   04360 Axon guidance
    101701972 (Wnt4)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    101701972 (Wnt4)
   05205 Proteoglycans in cancer
    101701972 (Wnt4)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    101701972 (Wnt4)
   05226 Gastric cancer
    101701972 (Wnt4)
   05217 Basal cell carcinoma
    101701972 (Wnt4)
   05224 Breast cancer
    101701972 (Wnt4)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    101701972 (Wnt4)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    101701972 (Wnt4)
   05022 Pathways of neurodegeneration - multiple diseases
    101701972 (Wnt4)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    101701972 (Wnt4)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:hgl00536]
    101701972 (Wnt4)
Glycosaminoglycan binding proteins [BR:hgl00536]
 Heparan sulfate / Heparin
  Morphogens
   101701972 (Wnt4)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 101701972
NCBI-ProteinID: XP_012929868
LinkDB
Position
Un
AA seq 296 aa
MCKRNLEVMDSVRRGAQLAIEECQYQFRNRRWNCSTLDSLPVFGKVVTQGTREAAFVYAI
SSAGVAFAVTRACSSGELEKCGCDRTVHGVSPQGFQWSGCSDNIAYGVAFSQSFVDVRER
SKGSSSSRALMNLHNNEAGRKAILSHMRVECKCHGVSGSCEVKTCWRAVPPFRQVGHALK
EKFDGATEVEPRRVGSSRALVPRNAQFKPHTDEDLVYLEPSPDFCEQDIRSGVLGTRGRT
CNKTSKAIDGCELLCCGRGFHTAQVELAERCSCKFHWCCFVKCRQCQRLVELHTCR
NT seq 891 nt   +upstreamnt  +downstreamnt
atgtgcaagaggaacctggaggtgatggactcagtgcgtcgcggagcccagctggccatc
gaggagtgccagtaccagtttcggaaccggcgctggaactgctccacactcgattccctg
cctgtctttggcaaggtggtgacgcaagggactcgggaggcggcctttgtgtatgccatc
tcttcagcaggtgtggcctttgcagtaactcgggcatgtagcagtggggagctggaaaag
tgtggatgtgatcggacggtacatggtgtcagccctcagggcttccagtggtcaggatgc
tcggacaacatcgcctatggcgtagccttctcacagtcatttgtggatgtgcgggagaga
agcaaggggtcctcatccagccgggccctcatgaacctccacaacaacgaggccggaagg
aaggctatcctatcacacatgcgggtggagtgcaagtgccacggggtatcaggctcctgc
gaagtaaagacatgctggcgagctgtgccacccttccgccaggtgggccacgcacttaag
gagaagttcgacggcgccaccgaggtggagccacgccgtgtgggctcctctagggcactg
gtgccacgcaatgcacagttcaagccacacacagacgaggacttggtgtacttggagccc
agcccagatttttgtgagcaggacatacgcagcggcgtgctgggcacgagaggccgcaca
tgcaataagacatccaaggccatcgatggctgtgagctgctgtgctgtggtcgcggcttc
cacacggctcaggtagagctggctgaacgctgcagctgcaaattccactggtgctgcttc
gtcaaatgccggcaatgccagcggctcgtagaattgcacacgtgccggtga

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