Heterocephalus glaber (naked mole-rat): 101705646 Help Entry 101705646         CDS       T02812                                  Symbol Wnt9b Name (RefSeq) Wnt family member 9B   KO K01064   wingless-type MMTV integration site family, member 9 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     101705646 (Wnt9b)    04390 Hippo signaling pathway     101705646 (Wnt9b)    04150 mTOR signaling pathway     101705646 (Wnt9b)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     101705646 (Wnt9b)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     101705646 (Wnt9b)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     101705646 (Wnt9b)    05205 Proteoglycans in cancer     101705646 (Wnt9b)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     101705646 (Wnt9b)    05226 Gastric cancer     101705646 (Wnt9b)    05217 Basal cell carcinoma     101705646 (Wnt9b)    05224 Breast cancer     101705646 (Wnt9b)   09172 Infectious disease: viral    05165 Human papillomavirus infection     101705646 (Wnt9b)   09164 Neurodegenerative disease    05010 Alzheimer disease     101705646 (Wnt9b)    05022 Pathways of neurodegeneration - multiple diseases     101705646 (Wnt9b)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     101705646 (Wnt9b)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:hgl00536]     101705646 (Wnt9b) Glycosaminoglycan binding proteins [BR:hgl00536]  Heparan sulfate / Heparin   Morphogens    101705646 (Wnt9b) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  101705646 NCBI-ProteinID:  XP_004868854 LinkDB All DBs Position Un AA seq 391 aa AA seqDB search MRPAPALALALAALCLLALPAAAAAAAYFGLQPKFLALSAANALSLRIPRSDARSGSSLG LTGREILTSFPGLDTEAAPTQGSAHLKQCDLLKLSRRQKQLCRREPGLAETLRDAAHLGL LECQFQFQQERWNCSLEGRTGLLKRGFKETAFLYAVSAAALTHALARACSAGRMERCTCD DSPGLESRQAWQWGVCGDNLRYSTKFLTNFLGPKRGSKDLRARADAHNTYVGIKAVKSGL RTTCKCHGVSGSCAVRTCWKQLSPFRETGQVLKLRYDSAVKVSSATNEALGHLELWAPAK PGGPAKGLAPRPVDLVYMEDSPSFCRPSKYSPGTAGRVCSRETSCSSLCCGRGYDTQSRL VAFSCHCQVQWCCYVECQQCMQQELVYTCKR NT seq 1176 nt NT seq  +upstreamnt  +downstreamnt atgcgccccgcgcccgcgctggccctggccctggccgcgctctgcctgctggcgctgccc gccgccgccgccgccgccgcctacttcggactccagcccaagttcctggccctctctgct gcgaatgccctgtccctgcggatcccgcgctccgatgcccgctcgggatcctcactcggc ttgacggggcgggagatcctaacgtccttcccagggctggacaccgaggcagccccaaca cagggcagtgcccacctgaagcagtgtgacctgctgaagctgtcccgccggcagaagcag ctgtgcaggcgggaacctggcctggctgagaccctgagggatgcagcacaccttggcctg ctcgagtgccagttccagttccagcaggagcgctggaactgcagcctggagggaaggact ggcctgctcaagagaggtttcaaggagacagccttcctgtatgcagtgtccgcggccgcc ctcacccatgcactggcccgggcctgcagtgctgggcgaatggagcgctgcacctgcgat gactccccaggcctggaaagccggcaagcctggcagtggggtgtgtgtggtgacaacctc aggtacagcaccaagtttctgaccaacttcctgggccccaagagaggaagcaaggacctg cgggctcgggctgatgcccacaacacctatgtgggcatcaaggcggtgaagagtggcctc cggaccacctgcaagtgccacggagtgtcaggatcctgtgctgtgcgcacctgctggaag cagctctccccattccgtgagacaggccaggtgctgaagctgcgctatgactcagctgtc aaggtgtctagtgccaccaacgaggctttgggccacctggagctgtgggcacctgccaag ccaggtggccctgccaaaggcctggcaccccggccggttgacctggtctacatggaggac tcccccagcttctgccggcccagcaagtattctccaggcacagctggcagggtgtgttcc cgggagaccagctgcagcagcttgtgctgtgggcgtggctatgacacccagagccgcctg gtggccttctcctgccactgccaggttcagtggtgctgctatgtggaatgccagcagtgc atgcagcaggagcttgtgtacacctgtaagcgctag

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