Neogale vison (American mink): 122901058 Help Entry 122901058         CDS       T08764                                  Symbol ACTR1A Name (RefSeq) alpha-centractin   KO K16575   centractin Organism nvs  Neogale vison (American mink) Pathway nvs04814   Motor proteins nvs05014   Amyotrophic lateral sclerosis nvs05016   Huntington disease nvs05022   Pathways of neurodegeneration - multiple diseases nvs05132   Salmonella infection Brite KEGG Orthology (KO) [BR:nvs00001]  09140 Cellular Processes   09142 Cell motility    04814 Motor proteins     122901058 (ACTR1A)  09160 Human Diseases   09171 Infectious disease: bacterial    05132 Salmonella infection     122901058 (ACTR1A)   09164 Neurodegenerative disease    05014 Amyotrophic lateral sclerosis     122901058 (ACTR1A)    05016 Huntington disease     122901058 (ACTR1A)    05022 Pathways of neurodegeneration - multiple diseases     122901058 (ACTR1A)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03036 Chromosome and associated proteins [BR:nvs03036]     122901058 (ACTR1A)   09183 Protein families: signaling and cellular processes    04812 Cytoskeleton proteins [BR:nvs04812]     122901058 (ACTR1A)    04147 Exosome [BR:nvs04147]     122901058 (ACTR1A) Chromosome and associated proteins [BR:nvs03036]  Eukaryotic type   Centrosome formation proteins    Microtubules and associated factors     Dynactin complex      122901058 (ACTR1A) Cytoskeleton proteins [BR:nvs04812]  Eukaryotic cytoskeleton proteins   Actin filaments / Microfilaments    Actins     Actin-related proteins      122901058 (ACTR1A) Exosome [BR:nvs04147]  Exosomal proteins   Exosomal proteins of bladder cancer cells    122901058 (ACTR1A) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Actin Motif Other DBs NCBI-GeneID:  122901058 NCBI-ProteinID:  XP_044096331 UniProt:  A0A8C7BGS3 LinkDB All DBs Position 2:complement(214211970..214231310) Genome browser AA seq 376 aa AA seqDB search MESYDVIANQPVVIDNGSGVIKAGFAGDQIPKYCFPNYVGRPKHVRVMAGALEGDIFIGP KAEEHRGLLSIRYPMEHGIVKDWNDMERIWQYVYSKDQLQTFSEEHPVLLTEAPLNPRKN RERAAEVFFETFNVPALFISMQAVLSLYATGRTTGVVLDSGDGVTHAVPIYEGFAMPHSI MRIDIAGRDVSRFLRLYLRKEGYDFHSSSEFEIVKAIKERACYLSINPQKDETLETEKAQ YYLPDGSTIEIGPSRFRAPELLFRPDLIGEESEGIHEVLVFAIQKSDMDLRRTLFSNIVL SGGSTLFKGFGDRLLSEVKKLAPKDVKIRISAPQERLYSTWIGGSILASLDTFKKMWVSK KEYEEDGARSIHRKTF NT seq 1131 nt NT seq  +upstreamnt  +downstreamnt atggagtcctacgatgtgatcgccaatcagcctgtcgtgatcgacaacggatctggtgtg attaaagctggttttgctggtgatcagattcccaaatactgctttccaaactatgtgggc agacccaaacacgttcgcgtcatggccggagcccttgaaggtgacatcttcattgggccc aaagccgaggaacaccgagggctgctgtccatccgctaccccatggaacatggcatcgtc aaggactggaatgacatggagcgcatctggcagtatgtctattccaaggaccagctgcag actttctctgaggagcatcctgtgctcctgacggaggcgcctttaaacccacggaaaaat cgcgaacgagcagctgaagttttcttcgagaccttcaatgtcccagcccttttcatctcc atgcaagctgtgctcagcctttacgccacaggccggaccacaggcgtggtgctggattct ggggatggtgtcacacatgctgtgcccatttatgagggctttgccatgccccactcaatt atgcgcatcgacatcgctggccgagatgtctctcgcttccttcgcctctacctgcggaag gagggctatgatttccactcatcgtccgagtttgagattgtcaaggccataaaagaaaga gcctgctacctgtccataaacccacagaaggatgagactctagagacggagaaagctcag tactacctgcccgacggcagcaccattgagattggtccttcccgattccgagcacctgag ctgctattcaggccagacctgatcggagaggaaagtgagggcatccatgaggtgctggtg tttgccatccagaagtcggacatggacctgcggcgcacacttttctcgaacattgtcctc tcaggaggctccaccctgttcaaaggtttcggtgacagactactgagtgaagtgaagaaa ctggctccgaaagacgtgaagataaggatatccgcacctcaggagaggctgtattccaca tggattgggggctccatcctcgcctccctggacacctttaagaagatgtgggtctccaag aaggaatatgaggaagacggtgcccgatctatccacaggaaaaccttctaa

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