Heterocephalus glaber (naked mole-rat): 101698823 Help Entry 101698823         CDS       T02812                                  Symbol Wnt6 Name (RefSeq) Wnt family member 6   KO K00445   wingless-type MMTV integration site family, member 6 Organism hgl  Heterocephalus glaber (naked mole-rat) Pathway hgl04150   mTOR signaling pathway hgl04310   Wnt signaling pathway hgl04390   Hippo signaling pathway hgl04550   Signaling pathways regulating pluripotency of stem cells hgl04916   Melanogenesis 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     101698823 (Wnt6)    04390 Hippo signaling pathway     101698823 (Wnt6)    04150 mTOR signaling pathway     101698823 (Wnt6)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     101698823 (Wnt6)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     101698823 (Wnt6)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     101698823 (Wnt6)    05205 Proteoglycans in cancer     101698823 (Wnt6)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     101698823 (Wnt6)    05226 Gastric cancer     101698823 (Wnt6)    05217 Basal cell carcinoma     101698823 (Wnt6)    05224 Breast cancer     101698823 (Wnt6)   09172 Infectious disease: viral    05165 Human papillomavirus infection     101698823 (Wnt6)   09164 Neurodegenerative disease    05010 Alzheimer disease     101698823 (Wnt6)    05022 Pathways of neurodegeneration - multiple diseases     101698823 (Wnt6)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     101698823 (Wnt6)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:hgl00536]     101698823 (Wnt6) Glycosaminoglycan binding proteins [BR:hgl00536]  Heparan sulfate / Heparin   Morphogens    101698823 (Wnt6) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Collagen Motif Other DBs NCBI-GeneID:  101698823 NCBI-ProteinID:  XP_012920918 UniProt:  A0A0P6JDQ5 G5AKL4 LinkDB All DBs Position Un AA seq 331 aa AA seqDB search MDPTSICRKARRLAGRQAELCQAEPEVVAELARGARLGVRECQFQFRFRRWNCSSHSKAF GRILQQDIRETAFVFAITAAGASHAVTQACSMGELLQCGCQAPHGRAQSRPPGLPGTPGP PGPVGSSDTSAAWEWGGCGDDVDFGDEKSRLFMDAQHKRGRGDIRALVQLHNNEAGRLAV RSHTRTECKCHGLSGSCALRTCWQKLPPFREVGTRLLERFHGASRVMGTNDGKALLPAVR TLKPPGRADLLYAADSPDFCAPNRRTGSPGTRGRACNSSAPDLSGCDLLCCGRGHRQESV QLEENCLCRFHWCCVVQCHRCRVRKELSLCL NT seq 996 nt NT seq  +upstreamnt  +downstreamnt atggaccctaccagcatctgcaggaaggcacggcggctggcaggacggcaggccgagttg tgccaagcagagccagaagtggtggcagagctagcccggggcgcccggcttggggttcga gagtgtcagttccagttccgcttccgccgctggaactgctccagccacagcaaggctttt gggcgcatcctgcagcaggatattcgggagaccgccttcgtgtttgcaatcactgcagcg ggtgccagccacgcagtgacacaggcctgttccatgggtgagctgttgcagtgcggctgt caggcaccgcacggacgggcccagtcccggccccctggcctgccaggcaccccaggacct ccagggcccgtgggctcctcagacaccagtgccgcctgggagtggggaggctgtggcgac gacgtggactttggggacgagaagtcaaggctgtttatggatgcgcaacacaagcgtgga cgtggagacatccgagctctggtgcaactgcacaacaacgaggctggccggctggccgtt cggagccacacgcgcaccgagtgcaagtgccacggtctgtccggctcatgcgcgctgcgc acctgctggcagaagctgcccccgttccgcgaggtaggcacgcggctgctggagcgcttc cacggtgcctcacgagtcatgggcaccaacgacggcaaagccctgctgccagcggtccgc acgctcaagccaccggggcgcgccgacctcctgtacgcagccgactcgccggacttctgc gcccccaaccggcgcaccggctcgccaggcactcgcggccgcgcctgcaatagcagcgcc ccggacctcagcggttgtgacctgttgtgctgcggccgtgggcaccgccaggagagcgtg cagctcgaggagaactgcctgtgccgcttccactggtgctgcgtagtgcaatgccaccgg tgccgcgtgcgcaaggagctcagcctctgcctctaa

DBGET integrated database retrieval system