Equus asinus (ass): 106827683 Help Entry 106827683         CDS       T04645                                  Symbol PSEN1 Name (RefSeq) presenilin-1 isoform X1   KO K04505   presenilin 1 [EC:3.4.23.-] Organism eai  Equus asinus (ass) Pathway eai04310   Wnt signaling pathway eai04330   Notch signaling pathway eai04722   Neurotrophin signaling pathway eai05010   Alzheimer disease eai05022   Pathways of neurodegeneration - multiple diseases eai05165   Human papillomavirus infection Brite KEGG Orthology (KO) [BR:eai00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     106827683 (PSEN1)    04330 Notch signaling pathway     106827683 (PSEN1)  09150 Organismal Systems   09156 Nervous system    04722 Neurotrophin signaling pathway     106827683 (PSEN1)  09160 Human Diseases   09172 Infectious disease: viral    05165 Human papillomavirus infection     106827683 (PSEN1)   09164 Neurodegenerative disease    05010 Alzheimer disease     106827683 (PSEN1)    05022 Pathways of neurodegeneration - multiple diseases     106827683 (PSEN1)  09180 Brite Hierarchies   09181 Protein families: metabolism    01002 Peptidases and inhibitors [BR:eai01002]     106827683 (PSEN1) Peptidases and inhibitors [BR:eai01002]  Aspartic peptidases   Family A22: presenilin family    106827683 (PSEN1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Presenilin Motif Other DBs NCBI-GeneID:  106827683 NCBI-ProteinID:  XP_014691159 UniProt:  A0A8C4LDK6 LinkDB All DBs Position 7:46471537..46545137 Genome browser AA seq 470 aa AA seqDB search MTELPAPLSYFQNAQMSEDNHLSNSVRSQNENRDRHEHSSERRRRGNPEPLSNGRPQSNS NSQQVVEQDEEEDEELTLKYGAKHVIMLFVPVTLCMVVVVATIKSVSFYTRKDGQLIYTP FTEDTDTVGQRALHSILNAAIMISVIVVMTILLVVLYKYRCYKVIHAWLIISSLLLLFFF SIIYLGEVFKTYNVAMDYITVALLIWNFGVVGMIAIHWKGPLRLQQAYLIMISALMALVF IKYLPEWTAWLILAVISIYDLVAVLCPKGPLRLLVETAQERNETLFPALIYSSTMVWLVN MAEGDPEAQRKVSKNSNYNAQSTESESQDPVTESDDGGFSEEWEAQRDSRLGPHRSTTES RAAAQELSSSILASEDPEERGVKLGLGDFIFYSVLVGKASATASGDWNTTIACFVAILIG LCLTLLLLAIFKKALPALPISITFGLVFYFATDYLVQPFMDQLAFHQFYV NT seq 1413 nt NT seq  +upstreamnt  +downstreamnt atgacagagttacctgcacccttgtcctacttccagaatgcacagatgtctgaggacaac cacctgagcaatagcgtacgtagtcagaatgagaacagagaccggcatgagcacagtagc gaaaggcggaggcgtggcaaccctgagccattatctaatggacgaccccagagtaactct aactcacagcaggtggtggagcaagatgaagaagaagatgaggagctgacgctgaaatat ggcgccaaacatgtgatcatgctctttgtcccagtgactctctgtatggtggtggttgtg gctaccatcaaatcagtcagcttttatacgcggaaggatgggcagctaatctatacccca ttcacagaagacaccgatactgtggggcagagagccctgcactcaattctgaatgctgct atcatgatcagcgtcatagttgtcatgactattctcctggtggttctgtacaaatacagg tgctataaggtcatccatgcctggcttattatttcatctctgttgttgctgttctttttc tcaatcatttacttgggggaagtgtttaaaacctacaacgttgccatggactacattact gttgcacttctgatctggaattttggcgtggtgggaatgattgccattcactggaaaggt ccgctgcgactccagcaggcatatctcattatgatcagtgccctcatggccctcgtattt atcaagtacctcccagaatggactgcatggctcatcttggctgtgatttcaatatacgat ttagtggctgttttgtgtccaaaaggtccacttcgtttgctggttgaaacagctcaggag agaaatgaaactctctttcccgctcttatttactcctcaaccatggtgtggttggtgaat atggcagaaggagacccagaggcccaaaggaaagtatccaaaaactccaattataatgca caaagcacagaaagtgagtcacaagaccctgtgacagagagtgacgatggcggcttcagt gaagagtgggaagcccagagggacagtcgcctaggacctcaccgctctacaactgagtca cgcgctgctgcacaggaactttccagcagcatcctagccagtgaggacccagaggaaagg ggagtaaagcttgggttaggagacttcattttctacagcgtgctggttggcaaggcttcc gcaacagccagtggggactggaacacaaccatagcctgctttgtagccatattgattggt ttgtgccttacattattactcctcgccattttcaagaaagcattgccagctcttccaatt tctatcacctttgggcttgttttctactttgccacagattatcttgtgcagccttttatg gaccaattagcattccatcagttttatgtctag

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