Physeter macrocephalus (sperm whale): 114484267 Help Entry 114484267         CDS       T06011                                  Symbol WNT7A Name (RefSeq) protein Wnt-7a   KO K00572   wingless-type MMTV integration site family, member 7 Organism pcad  Physeter macrocephalus (sperm whale) Pathway pcad04150   mTOR signaling pathway pcad04310   Wnt signaling pathway pcad04390   Hippo signaling pathway pcad04550   Signaling pathways regulating pluripotency of stem cells pcad04916   Melanogenesis pcad04934   Cushing syndrome pcad05010   Alzheimer disease pcad05022   Pathways of neurodegeneration - multiple diseases pcad05165   Human papillomavirus infection pcad05200   Pathways in cancer pcad05205   Proteoglycans in cancer pcad05217   Basal cell carcinoma pcad05224   Breast cancer pcad05225   Hepatocellular carcinoma pcad05226   Gastric cancer Brite KEGG Orthology (KO) [BR:pcad00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     114484267 (WNT7A)    04390 Hippo signaling pathway     114484267 (WNT7A)    04150 mTOR signaling pathway     114484267 (WNT7A)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     114484267 (WNT7A)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     114484267 (WNT7A)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     114484267 (WNT7A)    05205 Proteoglycans in cancer     114484267 (WNT7A)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     114484267 (WNT7A)    05226 Gastric cancer     114484267 (WNT7A)    05217 Basal cell carcinoma     114484267 (WNT7A)    05224 Breast cancer     114484267 (WNT7A)   09172 Infectious disease: viral    05165 Human papillomavirus infection     114484267 (WNT7A)   09164 Neurodegenerative disease    05010 Alzheimer disease     114484267 (WNT7A)    05022 Pathways of neurodegeneration - multiple diseases     114484267 (WNT7A)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     114484267 (WNT7A)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:pcad00536]     114484267 (WNT7A) Glycosaminoglycan binding proteins [BR:pcad00536]  Heparan sulfate / Heparin   Morphogens    114484267 (WNT7A) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  wnt DUF6973 Motif Other DBs NCBI-GeneID:  114484267 NCBI-ProteinID:  XP_028335191 UniProt:  A0A455ATH6 LinkDB All DBs Position 18:complement(7443183..7492893) Genome browser AA seq 266 aa AA seqDB search MDGWRFRWPLTQGICDGSREAAFTYAIIAAGVAHAITAACTQGNLSDCGCDKEKQGQYHR DEGWKWGGCSADIRYGIGFAKVFVDAREIKQNARTLMNLHNNEAGRKILEENMKLECKCH GVSGSCTTKTCWTTLPQFRELGYVLKDKYNEAVHVEPVRASRNKRPTFLKIKKPLSYRKP MDTDLVYIEKSPNYCEEDPVTGSVGTQGRACNKTAPQASGCDLMCCGRGYNTHQYARVWQ CNCKFHWCCYVKCNTCSERTEVYTCK NT seq 801 nt NT seq  +upstreamnt  +downstreamnt atggatggatggaggttcaggtggcctctcacgcaaggaatctgcgatgggagccgggag gccgccttcacctacgccatcatcgcagccggcgtggcccacgccatcacggctgcctgc acccagggcaacctgagcgactgcggctgcgacaaggagaagcaaggccagtaccaccgg gacgagggctggaagtggggtggctgctctgccgacatccgctacggcatcggcttcgcc aaggtctttgtggatgcccgggagatcaagcagaatgcccggactctcatgaacttacac aataacgaggcaggccgaaagatcctggaggagaacatgaagctggagtgcaagtgccac ggcgtgtcgggctcatgcaccaccaagacctgctggaccacgctgccgcagttccgcgag ctgggctacgtgctcaaggacaagtacaacgaggctgtccacgtggagcccgtgcgcgcc agccgcaacaagcggcccaccttcctgaagatcaagaagccactgtcctaccgcaagccc atggacaccgacctggtgtacatcgagaagtcgcccaactactgcgaggaggacccggtg acgggcagcgtgggcacgcagggccgagcctgcaacaagacggccccccaggccagcggc tgcgacctcatgtgctgcggccgcggctacaacacccaccagtacgcccgcgtgtggcag tgcaactgcaagttccactggtgctgctacgtcaagtgcaacacgtgcagcgagcgcacc gaggtctacacgtgcaagtga

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